2024 |
Child Opportunity Index: A Multidimensional Indicator to Measure Neighborhood Conditions Influencing Children's Health |
Articolo in rivista |
Go to |
2024 |
New and old criteria for diagnosing celiac disease: do they really differ? A retrospective observational study |
Articolo in rivista |
Go to |
2024 |
Cardiovascular involvement in children with COVID-19 temporally related multisystem inflammatory syndrome (MIS-C): can cardiac magnetic resonance arrive to the heart of the problem? |
Articolo in rivista |
Go to |
2024 |
Increased adherence to influenza vaccination among Palermo family pediatricians: a study on safety and compliance of qLAIV vaccination |
Articolo in rivista |
Go to |
2024 |
Manifestazioni cutanee anulari e lupus eritematoso neonatale |
Articolo in rivista |
Go to |
2024 |
Carnitine palmitoyltransferase II (CPT II) deficiency responsible for refractory cardiac arrhythmias, acute multiorgan failure and early fatal outcome |
Articolo in rivista |
Go to |
2023 |
Report and follow-up on two new patients with congenital mesoblastic nephroma |
Articolo in rivista |
Go to |
2023 |
Tubulointerstitial nephritis and uveitis syndrome post-COVID-19 |
Lettera |
Go to |
2023 |
Oligomenorrhea in two girls with familial mediterranean fever: how chronic inflammation can impair ovarian cycle |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2023 |
Growth and final height of adolescents with systemic juvenile idiopathic arthritis in the transitional age: a monocentric case series |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2023 |
MIS‑C and methylmalonic acidaemia. The role of anakinra to abate the cytokine storm |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2023 |
Lupus nephritis in childhood: the analysis of a cohort in the transitional age |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2023 |
The thousand faces of mevalonate kinase deficiency: a challenging case |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2023 |
Familial Behçet‑like autoinflammatory disease‑3 (AIFBL3), caused by heterozygous mutation in the rela gene: a case report |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2023 |
BD‑like disease associated with TNFAIP3 gene mutation: a case report |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2023 |
La Bioetica sul campo: una sfida per il neonatologo e il pediatra |
Articolo in rivista |
Go to |
2023 |
Un caso di pericardite recidivante colchicina-resistente |
Articolo in rivista |
Go to |
2023 |
A pediatric case of Chlamydia psittaci caused severe Acute Respiratory Distress Syndrome (ARDS) in Italy |
Articolo in rivista |
Go to |
2023 |
Advances for pediatricians in 2022: allergy, anesthesiology, cardiology, dermatology, endocrinology, gastroenterology, genetics, global health, infectious diseases, metabolism, neonatology, neurology, oncology, pulmonology |
Review essay (rassegna critica) |
Go to |
2023 |
Penile Length Assessment of Children Treated for Primary Buried Penis: Can Satisfying Penile Growth Always Be Achieved? |
Articolo in rivista |
Go to |
2023 |
UPDATE - 2022 Italian guidelines on the management of bronchiolitis in infants |
Review essay (rassegna critica) |
Go to |
2023 |
Year 2022: exploring COVID-19 pandemic in children |
Review essay (rassegna critica) |
Go to |
2023 |
Online "Sharenting": The Dangers of Posting Sensitive Information About Children on Social Media |
Review essay (rassegna critica) |
Go to |
2023 |
Federico II tra genetica ed epigenetica: il complesso dei “nonni” |
Articolo in rivista |
Go to |
2023 |
LESIONI DA “CAPELLO ATTORCIGLIATO” IN UN LATTANTE |
Articolo in rivista |
Go to |
2023 |
Intraoperative ultrasound-assisted endoscopic treatment of primary intermediate and high-grade vesicoureteral reflux in children in a long-term follow-up |
Articolo in rivista |
Go to |
2023 |
Safety of Rotavirus Vaccination in Preterm Infants Admitted in Neonatal Intensive Care Units in Sicily, Italy: A Multicenter Observational Study |
Articolo in rivista |
Go to |
2023 |
Follow-Up to Ensure Continuity of Care and Support Preventive Care |
Capitolo o Saggio |
Go to |
2023 |
Penile Length Assessment of Children Treated for Primary Buried Penis: Can Satisfying Penile Growth Always Be Achieved? |
Articolo in rivista |
Go to |
2023 |
Lo spettro dei disordini feto-alcolici: una guida
per il pediatra |
Articolo in rivista |
Go to |
2023 |
New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conception |
Articolo in rivista |
Go to |
2023 |
Ten-month follow-up of patients with covid-19 temporally related multi-system inflammatory syndrome in children: the experience of the children hospital of Palermo |
Articolo in rivista |
Go to |
2022 |
IL MITO DI EDIPO COME PARADIGMA DEL PROFUGO E DEL MIGRANTE |
Articolo in rivista |
Go to |
2022 |
LO SCORBUTO, SEGNALE DI ALLARME DI UN DISTURBO DELLO SPETTRO AUTISTICO |
Articolo in rivista |
Go to |
2022 |
Epstein-Barr virus-associated acute pancreatitis: a clinical report and review of literature |
Articolo in rivista |
Go to |
2022 |
Clinical and genetic approach in the characterization of newborns with anorectal malformation |
Articolo in rivista |
Go to |
2022 |
Interstitial deletions of chromosome 1p: novel 1p31.3p22.2 microdeletion in a newborn with craniosynostosis, coloboma and cleft palate, and review of the genomic and phenotypic profiles |
Articolo in rivista |
Go to |
2022 |
Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case report |
Articolo in rivista |
Go to |
2022 |
Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis |
Articolo in rivista |
Go to |
2022 |
Distal Arthrogryposis type 5 in an Italian family due to an autosomal dominant gain-of-function mutation of the PIEZO2 gene |
Articolo in rivista |
Go to |
2022 |
Novel de novo missense mutation in the interferon regulatory factor 6 gene in an Italian infant with IRF6-related disorder |
Articolo in rivista |
Go to |
2022 |
Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome |
Articolo in rivista |
Go to |
2022 |
Cutis verticis gyrata and Noonan syndrome: report of two cases with pathogenetic variant in SOS1 gene |
Articolo in rivista |
Go to |
2022 |
Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability |
Articolo in rivista |
Go to |
2022 |
Composition of Human Breast Milk Microbiota and Its Role in Children's Health |
Articolo in rivista |
Go to |
2022 |
Adequate Training and Multidisciplinary Support May Assist Pediatricians in Properly Handling and Managing Gender Incongruence and Dysphoria |
Articolo in rivista |
Go to |
2022 |
A novel NF1 mutation in a pediatric patient with renal artery aneurysm |
Articolo in rivista |
Go to |
2022 |
New insights in pediatrics in 2021: choices in allergy and immunology, critical care, endocrinology, gastroenterology, genetics, haematology, infectious diseases, neonatology, neurology, nutrition, palliative care, respiratory tract illnesses and telemedicine |
Review essay (rassegna critica) |
Go to |
2022 |
Quando l’amnios si rompe troppo presto e… da solo |
Articolo in rivista |
Go to |
2022 |
Epstein-Barr virus-associated acute pancreatitis: a clinical report and review of literature |
Articolo in rivista |
Go to |
2022 |
Cardio-facio-cutaneous syndrome and gastrointestinal defects: report on a newborn with 19p13.3 deletion including the MAP 2K2 gene |
Articolo in rivista |
Go to |
2022 |
DIAGNOSI PRECOCE DEI DISTURBI DELLO SPETTRO AUTISTICO: ESPERIENZA CLINICA E RUOLO DEI TEST GENETICI |
Articolo in rivista |
Go to |
2022 |
Febrile infection-related Epilepsy Syndrome (FIRES): a severe encephalopathy with status epilepticus. Literature review and presentation of two new cases |
Review essay (rassegna critica) |
Go to |
2022 |
Genetics and"democracy" |
Articolo in rivista |
Go to |
2022 |
Intestinal malrotation in a female newborn affected by Osteopathia Striata with Cranial Sclerosis due to a de novo heterozygous nonsense mutation of the AMER1 gene |
Articolo in rivista |
Go to |
2022 |
The Use of Social Media in Children and Adolescents: Scoping Review on the Potential Risks |
Articolo in rivista |
Go to |
2022 |
The awareness and acceptance of anti-COVID 19 vaccination in adolescence |
Articolo in rivista |
Go to |
2022 |
COVID 19 vaccine in the pediatric age: the recommendation of the Italian Pediatric Society |
Articolo in rivista |
Go to |
2022 |
The pandemic within the pandemic: the surge of neuropsychological disorders in Italian children during the COVID-19 era |
Articolo in rivista |
Go to |
2022 |
The year 2021 in COVID-19 pandemic in children |
Review essay (rassegna critica) |
Go to |
2022 |
Sensitivity of three commercial tests for SARS-CoV-2 serology in children: an Italian multicentre prospective study |
Articolo in rivista |
Go to |
2022 |
Congenital syphilis in a preterm newborn with gastrointestinal disorders and postnatal growth restriction |
Articolo in rivista |
Go to |
2022 |
Safety and efficacy of a probiotic-containing infant formula supplemented with 2'-fucosyllactose: a double-blind randomized controlled trial |
Articolo in rivista |
Go to |
2022 |
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome |
Articolo in rivista |
Go to |
2022 |
POSTERIOR FOSSA TUMORS: A CASE REPORT OF ACQUIRED TORTICOLLIS IN CHILDREN |
Articolo in rivista |
Go to |
2022 |
A refugee newborn with heart failure and initial hydrops: Diagnostic clues of spectral Doppler examinations |
Nota o commento |
Go to |
2022 |
I BAMBINI DELLA DIVINA COMMEDIA |
Articolo in rivista |
Go to |
2021 |
La Neonatologia ai tempi di JFK... |
Articolo in rivista |
Go to |
2021 |
Necrotizing enterocolitis in the preterm: newborns medical and nutritional Management in a Single-Center Study |
Articolo in rivista |
Go to |
2021 |
Shotgun Proteomics of Isolated Urinary Extracellular Vesicles for Investigating Respiratory Impedance in Healthy Preschoolers |
Articolo in rivista |
Go to |
2021 |
Revised recommendations of the Italian Society of Pediatrics about the general management of Kawasaki disease |
Review essay (rassegna critica) |
Go to |
2021 |
Smartphone use and addiction during the coronavirus disease 2019 (COVID-19) pandemic: cohort study on 184 Italian children and adolescents |
Articolo in rivista |
Go to |
2021 |
Recommendations for neonatologists and pediatricians working in first level birthing centers on the first communication of genetic disease and malformation syndrome diagnosis: consensus issued by 6 Italian scientific societies and 4 parents’ associations |
Articolo in rivista |
Go to |
2021 |
LA DIAGNOSI DI IPOTIROIDISMO CONGENITO AI TEMPI DELLA PANDEMIA DA SARS-CoV-2: L’ESPERIENZA DELLA CLINICA PEDIATRICA DI PALERMO |
Abstract in atti di convegno pubblicato in volume |
Go to |
2021 |
Jacobsen syndrome and neonatal bleeding: report on two unrelated patients |
Articolo in rivista |
Go to |
2021 |
Novel missense mutation of the TP63 gene in a newborn with Hay-Wells/Ankyloblepharon-Ectodermal defects-Cleft lip/palate (AEC) syndrome: clinical report and follow-up |
Articolo in rivista |
Go to |
2021 |
Nuovi percorsi e modalità assistenziali nel follow up di pazienti con deficit di GH in trattamento sostitutivo durante la pandemia da Sars Cov2 |
Abstract in atti di convegno pubblicato in volume |
Go to |
2021 |
SAIApp: a web application of the university of palermo dedicated to children with autoinflammatory syndromes |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2021 |
PROGETTO DI SMART WORKING DURANTE LA PANDEMIA DI COVID-19: SMART CO-WORKING PER LA RETE ASSISTENZIALE FRA PEDIATRI DI LIBERA SCELTA E UN CENTRO DI RIFERIMENTO IN SICILIA PER L’IPOTIROIDISMO CONGENITO |
Abstract in atti di convegno pubblicato in volume |
Go to |
2021 |
Scurvy as an alarm bell of autistic spectrum disorder in the first world: A case report of a 3-year-old girl |
Articolo in rivista |
Go to |
2021 |
CASO CLINICO: triplicazione del gene SHOX in un paziente con disgenesia gonadica mista e mosaicismo 46,X,i(Y)(p10)[94]/45,X[13] |
Abstract in atti di convegno pubblicato in volume |
Go to |
2021 |
Analysis of risk and prognostic factors in a population of pediatric patients hospitalized for acute malnutrition at the Chiulo hospital, Angola |
Articolo in rivista |
Go to |
2021 |
2q13 microdeletion syndrome: Report on a newborn with additional features expanding the phenotype |
Articolo in rivista |
Go to |
2021 |
Novel SCNN1A gene splicing-site mutation causing autosomal recessive pseudohypoaldosteronism type 1 (PHA1) in two Italian patients belonging to the same small town |
Articolo in rivista |
Go to |
2021 |
Educational interventions on pregnancy vaccinations during childbirth classes improves vaccine coverages among pregnant women in Palermo’s province |
Articolo in rivista |
Go to |
2021 |
Neonatal screening for congenital hypothyroidism in an Italian Centre: a 5-years real-life retrospective study |
Articolo in rivista |
Go to |
2021 |
School in Italy: a safe place for children and adolescents |
Articolo in rivista |
Go to |
2021 |
Social media use to improve communication on children and adolescent’s health: the role of the Italian Paediatric Society influencers |
Articolo in rivista |
Go to |
2021 |
SAIApp: un'app dell'Università di Palermo dedicata ai bambini con malattie autoinfiammatorie |
Abstract in atti di convegno pubblicato in volume |
Go to |
2021 |
Pediatric routine vaccinations in the COVID 19 lockdown period: the survey of the Italian Pediatric Society |
Articolo in rivista |
Go to |
2021 |
Prevention and contrast of child abuse and neglect in the practice of European paediatricians: a multi-national pilot study |
Articolo in rivista |
Go to |
2021 |
Inter-society consensus for the use of inhaled corticosteroids in infants, children and adolescents with airway diseases |
Articolo in rivista |
Go to |
2021 |
Un caso di malattia di Kawasaki refrattaria |
Abstract in atti di convegno pubblicato in volume |
Go to |
2021 |
Artrite o artropatia? Nuova mutazione del gene GNPTG in bambina con mucolipidosi IIIγ |
Abstract in atti di convegno pubblicato in volume |
Go to |
2021 |
From Neonatal Intensive Care to Neurocritical Care: Is It Still a Mirage? The Sicilian Multicenter Project |
Articolo in rivista |
Go to |
2021 |
Developments in pediatrics in 2020: choices in allergy, autoinflammatory disorders, critical care, endocrinology, genetics, infectious diseases, microbiota, neonatology, neurology, nutrition, ortopedics, respiratory tract illnesses and rheumatology |
Articolo in rivista |
Go to |
2021 |
Breastfeeding and COVID-19 vaccination: position statement of the Italian scientific societies |
Articolo in rivista |
Go to |
2021 |
Epidemiology, Clinical Features and Prognostic Factors of Pediatric SARS-CoV-2 Infection: Results From
an Italian Multicenter Study |
Articolo in rivista |
Go to |
2021 |
The social role of pediatrics in the past and present times |
Lettera |
Go to |
2021 |
Cocleo-labirintopatie nel bambino. Come non perdere l'equilibrio. |
Articolo in rivista |
Go to |
2021 |
Prognostic factors and predictors of outcome in children with autism spectrum disorder: the role of the paediatrician |
Articolo in rivista |
Go to |
2021 |
Effects of Coronavirus Disease 2019 (COVID-19) on Family Functioning |
Articolo in rivista |
Go to |
2021 |
Children Witnessing Domestic and Family Violence: A Widespread Occurrence during the Coronavirus Disease 2019 (COVID-19) Pandemic |
Articolo in rivista |
Go to |
2021 |
Increased Exposure to Violence and Risk of Neurodevelopmental Disorders in Children |
Articolo in rivista |
Go to |
2021 |
First report of X-linked hypohidrotic ectodermal dysplasia with a hemizygous c.1142G > C in the EDA gene: variant of uncertain significance or new pathogenic variant? |
Articolo in rivista |
Go to |
2021 |
Macronutrient balance and micronutrient amounts through growth and development |
Review essay (rassegna critica) |
Go to |
2021 |
Ocular Motor Paroxysmal Events in Neonates and Infants: A Review of the Literature |
Articolo in rivista |
Go to |
2021 |
The Dark Side of the Web-A Risk for Children and Adolescents Challenged by Isolation during the Novel Coronavirus 2019 Pandemic |
Articolo in rivista |
Go to |
2021 |
Lesioni cutanee stellate e simmetriche in un gemello “rimasto solo” |
Articolo in rivista |
Go to |
2021 |
Il neonato che “sa di sale” |
Articolo in rivista |
Go to |
2021 |
THE “SALT-TASTING” NEWBORN |
Articolo in rivista |
Go to |
2021 |
Efficacy of a coordinated strategy for containment of multidrug-resistant Gram-negative bacteria carriage in a Neonatal Intensive Care Unit in the context of an active surveillance program |
Articolo in rivista |
Go to |
2020 |
Indagare cum “granuloma” salis: malattia granulomatosa cronica vs malattia di Crohn |
Articolo in rivista |
Go to |
2020 |
Chromosome 15q BP4-BP5 Deletion in a Girl with Nocturnal Frontal Lobe Epilepsy, Migraine, Circumscribed Hypertrichosis, and Language Impairment |
Articolo in rivista |
Go to |
2020 |
Non era una MICI |
Articolo in rivista |
Go to |
2020 |
Lacune neonatali: l’aplasia cutis congenita |
Articolo in rivista |
Go to |
2020 |
Congenital pelvic skeletal anomalies: Clinical and radiographic evaluation of newborns with gastrointestinal malformation |
Articolo in rivista |
Go to |
2020 |
Recognizable neonatal clinical features of aplasia cutis congenita |
Articolo in rivista |
Go to |
2020 |
Delayed neonatal visual evoked potentials are associated to asymmetric growth pattern in twins |
Articolo in rivista |
Go to |
2020 |
Neonatal ten-year retrospective study on neural tube defects in a second level University Hospital |
Articolo in rivista |
Go to |
2020 |
Growth patterns and associated risk factors of congenital malformations in twins |
Articolo in rivista |
Go to |
2020 |
Comparison of Postural Features and Muscle Strength between Children with Idiopathic Short Stature and Healthy Peers in Relation to Physical Exercise |
Articolo in rivista |
Go to |
2020 |
Infant developmental profile of Crisponi syndrome due to compound heterozygosity for CRLF1 deletion |
Articolo in rivista |
Go to |
2020 |
Neonatal deficiency: Congenital skin aplasia |
Articolo in rivista |
Go to |
2020 |
FMF is not always "fever": from clinical presentation to "treat to target" |
Review essay (rassegna critica) |
Go to |
2020 |
The child with overgrowth between clinical variability and genetic heterogeneity |
Articolo in rivista |
Go to |
2020 |
A refugee newborn with heart failure and initial hydrops: Diagnostic clues of spectral Doppler examinations |
Nota o commento |
Go to |
2020 |
Current Insights on Early Life Nutrition and Prevention of Allergy |
Articolo in rivista |
Go to |
2020 |
MACROCEPHALY FROM A NORMAL VARIANT TO A THREATENING CONDITION. A SINGLE CENTER RETROSPECTIVE STUDY ON 189 SUBJECTS |
Articolo in rivista |
Go to |
2020 |
Identification of bronchiolitis profiles in Italian children through the application of latent class analysis |
Articolo in rivista |
Go to |
2020 |
LARGE FOR GESTATIONAL AGE, MACROSOMIA, OVERGROWTH: AN UPDATE ON
DEFINITIONS AND DETERMINANTS |
Articolo in rivista |
Go to |
2020 |
Total colonic aganglionosis and cleft palate in a newborn with Janus-cysteine 618 mutation of RET proto-oncogene: A case report |
Articolo in rivista |
Go to |
2020 |
Candida thrombophlebitis in children: A systematic review of the literature |
Articolo in rivista |
Go to |
2020 |
Upper and lower limb strength and body posture in children with congenital hypothyroidism: An observational case-control study |
Articolo in rivista |
Go to |
2020 |
A novel cct5 missense variant associated with early onset motor neuropathy |
Articolo in rivista |
Go to |
2020 |
Autosomal recessive polycystic kidney disease: case report of a newborn with rare PKHD1 mutation, rapid renal enlargement and early fatal outcome |
Articolo in rivista |
Go to |
2020 |
Una anoressia “infiammatoria” |
Articolo in rivista |
Go to |
2020 |
To investigate cum “granuloma” salis: Chronic granulomatous disease vs Crohn's disease |
Articolo in rivista |
Go to |
2020 |
From smart working to smart co-working in the covid-19 era: a pilot program of cooperation around autoinflammatory diseases |
Poster pubblicato in rivista |
Go to |
2020 |
Novel LRPPRC compound heterozygous mutation in a child with early-onset Leigh syndrome French-Canadian type: Case report of an Italian patient |
Articolo in rivista |
Go to |
2020 |
Neonatal hyperinsulinemic hypoglycemia: Case report of kabuki syndrome due to a novel KMT2D splicing-site mutation |
Articolo in rivista |
Go to |
2020 |
A novel GABRB3 variant in Dravet syndrome: Case report and literature review |
Articolo in rivista |
Go to |
2020 |
Typical Kawasaki disease with atypical pneumonia: a paediatric case report |
Lettera |
Go to |
2020 |
Spider bite mimicking pyoderma gangrenosum in sJIA: a case report |
Poster pubblicato in rivista |
Go to |
2020 |
Brainstem Auditory Evoked Potentials and Visual Potentials in Kawasaki Disease: An Observational Monocentric Study |
Articolo in rivista |
Go to |
2020 |
Ketogenic diet for infants with epilepsy: A literature review |
Articolo in rivista |
Go to |
2020 |
The Italian paediatric society raccomandations on children and adolescents extra-domestic activities during the SARS COV-2 emergency phase 2 |
Articolo in rivista |
Go to |
2020 |
N-BiPAP vs n-CPAP in term neonate with respiratory distress syndrome |
Articolo in rivista |
Go to |
2020 |
The Hikikomori Phenomenon of Social Withdrawal: An Emerging Condition Involving Youth's Mental Health and Social Participation |
Articolo in rivista |
Go to |
2020 |
Epidemiology of enuresis: a large number of children at risk of low regard |
Articolo in rivista |
Go to |
2020 |
Children with special health care needs attending emergency department in Italy: analysis of 3479 cases |
Articolo in rivista |
Go to |
2020 |
Kawasaki disease epidemic: pitfalls |
Articolo in rivista |
Go to |
2020 |
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 |
Articolo in rivista |
Go to |
2020 |
The Health Risks of Electronic Cigarettes Use in Adolescents |
Articolo in rivista |
Go to |
2020 |
What's the name? Weight stigma and the battle against obesity |
Articolo in rivista |
Go to |
2020 |
West syndrome: a comprehensive review |
Articolo in rivista |
Go to |
2020 |
Facial masks in children: the position statement of the Italian pediatric society |
Nota o commento |
Go to |
2020 |
Chromosome 15q BP3 to BP5 deletion is a likely locus for speech delay and language impairment: Report on a four-member family and an unrelated boy |
Articolo in rivista |
Go to |
2020 |
Ventilation, oxidative stress and risk of brain injury in preterm newborn |
Articolo in rivista |
Go to |
2020 |
Multicentre Italian study of SARS-CoV-2 infection in children and adolescents, preliminary data as at 10 April 2020 |
Articolo in rivista |
Go to |
2020 |
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures |
Articolo in rivista |
Go to |
2020 |
What is the impact of a novel MED12 variant on syndromic conotruncal heart defects? Analysis of case report on two male sibs |
Articolo in rivista |
Go to |
2020 |
Providing pediatric well-care and sick visits in the COVID-19 pandemic era: the recommendations of the Italian pediatric society |
Articolo in rivista |
Go to |
2020 |
Advances in paediatrics in 2019: current practices and challenges in allergy, endocrinology, gastroenterology, public health, neonatology, nutrition, nephrology, neurology, respiratory diseases and rheumatic diseases |
Articolo in rivista |
Go to |
2020 |
Best practices, challenges and innovations in pediatrics in 2019 |
Articolo in rivista |
Go to |
2020 |
BAMBINI E CORONAVIRUS: LA DOVEROSA RICERCA DI UN EQUILIBRIO TRA I PRESUNTI RISCHI E I DOCUMENTATI DANNI COLLATERALI |
Articolo in rivista |
Go to |
2019 |
Il neonato a colori: le sfumature di grigio |
Articolo in rivista |
Go to |
2019 |
Methemoglobinemia Associated with Late-Onset Neonatal Sepsis: A Single-Center Experience |
Articolo in rivista |
Go to |
2019 |
UN OMBELICO…TROPPO SPESSO BAGNATO |
Articolo in rivista |
Go to |
2019 |
7q31.32 partial duplication: First report of a child with dysmorphism, autistic spectrum disorder, moderate intellectual disability and, epilepsy. Literature review |
Review essay (rassegna critica) |
Go to |
2019 |
Il neonato a colori: nero a metà |
Articolo in rivista |
Go to |
2019 |
Il neonato a colori: rosso
A proposito di “eritrodermia ittiosiforme congenita” |
Articolo in rivista |
Go to |
2019 |
A novel mutation in KCNQ3-related benign familial neonatal epilepsy: electroclinical features and neurodevelopmental outcome |
Articolo in rivista |
Go to |
2019 |
Early Treatment of Systemic Juvenile Idiopathic Arthritis with Canakinumab and Complete Remission After 2 Years of Treatment Suspension: Case Report of an Adolescent Girl |
Articolo in rivista |
Go to |
2019 |
Kawasaki disease triggered by parvovirus infection: An atypical case report of two siblings |
Articolo in rivista |
Go to |
2019 |
IPEREOSINOFILIA IN MALATTIA DI KAWASAKI: INDICE DI RISCHIO DI PATOLOGIA CARDIACA IN UNA CASISTICA PEDIATRICA SICILIANA |
Abstract in atti di convegno pubblicato in volume |
Go to |
2019 |
Fetal growth restriction: A growth pattern with fetal, neonatal and long-term consequences |
Review essay (rassegna critica) |
Go to |
2019 |
GH successful treatment in a female with a de novo 46,XX,add(X)(p36),t(X;Y)(p36.3;p11.2), growth impairment and SHOX-haploinsufficiency |
Lettera |
Go to |
2019 |
DELEZIONE CROMOSOMICA CRIPTICA 1p31.1: EFFICACIA DELLA TERAPIA COMBINATA CON L-TIROXINA, GH ED LHRHa PER MIGLIORARE LA PROGNOSI STATURALE |
Abstract in atti di convegno pubblicato in volume |
Go to |
2019 |
VARIABILITA’ INTRA-FAMILIARE FENOTIPICA E SULLA STATURA DEFINITIVA NELL’APLOINSUFFICIENZA DEL GENE SHOX |
Abstract in atti di convegno pubblicato in volume |
Go to |
2019 |
Aspergillosi polmonare in soggetto con lupus eritematoso sistemico e sindrome da attivazione macrofagica |
Abstract in atti di convegno pubblicato in volume |
Go to |
2019 |
EDEMA EMORRAGICO ACUTO DELL'INFANZIA: UN CASE REPORT |
Abstract in atti di convegno pubblicato in volume |
Go to |
2019 |
The correlation of functional pain and psychological distress: A study in Italian school students |
Articolo in rivista |
Go to |
2019 |
MVK E DEFICIT ACCRESCITIVO IN BAMBINA NATA SGA |
Abstract in atti di convegno pubblicato in volume |
Go to |
2019 |
PAPA and FMF in two siblings: possible amplification of clinical presentation? A case report |
Articolo in rivista |
Go to |
2019 |
Congenital emphysematous lung disease associated with a novel Filamin A mutation. Case report and literature review |
Articolo in rivista |
Go to |
2019 |
MIASTENIA GRAVIS ED ESOFAGITE EOSINOFILA IN ADOLESCENTE CON LES |
Abstract in atti di convegno pubblicato in volume |
Go to |
2019 |
New insights in respiratory impedance in young children after repair of congenital diaphragmatic hernia: a cross-sectional study. |
Lettera |
Go to |
2019 |
MALATTIA DI KAWASAKI ATIPICA |
Abstract in atti di convegno pubblicato in volume |
Go to |
2019 |
MALATTIA DI KAWASAKI E MAS INDOTTA DA INFEZIONE DA EBV IN PAZIENTE CON LINFOISTIOCITOSI EMOFAGOCITICA DI TIPO 2 |
Abstract in atti di convegno pubblicato in volume |
Go to |
2019 |
SHOX HAPLOINSUFFICIENCY INTRA FAMILIAL PHENOTIPIC VARIABILITY AND THE IMPACT ON FINAL HEIGHT: REPORT OF A PEDIGREE |
Poster pubblicato in rivista |
Go to |
2019 |
The role of physical activity on postural stability and fitness characteristics in pediatric patients with GH deficiency |
Poster pubblicato in rivista |
Go to |
2019 |
Shox-Haploinsufficiency Intra-Familial Phenotipic Variability and The Impact On Final Height: Report of a Pedigree |
Poster pubblicato in rivista |
Go to |
2019 |
The role of physical activity on postural stability and fitness characteristics in pediatric patients with GH deficiency |
Poster pubblicato in rivista |
Go to |
2019 |
Do children and adolescents with idiopathic short stature show postural alterations? Possible influence of SHOX haploinsufficiency in a pilot study |
Poster pubblicato in rivista |
Go to |
2019 |
What Is the Impact of Innovative Electronic Health Interventions in Improving Treatment Adherence in Asthma? The Pediatric Perspective. |
Articolo in rivista |
Go to |
2019 |
Familial Mediterranean Fever: An unusual cause of liver disease |
Articolo in rivista |
Go to |
2019 |
Kawasaki disease triggered by EBV virus in a child with Familial Mediterranean Fever |
Articolo in rivista |
Go to |
2019 |
Physical, psychological and social impact of school violence on children |
Articolo in rivista |
Go to |
2019 |
Perinatal and newborn care in a two years retrospective study in a first level peripheral hospital in Sicily (Italy) |
Articolo in rivista |
Go to |
2019 |
Media use during adolescence: the recommendations of the Italian Pediatric Society. |
Articolo in rivista |
Go to |
2019 |
Report on advances for pediatricians in 2018: allergy, cardiology, critical care, endocrinology, hereditary metabolic diseases, gastroenterology, infectious diseases, neonatology, nutrition, respiratory tract disorders and surgery. |
Review essay (rassegna critica) |
Go to |
2019 |
Molecular Mechanism Involved in the Pathogenesis of Early-Onset Epileptic Encephalopathy |
Articolo in rivista |
Go to |
2019 |
Management of chronic urticaria in children: a clinical guideline |
Articolo in rivista |
Go to |
2019 |
CASO CLINICO: CARCINOMA TIROIDEO ASSOCIATO A IPERTIROIDISMO IN ETÀ PEDIATRICA: UNA RARA ASSOCIAZIONE |
Poster pubblicato in volume |
Go to |
2019 |
Childhood Dietary Intake in Italy: The Epidemiological "MY FOOD DIARY" Survey. |
Articolo in rivista |
Go to |
2019 |
Standard and Specialized Infant Formulas in Europe: Making, Marketing, and Health Outcomes |
Review essay (rassegna critica) |
Go to |
2019 |
STATURA DEFINITIVA NELL’APLOINSUFFICIENZA DEL GENE SHOX: VARIABILITA’ INTRA-FAMILIARE |
Poster pubblicato in volume |
Go to |
2019 |
Short-Term Neurodevelopmental Outcome in Term Neonates Treated with Phenobarbital versus Levetiracetam: A Single-Center Experience |
Articolo in rivista |
Go to |
2019 |
CASO CLINICO: L’UTILIZZO DELL’ORMONE DELLA CRESCITA IN SOGGETTO CON SINDROME DA MICRODELEZIONE E SBILANCIAMENTO CROMOSOMICO (CR3-6) |
Poster pubblicato in volume |
Go to |
2019 |
Influenza vaccination: opinions of health care professionals working in pediatric emergency departments. |
Articolo in rivista |
Go to |
2019 |
Preterm birth: seven-year retrospective study in a single centre population |
Articolo in rivista |
Go to |
2019 |
EFFETTI AVVERSI NEI PAZIENTI IN TERAPIA CON GH IN UN CENTRO PEDIATRICO: DATI REAL LIFE |
Poster pubblicato in volume |
Go to |
2019 |
PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation? |
Articolo in rivista |
Go to |
2019 |
General Movements (GMs): assessment and predictive value |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2019 |
High mobility group box 1 and markers of oxidative stress in human cord blood. |
Articolo in rivista |
Go to |
2019 |
Survey of Italian pediatricians on awareness, experiences and beliefs regarding direct-to-consumer genetic testing in minors |
Articolo in rivista |
Go to |
2019 |
Role of oxidative stress in neonatal respiratory distress syndrome |
Articolo in rivista |
Go to |
2019 |
Sportomics: metabolomics applied to sports. The new revolution? |
Articolo in rivista |
Go to |
2019 |
Microcephaly/Trigonocephaly, Intellectual Disability, Autism Spectrum Disorder, and Atypical Dysmorphic Features in a Boy with Xp22.31 Duplication |
Articolo in rivista |
Go to |
2019 |
Apnea events in neonatal age: A case report and literature review. |
Articolo in rivista |
Go to |
2019 |
The impact of genetic diseases on neonatal and pediatric care |
Articolo in rivista |
Go to |
2019 |
Microcephaly and macrocephaly. A study on anthropometric and clinical data from 308 subjects |
Articolo in rivista |
Go to |
2019 |
NF1 microdeletion syndrome: Case report of two new patients |
Articolo in rivista |
Go to |
2019 |
Il neonato a colori: bianco |
Articolo in rivista |
Go to |
2018 |
Il neonato a colori: a strisce colorate (Arlecchino) |
Articolo in rivista |
Go to |
2018 |
Esophageal atresia and Beckwith–Wiedemann syndrome in one of the naturally conceived discordant newborn twins: first report |
Articolo in rivista |
Go to |
2018 |
Transitional hemodynamics in infants of diabetic mothers by targeted neonatal echocardiography, electrocardiography and peripheral flow study |
Articolo in rivista |
Go to |
2018 |
Etiological heterogeneity and clinical variability in newborns with esophageal atresia |
Articolo in rivista |
Go to |
2018 |
Clinical cardiac assessment in newborns with prenatally diagnosed intrathoracic masses |
Articolo in rivista |
Go to |
2018 |
Clinical and molecular characterization of 112 single-center patients with Neurofibromatosis type 1 |
Articolo in rivista |
Go to |
2018 |
A Case of Cardiomyopathy Due to Premature Ductus Arteriosus Closure: The Flip Side of Paracetamol |
Articolo in rivista |
Go to |
2018 |
Exposure to Gastric Acid Inhibitors Increases the Risk of Infection in Preterm Very Low Birth Weight Infants but Concomitant Administration of Lactoferrin Counteracts This Effect |
Articolo in rivista |
Go to |
2018 |
WIDENING THE SCOPE OF NEXT GENERATION SEQUENCING APPLICATIONS IN PEDIATRIC MEDICAL GENETICS |
Articolo in rivista |
Go to |
2018 |
An unusual association of left-sided gastroschisis and persistent right umbilical vein |
Articolo in rivista |
Go to |
2018 |
Kawasaki disease: Guidelines of the Italian Society of Pediatrics, part i - Definition, epidemiology, etiopathogenesis, clinical expression and management of the acute phase |
Articolo in rivista |
Go to |
2018 |
Improvement of treatment adherence with growth hormone by easypod™ device: Experience of an Italian centre |
Articolo in rivista |
Go to |
2018 |
Kawasaki disease: Guidelines of Italian Society of Pediatrics, part II - Treatment of resistant forms and cardiovascular complications, follow-up, lifestyle and prevention of cardiovascular risks |
Articolo in rivista |
Go to |
2018 |
Chronic spontaneous urticaria or autoinflammatory disease? The therapeutic effect of omalizumab in a pediatric patient |
Articolo in rivista |
Go to |
2018 |
Intestinal Involvement in Kawasaki Disease |
Articolo in rivista |
Go to |
2018 |
Case–control study on intestinal intussusception: implications for anti-rotavirus vaccination |
Articolo in rivista |
Go to |
2018 |
Acute renal insufficiency and pancreatitis in a child with atypical Henoch–Schönlein purpura: efficacy of a single dose of cyclophosphamide |
Articolo in rivista |
Go to |
2018 |
SINDROME DA ATTIVAZIONE MACROFAGICA SECONDARIA AD IMMUNODEFICIT |
Abstract in atti di convegno pubblicato in volume |
Go to |
2018 |
LO SCREENING PER L’IPOTIROIDISMO CONGENITO: DATI RETROSPETTIVI DEGLI ULTIMI 5 ANNI IN UN SINGOLO CENTRO |
Abstract in atti di convegno pubblicato in volume |
Go to |
2018 |
UNA MALATTIA DI KAWASAKI AD ESORDIO MOLTO PRECOCE |
Abstract in atti di convegno pubblicato in volume |
Go to |
2018 |
LA PANCREATITE ACUTA: UNA TEMIBILE COMPLICANZA IN CORSO DI PORPORA DI HENOCHSCHONLEIN. CASISTICA DELLA CLINICA PEDIATRICA DI PALERMO |
Abstract in atti di convegno pubblicato in volume |
Go to |
2018 |
LO STUDIO DEI POTENZIALI EVOCATI VISIVI E UDITIVI IN PAZIENTI CON MALATTIA DI KAWASAKI: CASISTICA DELLA CLINICA PEDIATRICA DI PALERMO |
Abstract in atti di convegno pubblicato in volume |
Go to |
2018 |
INSIDIE DIAGNOSTICHE DELLA TROMBOSI VENOSA CEREBRALE: STORIA DI UN CASO CLINICO |
Abstract in atti di convegno pubblicato in volume |
Go to |
2018 |
DUE FRATELLI, IL PARVOVIRUS E DUE KAWASAKI CON FENOTIPO ATIPICO |
Abstract in atti di convegno pubblicato in volume |
Go to |
2018 |
The predictive role of pelvic magnetic resonance in the follow up of spontaneous or induced puberty in turner syndrome |
Articolo in rivista |
Go to |
2018 |
SHOX Haploinsufficiency in Short and Not Short Children: A Sigle Italian Cetre Data |
Poster pubblicato in rivista |
Go to |
2018 |
Efficacy of Mecasermin Treatment and Long-Term Survival in a Child with Leprechaunism |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2018 |
The Congenital Hypothyroidism Screening Programme in a Sigle Italian Centre: A 5-Years Retrospective Study |
Poster pubblicato in rivista |
Go to |
2018 |
Active immunization status against measles, mumps, rubella, hepatitis B in internationally adopted children, surveyed at the university hospital of Palermo, Sicily |
Articolo in rivista |
Go to |
2018 |
ARTRITE IDIOPATICA GIOVANILE E FITNESS: UN LAVORO DI SQUADRA |
Abstract in atti di convegno pubblicato in volume |
Go to |
2018 |
SINDROME DA ENCEFALOPATIA POSTERIORE REVERSIBILE: TEMIBILE COMPLICANZA IN CORSO DI MAS DA AIG SISTEMICA |
Abstract in atti di convegno pubblicato in volume |
Go to |
2018 |
NON SOLO PORPORA… SUCCESSO DELLA STRATEGIA TERAPEUTICA E NUTRIZIONALE |
Abstract in atti di convegno pubblicato in volume |
Go to |
2018 |
PANCREATITIS IN HENOCH-SCHONLEIN PURPURA. A SINGLE CENTRE OBSERVATIONAL STUDY |
Poster pubblicato in rivista |
Go to |
2018 |
JUVENILE IDIOPATHIC ARTHRITIS AND FITNESS: A TEAMWORK |
Poster pubblicato in rivista |
Go to |
2018 |
ISOLATED PYODERMA GANGRENOSUM AND ADALIMUMAB:CASE REPORT IN PAEDIATRIC AGE |
Poster pubblicato in rivista |
Go to |
2018 |
PARVOVIRUS INFECTION AND KAWASAKI DISEASE: ONE DISEASE FOR TWO SIBLINGS |
Poster pubblicato in rivista |
Go to |
2018 |
AUDITORY EVOKED POTENTIALS AND VISUAL EVOKED POTENTIALS: A HELPFUL TEST IN THE DIAGNOSIS AND FOLLOW UP OF KAWASAKI DISEASE |
Poster pubblicato in rivista |
Go to |
2018 |
Current status of laboratory and imaging diagnosis of neonatal necrotizing enterocolitis |
Articolo in rivista |
Go to |
2018 |
Mandatory vaccinations in European countries, undocumented information, false news and the impact on vaccination uptake: the position of the Italian pediatric society. |
Articolo in rivista |
Go to |
2018 |
The future outlook on allergen immunotherapy in children: 2018 and beyond. |
Review essay (rassegna critica) |
Go to |
2018 |
Advances in pediatrics in 2017: current practices and challenges in allergy, endocrinology, gastroenterology, genetics, immunology, infectious diseases, neonatology, nephrology, neurology, pulmonology from the perspective of Italian Journal of Pediatrics. |
Articolo in rivista |
Go to |
2018 |
Vitamin D in pediatric age: consensus of the Italian Pediatric Society and the Italian Society of Preventive and Social Pediatrics, jointly with the Italian Federation of Pediatricians. |
Review essay (rassegna critica) |
Go to |
2018 |
Guideline on management of the acute asthma attack in children by Italian Society of Pediatrics. |
Articolo in rivista |
Go to |
2018 |
Media devices in pre-school children: the recommendations of the Italian pediatric society |
Articolo in rivista |
Go to |
2018 |
Benign and severe early-life seizures: a round in the first year of life. |
Articolo in rivista |
Go to |
2018 |
Gambling disorder in adolescents: what do we know about this social problem and its consequences? |
Articolo in rivista |
Go to |
2018 |
Symptomatic seizures in preterm newborns: a review on clinical features and prognosis |
Review essay (rassegna critica) |
Go to |
2018 |
Cyberbullying a modern form of bullying: let's talk about this health and social problem. |
Articolo in rivista |
Go to |
2018 |
SLIT’s Prevention of the Allergic March |
Articolo in rivista |
Go to |
2018 |
An Appeal for Implementing Social Assistance and Welfare Programs for European Children Challenged by Parental Loss. |
Articolo in rivista |
Go to |
2018 |
Murdered women’s children: A social emergency and gloomy reality |
Articolo in rivista |
Go to |
2018 |
Il neonato a colori: blu, giallo-verde |
Articolo in rivista |
Go to |
2017 |
Bambini, soprattutto: storia di bambini-migranti dei nostri giorni |
Articolo in rivista |
Go to |
2017 |
Levetiracetam in Neonatal Seizures as First-line Treatment: A Prospective Study |
Articolo in rivista |
Go to |
2017 |
Terapia con inibitori dell'IL-1 in pazienti con mutazioni di malattie autoinfiammatorie a bassa penetranza: una casistica dall'età pediatrica al giovane adulta tra Sicilia e Toscana |
Abstract in atti di convegno pubblicato in volume |
Go to |
2017 |
Impact of Candida species colonization and azoles resistance in a neonatal intensive care unit |
eedings |
Go to |
2017 |
Efficacia di Omalizumab in una bambina con sindrome autoinfiammatoria e orticaria cronica |
Abstract in atti di convegno pubblicato in volume |
Go to |
2017 |
Patologia Muscolare Autoimmune: dermatomiosite. La nostra casistica. |
Poster pubblicato in volume |
Go to |
2017 |
Genotyping and antifungal susceptibility of Dipodascus capitatus isolated in a neonatal intensive care unit of a sicilian hospital |
Capitolo o Saggio |
Go to |
2017 |
Systemic lupus erythematosus and bullous pemphigoid with dramatic response to dapsone |
Articolo in rivista |
Go to |
2017 |
Coronary Artery Fistula in Down Syndrome: A Hidden Association |
Articolo in rivista |
Go to |
2017 |
Dilated azygos arch mimicking an aortic arch anomaly during thoracic surgery |
Articolo in rivista |
Go to |
2017 |
Preclinical Morphofunctional Alterations of Large Arteries in Children and Adolescent with Type 1 Diabetes Mellitus: Preliminary Data |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2017 |
POTENZIALI EVOCATI VISIVI DA FLASH IN GEMELLI IN EPOCA NEONATALE. CORRELAZIONI CON LA ADEGUATEZZA DEL PESO CON LA ETA' GESTAZIONALE (AGA VS SGA) |
eedings |
Go to |
2017 |
IPOGLICEMIA NEONATALE: RILIEVI EPIDEMIOLOGICI IN UN CAMPIONE DI NEONATI RICOVERATI (2012-2017) |
Poster non pubblicato |
Go to |
2017 |
Evaluation of Fitness and the Balance Levels of Children with a Diagnosis of Juvenile Idiopathic Arthritis: A Pilot Study |
Articolo in rivista |
Go to |
2017 |
Atypical presentation of anti-N-methyl-D-aspartate receptor encephalitis: Two case reports |
Articolo in rivista |
Go to |
2017 |
Effects of physical activity on postural balance in children with juvenile idiopathic arthritis: results from a pilot study |
Abstract in rivista |
Go to |
2017 |
Effetti dell'attività fisica in pazienti in età evolutiva con AIG e deficit posturali e di equilibrio: uno studio pilota |
Poster pubblicato in volume |
Go to |
2017 |
Terapia con Mecasermina in un bambino con iperinsulinismo congenito da mutazione INS-R |
Poster pubblicato in volume |
Go to |
2017 |
Effects of physical activity on postural balance in children with juvenile idiopathic arthritis: results from pilot study |
eedings |
Go to |
2017 |
VDR MUTATION IN TWO SISTERS: PHENOTYPE VARIABILITY AND CLINICAL OUTCOME |
Poster pubblicato in rivista |
Go to |
2017 |
GH TREATMENT ADHERENCE IN CHILDHOOD AND ADOLESCENCE IMPROVES USING EASYPODTM DEVICE: DATA DEMONSTRATION IN AN ITALIAN CENTRE |
Poster pubblicato in rivista |
Go to |
2017 |
MECASERMIN TREATMENT OF A CHILD WITH CONGENITAL HYPERINSULINISM LINKED TO INS-R MUTATION |
Poster pubblicato in rivista |
Go to |
2017 |
TERAPIA CON MECASERMINA IN UN BAMBINO CON IPERINSULINISMO CONGENITO DA MUTAZIONE DI INS-R |
Poster pubblicato in volume |
Go to |
2017 |
VALUTAZIONE CON EASYPODTM DELL’ADERENZA ALLA TERAPIA CON GH IN ETÀ PEDIATRICA E ADOLESCENZIALE: DATI DI UN CENTRO ITALIANO |
Poster pubblicato in volume |
Go to |
2017 |
RACHITISMO VITAMINA-D RESISTENTE DA MUTAZIONE DEL RECETTORE DELLA VITAMINA D: VARIABILITÀ FENOTIPICA IN DUE SORELLE |
Poster pubblicato in volume |
Go to |
2017 |
Genetic and clinical profile of a sicilian population with R92Q mutation |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2017 |
New diagnostic criteria of acute rheumatic fever: prevalence of silent carditis in a pediatric population |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2017 |
Hypocomplementemia in children with juvenile idiopatic arthritis treated with tocilizumab: personal records |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2017 |
Platelet count and MPV as predictive markers of atherosclerosis in familial Mediterranean fever |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2017 |
Pyridoxine dependent epilepsies: new therapeutical point of view. |
Lettera |
Go to |
2017 |
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment. |
Articolo in rivista |
Go to |
2017 |
Anti-IL1 in patients with low penetrance mutations for autoinflammatory diseases: tuscany and sicilian case series from paediatric to adult age |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2017 |
Genetic and clinical profile of a paediatric population with FMF in Sicily |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2017 |
Internet Addiction: Starting the Debate on Health and Well-Being of Children Overexposed to Digital Media. |
Articolo in rivista |
Go to |
2017 |
Preventive Effect of Cow's Milk Fermented with Lactobacillus paracasei CBA L74 on Common Infectious Diseases in Children: A Multicenter Randomized Controlled Trial. |
Articolo in rivista |
Go to |
2017 |
Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant. |
Articolo in rivista |
Go to |
2017 |
Epidemiology and diagnostic and therapeutic management of febrile seizures in the Italian pediatric emergency departments: A prospective observational study. |
Articolo in rivista |
Go to |
2017 |
Effects of Infant Formula With Human Milk Oligosaccharides on Growth and Morbidity: A Randomized Multicenter Trial. |
Articolo in rivista |
Go to |
2017 |
Caring for Infants and Children Following Alternative Dietary Patterns |
Articolo in rivista |
Go to |
2017 |
Dall'aderenza all'efficacia della terapia con GH: monitoraggio con device elettronico |
Abstract in atti di convegno pubblicato in volume |
Go to |
2016 |
Communication about vaccination: A shared responsibility |
Articolo in rivista |
Go to |
2016 |
Foster Care: A Fragile Reality Needing Social Attention, and Economic Investments. |
Articolo in rivista |
Go to |
2016 |
SINDROME DI PALLISTER KILLIAN. DESCRIZIONE DI UN CASO E CORRELAZIONE CLINICO GENETICA |
eedings |
Go to |
2016 |
Congenital heart defects in newborns with apparently isolated single gastrointestinal malformation: A retrospective study |
Articolo in rivista |
Go to |
2016 |
Early intestinal perforation secondary to congenital mesenteric defects |
Articolo in rivista |
Go to |
2016 |
Sindrome da microduplicazione 17p13.3: caratterizzazione di una nuova regione critica per la variante clinica con palatoschisi |
eedings |
Go to |
2016 |
Nuova mutazione del gene NIPBL in paziente affetto da Sindrome di Cornelia de Lange: report clinico e correlazione genotipo-fenotipo |
eedings |
Go to |
2016 |
Sindrome da duplicazione 1q21: variabile penetranza ed espressività clinica intrafamiliare di un riarrangimento genomico di circa 6 Mb non precedentemente descritto |
eedings |
Go to |
2016 |
INTELLECTUAL DISABILITY, EPILEPSY AND MILD DYSMORPHISMS DUE 22q11.2 DISTAL DUPLICATION: CLINICAL AND MOLECULAR CHARACTERIZATION OF A 0.5 Mb MINIMAL CRITICAL REGION |
Poster pubblicato in rivista |
Go to |
2016 |
PREVENTION OF NOSOCOMIAL INFECTIONS AND SURVEILLANCE OF EMERGING RESISTANCES IN A NEONATAL INTENSIVE CARE UNIT (NICU): A SIX-YEAR PROSPECTIVE COHORT STUDY |
eedings |
Go to |
2016 |
Precise reply and clarifications on behalf of Sicilian Public Health Authorities to the case report published by La Rosa and collegues |
Articolo in rivista |
Go to |
2016 |
Kawasaki disease in Sicily: clinical description and markers of disease severity |
Articolo in rivista |
Go to |
2016 |
Congenital cytomegalovirus related intestinal malrotation: a case report |
Articolo in rivista |
Go to |
2016 |
DISFUNZIONE MULTIORGANO (MOF) IN CORSO DI ENCEFALOPATIA NEONATALE. INDAGINE EPIDEMIOLOGICA SU UN CAMPIONE DI NEONATI OSSERVATI NEL PERIODO GENNAIO 2009 - MAGGIO 2016 |
Abstract non pubblicato |
Go to |
2016 |
Total Hemi-overgrowth in Pigmentary Mosaicism of the (Hypomelanosis of) Ito Type: Eight Case Reports. |
Articolo in rivista |
Go to |
2016 |
The power of stories in Pediatrics and Genetics |
Articolo in rivista |
Go to |
2016 |
Congenital muscular dystrophy: from muscle to brain. |
Review essay (rassegna critica) |
Go to |
2016 |
The "Invisible Children": Uncertain Future of Unaccompanied Minor Migrants in Europe. |
Articolo in rivista |
Go to |
2016 |
A Rare Case of Deletion in 2q24.1: Clinical Features and Response to Gh Hormone Treatment |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2016 |
Rickets as Precocious Sign of Celiac Disease |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2016 |
The Child Health Care System in Italy. |
Articolo in rivista |
Go to |
2016 |
Maternal Diet and Nutrient Requirements in Pregnancy and Breastfeeding. An Italian Consensus Document. |
Review essay (rassegna critica) |
Go to |
2016 |
The Role of Pediatricians in Caring for the Well-Being of Children Living in New Types of Families |
Articolo in rivista |
Go to |
2016 |
Impact of Distressing Media Imagery on Children |
Articolo in rivista |
Go to |
2016 |
Portal Vein Thrombosis in a Preterm Newborn with Mutation of the MTHFR and PAI-1 Genes and Sepsis by Candida parapsilosis |
Articolo in rivista |
Go to |
2015 |
Management of multiple pregnancy with an affected twin |
Articolo in rivista |
Go to |
2015 |
Parenting Stress Profile and Children Behaviour in Patients with Congenital Hypothyroidism |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2015 |
TUBEROUS SCLEROSIS COMPLEX IN A PATIENT CARRYING AN ATYPICAL GENOMIC REARRANGEMENT |
eedings |
Go to |
2015 |
Intellectual disabilitiy in developmental age |
Articolo in rivista |
Go to |
2015 |
Diagnosi precoce di disabilità intellettiva sindromica |
eedings |
Go to |
2015 |
Disabilità Intellettiva, riarrangiamenti genomici, ittioli |
eedings |
Go to |
2015 |
Antimicrobial therapy in neonatal intensive care unit |
Articolo in rivista |
Go to |
2015 |
Atresia digiuno-ileale tipo apple-peel: raro esordio neonatale di fibrosi cistica |
eedings |
Go to |
2015 |
The Burden of Respiratory Syncytial Virus Disease in Pre-Term Infants |
Articolo in rivista |
Go to |
2015 |
Methicillin-resistant Staphylococcus aureus nasal colonization in a level III neonatal intensive care unit: Incidence and risk factors |
Articolo in rivista |
Go to |
2015 |
The care pathway for children with urticaria, angioedema, mastocytosis |
Articolo in rivista |
Go to |
2015 |
Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients |
Articolo in rivista |
Go to |
2015 |
FOLLOW-UP DI SVILUPPO NEUROPSICOMOTORIO E CORRELAZIONI CON IL PONDERAL INDEX IN UN CAMPIONE DI NEONATI LATE PRETERM |
eedings |
Go to |
2015 |
Position Statement on Breastfeeding from the Italian Pediatric Societies |
Articolo in rivista |
Go to |
2015 |
QUELLE STRANE CHIAZZE.... |
Articolo in rivista |
Go to |
2015 |
4p16.1-p15.31 duplication and 4p terminal deletion in a 3-years old Chinese girl: Array-CGH, genotype-phenotype and neurological characterization |
Articolo in rivista |
Go to |
2015 |
Femicide and murdered women's children: Which future for these children orphans of a living parent? |
Articolo in rivista |
Go to |
2015 |
The Economic Burden of Child Maltreatment in High Income Countries |
Articolo in rivista |
Go to |
2015 |
Oxidative stress markers at birth: Analyses of a neonatal population |
Articolo in rivista |
Go to |
2015 |
Role of poultry meat in a balanced diet aimed at maintaining health and wellbeing: an Italian consensus document |
Articolo in rivista |
Go to |
2015 |
DYKE DAVIDOFF MASSON SYNDROME:PROFILO DI SVILUPPO NEURO-COGNITIVO A 4 ANNI IN UN PAZIENTE CON DIAGNOSI IN EPOCA NEONATALE |
eedings |
Go to |
2015 |
Radiation risks knowledge in resident and fellow in paediatrics: A questionnaire survey |
Articolo in rivista |
Go to |
2015 |
ERNIA DIAFRAMMATICA CONGENITA: COMPROMISSIONE TORACO-POLMONARE E DIAGNOSI GENETICA |
Articolo in rivista |
Go to |
2015 |
Dottore, mio figlio non impara a leggere”. I Disturbi Specifici dell’Apprendimento (DSA) e il pediatra di famiglia |
Articolo in rivista |
Go to |
2015 |
Survey of Italian pediatricians' perspectives and knowledge about neonatal screening |
Articolo in rivista |
Go to |
2015 |
Congenital generalized hypertrichosis: The skin as a clue to complex malformation syndromes |
Articolo in rivista |
Go to |
2015 |
Colonizzazione da Staphylococcus Aureus Meticillino-Resistente (MRSA) in epoca di vita neonatale nell’U.O. Neonatologia e TIN dell’AOUP “P.Giaccone” di Palermo nel periodo 2009 - 2015 |
eedings |
Go to |
2015 |
Prognostic Challenges of SCN1A Genetic Mutations: Report on Two Children with Mild Features |
Articolo in rivista |
Go to |
2015 |
School bullying: an international public health emergency correlated to psychosomatic problem as long-term sequelae |
Articolo in rivista |
Go to |
2015 |
ASFISSIA PERINATALE:VALUTAZIONE CLINICO-EPIDEMIOLOGICA IN UN CAMPIONE DI NEONATI DI ≥ 34 SEG |
Abstract in atti di convegno pubblicato in volume |
Go to |
2015 |
Functional gastrointestinal disorders: Dynamic observation of pediatric cases |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2015 |
Paternal uniparental disomy chromosome 14-like syndrome due a maternal de novo 160kb deletion at the 14q32.2 region not encompassing the IG- and the MEG3-DMRs: Patient report and genotype-phenotype correlation |
Articolo in rivista |
Go to |
2015 |
Sorveglianza dello sviluppo in soggetti con anomalie del setto pellucido. descrizione di un caso con agenzia isolata. |
eedings |
Go to |
2015 |
Prenatal tobacco smoke exposure increases hospitalizations for bronchiolitis in infants |
Articolo in rivista |
Go to |
2015 |
Risk factors for bronchiolitis hospitalization during the first year of life in a multicenter Italian birth cohort |
Articolo in rivista |
Go to |
2015 |
BRAINSTEM AUDITORY EVOKED POTENTIALS AND VISUAL POTENTIALS IN KAWASAKI DISEASE: EXPRESSION OF CNS VASCULITIS? |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2015 |
RHEUMATHOLOGIC DISEASES IN ADOLESCENCE: PSYCHOLOGICAL PROFILE OF A DIFFICULT AGE |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2015 |
Homozygosity for a Mutation in the CYP11B2 Gene and GH Deficiency in a Child with Severe Growth Delay |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2015 |
WIDENING THE SCOPE OF THE 15q13.3 MICRODUPLICATION SYNDROME. PATIENT REPORT AND GENOTYPE-PHENOTYPE CORRELATION. |
eedings |
Go to |
2014 |
Epilessia temporale e manifestazioni parossistiche neurovegetative in età prescolare: descrizione di un caso clinico emblematico |
eedings |
Go to |
2014 |
Deficit di GH e scarso accrescimento in fibrosi cistica: associazione casuale o causale ? |
eedings |
Go to |
2014 |
Grave ipotonia neonatale con artrogriposi: descrizione di un caso clinico e problematiche diagnostiche |
eedings |
Go to |
2014 |
Perinatal management of gastroschisis |
Articolo in rivista |
Go to |
2014 |
Unusual paroxysmal autonomic manifestations in a 22 month old girl |
eedings |
Go to |
2014 |
[The 2014 lifetime immunization schedule approved by the Italian scientific societies. Italian Society of Hygiene, Preventive Medicine, and Public Health. Italian Society of Pediatrics. Italian Federation of Pediatric Physicians. Italian Federation of General Medical Physicians. Arezzo Service of Legal Medicine] |
Articolo in rivista |
Go to |
2014 |
Adolescents with Chronic Endocrine Diseases:a Multidisciplinary Approach: the Experience of the Paediatric Clinic of Palermo |
eedings |
Go to |
2014 |
Auxological Pattern, BMI and Endocrine Follow Up in Children with Congenital Hypothiroidism: the Data of thePediatric Clinic of Palermo |
eedings |
Go to |
2014 |
Green nail syndrome |
Articolo in rivista |
Go to |
2014 |
Urinary 1H-NMR and GC-MS metabolomics predicts early and late onset neonatal sepsis |
Articolo in rivista |
Go to |
2014 |
Non c'é due senza tre: una sindrome autoinfiammatoria "complessa" |
eedings |
Go to |
2014 |
Intestinal tuberculosis in a child living in a country with a low incidence of tuberculosis: a case report |
Articolo in rivista |
Go to |
2014 |
Empirical examination of the indicator's pediatric gastroenteritis hospitalization rate based on administrative hospital data in Italy |
Articolo in rivista |
Go to |
2014 |
Inter-society consensus document on treatment and prevention of bronchiolitis in newborns and infants |
Articolo in rivista |
Go to |
2014 |
Bmi and Auxological Follow Up in Children with Hashimoto Thyroiditis: Utility of a Phisical Activity Program |
eedings |
Go to |
2014 |
Epidemiology of Toxoplasma and CMV serology and of GBS colonization in pregnancy and neonatal outcome in a Sicilian population |
Articolo in rivista |
Go to |
2014 |
Peritonite meconiale in una rara associazione
di atresia ileale apple-peel con difetto
di parete addominale |
Articolo in rivista |
Go to |
2014 |
Risk factors for refractory Kawasaki disease: clinical records of the paediatric clinic of palermo |
eedings |
Go to |
2014 |
Le infezioni nosocomiali |
Articolo in rivista |
Go to |
2014 |
New diagnostic possibilities in systemic neonatal infections: metabolomics |
Articolo in rivista |
Go to |
2014 |
Association of Maternal Hypertension and Chorioamnionitis With Preterm Outcomes |
Articolo in rivista |
Go to |
2014 |
Intrauterine growth pattern and birthweight discordance in twin pregnancies: a retrospective study |
Articolo in rivista |
Go to |
2014 |
Follow up auxologico, BMI ed assetto endocrino in bambini con ipotiroidismo congenito: esperienza della clinica pediatrica di Palermo |
eedings |
Go to |
2014 |
IL volume piastrinico medio nei pazienti con febbre mediterranea familiare in età pediatrica |
eedings |
Go to |
2014 |
Gestione pre eperinatale della malformazione adenoido-cistica polmonare congenita |
eedings |
Go to |
2014 |
La porpora di Seidlmayer: descrizione di cinque casi |
eedings |
Go to |
2014 |
Urinary metabolomics of bronchopulmonary dysplasia (BPD): preliminary data at birth suggest it is a congenital disease |
Articolo in rivista |
Go to |
2014 |
Il trattamento dell’insonnia in eta’ evolutiva: report clinico e revisione della letteratura |
Articolo in rivista |
Go to |
2014 |
Adiponectin, resistin and leptin in paediatric chronic renal failure: Correlation with auxological and endocrine profiles |
Articolo in rivista |
Go to |
2014 |
Trouble always comes in threes: three mutations for three auto inflammatory genes in a child and in his father |
eedings |
Go to |
2014 |
Clinical features and follow-up in patients with 22q11.2 deletion syndrome |
Articolo in rivista |
Go to |
2014 |
Una gonartrite postinfettiva: tre virus....un'articolazione |
eedings |
Go to |
2014 |
Monitoring neonatal fungal infection with metabolomics |
Articolo in rivista |
Go to |
2014 |
Effetti dell'obesità sulla funzionalità respiratoria in età pediatrica e fattori di rischio associati |
eedings |
Go to |
2014 |
RELATIONSHIP BETWEEN SECOND HAND SMOKE (SHS) EXPOSURE AND ATOPY IN SOCIAL DISADVANTAGED ASTHMATIC CHILDREN |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2014 |
Malattia di Kawasaki: un caso veramente "atipico" |
eedings |
Go to |
2014 |
Congenital Hyperinsulinism Linked to INS-R Mutation: Case Report |
eedings |
Go to |
2014 |
Le insidie dell'orticaria cronica: dall'iter diagnostico condiviso alle strategie terapeutiche |
eedings |
Go to |
2014 |
GENDER DIFFERENCES IN RHINITIC CHILDREN |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2014 |
Addison Disease and Atrophic Gastritis: High Persistent ACTH Levels Although an Adequate Treatment |
eedings |
Go to |
2014 |
Iperinsulinismo congenito da mutazione in omozigosi di INS-R: descrizione di un caso |
eedings |
Go to |
2014 |
"Un mare di bambini": progetto pilota condiviso LNI-SIP |
eedings |
Go to |
2014 |
Aspetti endocrini e profilo auxologico in bambini e adolescenti con fibrosi cistica |
Articolo in rivista |
Go to |
2014 |
New application of heart rate variability in newborns at developmental risk |
eedings |
Go to |
2014 |
Smoke exposure as a risk factor for asthma in childhood: A review of current evidence |
Articolo in rivista |
Go to |
2014 |
Variable phenotype in 17q12 microdeletions: Clinical and molecular
characterization of a new case |
Articolo in rivista |
Go to |
2014 |
Il sostegno multidisciplinare dell'adolescente con patologia reumatologica: progetto pilota della Clinica Pediatrica di Palermo |
eedings |
Go to |
2014 |
Effetti a breve termine del Diabate Mellito Materno sulla maturazione ossea |
eedings |
Go to |
2014 |
Predictive Factors of Abdominal Compartment Syndrome in Neonatal Age |
Articolo in rivista |
Go to |
2014 |
Il trattamento dei disturbi da comportamento dirompente in età evolutiva |
Articolo in rivista |
Go to |
2014 |
Response to Stanich et al.: Correspondence regarding-PTEN hamartoma tumor syndromes in childhood-Description of two cases and a proposal for follow-up protocol |
Articolo in rivista |
Go to |
2014 |
Meconial peritonitis in a rare association of partial ileal apple-peel atresia with small abdominal wall defect |
Articolo in rivista |
Go to |
2014 |
An unusual oral swelling |
Nota a sentenza |
Go to |
2014 |
Empirical validation of the "Pediatric asthma Hospitalization rate" indicator |
Articolo in rivista |
Go to |
2014 |
LA SEDAZIONE PROCEDURALE IN ONCOEMATOLOGIA PEDIATRICA |
Articolo in rivista |
Go to |
2014 |
Idiopathic Seidlmayer's Purpura: A Case Report |
Articolo in rivista |
Go to |
2014 |
PO-0994 Ltri in Paediatrics: Analysis Of An Annual Survey |
eedings |
Go to |
2014 |
Methicillin-resistant Staphylococcus aureus colonization: a three-year prospective study in a neonatal intensive care unit in Italy. |
Articolo in rivista |
Go to |
2014 |
Metabolomics in the diagnosis of sepsis |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2014 |
Seidlmayer’s purpura: five cases and review of the literature |
eedings |
Go to |
2014 |
Sindrome di S.A.P.H.O. e acne fulminans: storia di una rara associazione |
eedings |
Go to |
2013 |
THE EFFECTS OF PHYSICAL FITNESS ON CHILDREN WITH PREVIOUS NEOPLASIA |
eedings |
Go to |
2013 |
Second hand smoke (SHS) exposure in asthmatic children is associated with social disadvantage and atopy |
Abstract in atti di convegno pubblicato in rivista |
Go to |
2013 |
ASSOCIATION BETWEEN CELIAC DISEASE AND ENDOCRINE AUTOIMMUNE PATHOLOGIES |
eedings |
Go to |
2013 |
Twins among history, mith and arts |
Articolo in rivista |
Go to |
2013 |
TYPE AND COUNTER-TYPE FROM SPECIFIC CHROMOSOMAL REGIONS |
Articolo in rivista |
Go to |
2013 |
Outcome neonatale in stati di ipovitaminosiD |
eedings |
Go to |
2013 |
Il “late preterm”: un neonato pretermine attempato |
Articolo in rivista |
Go to |
2013 |
Third-hand smoke exposure and health hazards in children |
Articolo in rivista |
Go to |
2013 |
An acute headache due a nodulary swell- ing of the skull |
Abstract in rivista |
Go to |
2013 |
Newborn screening of inherited metabolic disorders by tandem mass spectrometry: past, present and future |
Articolo in rivista |
Go to |
2013 |
PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocol |
Articolo in rivista |
Go to |
2013 |
CUTANEOUS MANIFESTATIONS IN PEDIATRIC COELIAC DISEASE |
eedings |
Go to |
2013 |
Neonatal osteomyelitis of the talus due to methicillin-resistant Staphylococcus epidermidis |
Articolo in rivista |
Go to |
2013 |
Intrauterine growth restriction and congenital malformations: a retrospective epidemiological study |
Articolo in rivista |
Go to |
2013 |
Circolazione di MRSA in età pediatrica in ambiente ospedaliero e in comunità |
eedings |
Go to |
2013 |
Gemellarità e prematurità |
Capitolo o Saggio |
Go to |
2013 |
MYCOPLASMA PNEUMONIAE INFECTIONS IN PAEDIATRIC AGE: CLINICAL VARIABILITY |
eedings |
Go to |
2013 |
CONGENITAL DIAPHRAGMATIC HERNIA AND ESOPHAGEAL ATRESIA: THE IMPORTANCE OF RESPIRATORY FOLLOW-UP IN CONGENITAL THORACIC MALFORMATION |
Articolo in rivista |
Go to |
2013 |
THE VALUE OF FENO MEASUREMENT IN CHILDHOOD ASTHMA: UNCERTAINTIES AND PERSPECTIVES |
Articolo in rivista |
Go to |
2013 |
Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype? |
Articolo in rivista |
Go to |
2013 |
Delineating a new critical region for juvenile myoclonic epilepsy at the 22q11.2 chromosome |
Articolo in rivista |
Go to |
2013 |
Outbreak of colonizations by extended-spectrum β-lactamase-producing Escherichia coli sequence type 131 in a neonatal intensive care unit, Italy. |
Articolo in rivista |
Go to |
2013 |
Dyke-Davidoff-Masson syndrome: case report of fetal unilateral ventriculomegaly and hypoplastic left middle cerebral artery |
Articolo in rivista |
Go to |
2013 |
16P11.2 MICRODELETION/MICRODUPLICATION SYNDROME: FURTHER CHARACTERIZATION
OF A CRITICAL REGION FOR NEUROPSYCHIATRIC DEVELOPMENT |
Articolo in rivista |
Go to |
2013 |
MICROCEPHALY A CLINICAL-GENETIC AND NEUROLOGIC APPROACH |
Articolo in rivista |
Go to |
2013 |
Successful control of an outbreak of colonization by Klebsiella pneumoniae carbapenemase-producing K. pneumoniae sequence type 258 in a neonatal intensive care unit, Italy |
Articolo in rivista |
Go to |
2013 |
MALFORMATIONS OF CENTRAL NERVOUS SYSTEM: GENERAL ISSUES |
Articolo in rivista |
Go to |
2013 |
X-linked intellectual disability |
Articolo in rivista |
Go to |
2013 |
COPY NUMBER VARIATIONS IN THE ETIOLOGY OF EPILEPSY |
Articolo in rivista |
Go to |
2013 |
Survey of neonatal respiratory care and surfactant administration in very preterm infants in the Italian Neonatal Network |
Articolo in rivista |
Go to |
2013 |
COPY NUMBER VARIATIONS IN THE ETIOLOGY OF AUTISM SPECTRUM DISORDERS |
Articolo in rivista |
Go to |
2012 |
Post-chemotherapy physical fitness level on children with diagnosis
of leukemia: results of a pilot study |
eedings |
Go to |
2012 |
Assessment of Cardiac funcionality in term newborns born to diabetic mothers |
eedings |
Go to |
2012 |
The “Honeymoon Phase” in Children with Type 1 Diabetes Mellitus (T1DM): Frequency, Duration and Predictive Factors at Onset. |
eedings |
Go to |
2012 |
Congenital malformations |
Articolo in rivista |
Go to |
2012 |
Esordio precoce di febbre mediterranea familiare in paziente con triplice mutazione |
eedings |
Go to |
2012 |
ASMA, ATTIVITA’ FISICA E INQUINAMENTO IN PEDIATRIA |
Capitolo o Saggio |
Go to |
2012 |
Il sistema di educazione continua in medicina [The system of continuous medical education] |
Articolo in rivista |
Go to |
2012 |
An unusual traumatic ulceration of the tongue |
Articolo in rivista |
Go to |
2012 |
Triplice mutazione del gene della febbre mediterranea familiare in paziente con malattia di Kawasaki ed infezione da EBV |
eedings |
Go to |
2012 |
Post-chemotherapy physical fitness level on children with diagnosis of leukemia: results of a pilot study |
Abstract in rivista |
Go to |
2012 |
L’ATTIVITA’ FISICA NEI BAMBINI CON PREGRESSA NEOPLASIA: PREVENZIONE DEL RISCHIO NEUROMUSCOLARE E MUSCOLO-SCHELETRICO |
eedings |
Go to |
2012 |
Interstitial deletion of chromosome 2p15-16.1: report of two patients and critical review of current genotype-phenotype correlation. |
Articolo in rivista |
Go to |
2012 |
Espressività clinica in soggetti con mutazioni della marenostrina "asintomatiche": descrizione di una casistica. |
eedings |
Go to |
2012 |
LA PRESA IN CARICO INTEGRATA DELL’ ADOLESCENTE CON PATOLOGIA CRONICA: PROGETTO PILOTA PER UN AMBULATORIO DI ADOLESCENTOLOGIA |
eedings |
Go to |
2012 |
MALATTIA DI KAWASAKI ED INFEZIONE DA EBV IN PAZIENTE CON TRIPLICE MUTAZIONE DEL GENE DELLA FEBBRE MEDITERRANEA FAMILIARE |
eedings |
Go to |
2012 |
Pelvic magnetic resonance imaging in Turner syndrome. |
Abstract in rivista |
Go to |
2012 |
LA RMN NEL FOLLOW UP DELLA FUNZIONALITA’ GONADICA NELLE ADOLESCENTI CON S. DI TURNER |
eedings |
Go to |
2012 |
Functional pain in hospitalised and school children |
Articolo in rivista |
Go to |
2012 |
Le adolescenti con coagulopatie congenite: dalla terapia con estroprogestinici al follow-up endocrino. |
eedings |
Go to |
2012 |
ADIPONECTIN, LEPTIN, RESISTIN LEVELS IN CYSTIC FIBROSIS ADOLESCENTS |
Articolo in rivista |
Go to |
2012 |
PROGETTO PILOTA PER LO SVOLGIMENTO DELL’ATTIVITA’ MOTORIA IN BAMBINI E ADOLESCENTI CON PREGRESSA NEOPLASIA |
eedings |
Go to |
2012 |
14q13.1-21.1 Deletion Encompassing the HPE8 Locus in an Adolescent With Intellectual Disability and Bilateral Microphthalmia, But Without Holoprosencephaly |
Articolo in rivista |
Go to |
2012 |
DIAGNOSI E PROGNOSI DELLA MALATTIA DI KAWASAKI FRA MARKERS EMATOCHIMICI E CLINICI |
eedings |
Go to |
2012 |
Survey of neonatal respiratory support use in very preterm infants in Italy |
Articolo in rivista |
Go to |
2012 |
Bovine Lactoferrin prevents invasive fungal infections in very low birth weight infants: a randomized controlled trials |
Articolo in rivista |
Go to |
2012 |
Precocious puberty in Costello syndrome: case report. |
Abstract in rivista |
Go to |
2012 |
Studio dei potenziali evocati uditivi e visivi nella malattia di Kawasaki: markers di vasculite e conferma diagnostica |
eedings |
Go to |
2012 |
Congenital Malformations and Syndromes: Early Diagnosis and Prognosis |
Capitolo o Saggio |
Go to |
2012 |
Definizione prognostica della malattia di Kawasaki: identificazione di markers ematochimici e clinici in una casistica personale |
eedings |
Go to |
2012 |
INFLIXIMAB THERAPY IN MANAGING PEDIATRIC IBD |
eedings |
Go to |
2012 |
Prematurity and twinning |
Articolo in rivista |
Go to |
2012 |
Characterization of a complex rearrangement involving chromosomes 1, 4 and 8 by FISH and array-CGH |
Articolo in rivista |
Go to |
2012 |
A new mutation in EDA gene in X-linked hypohidrotic ectodermal dysplasia associated with keratoconus. |
Articolo in rivista |
Go to |
2012 |
LE ALTERAZIONI DEI POTENZIALI EVOCATI NELLA MALATTIA DI KAWASAKI: SUPPORTO DIAGNOSTICO IN UN ITER DIFFICILE |
eedings |
Go to |
2012 |
ADOLESCENTI CON SINDROME DI TURNER E MENARCA SPONTANEO: CORRELAZIONE CON CARIOTIPO, PARAMETRI ORMONALI E IMAGING PELVICA |
eedings |
Go to |
2012 |
ENCEFALOPATIA NEONATALE. IL RUOLO DELLA INFEZIONE. ANALISI DI UN CAMPIONE DI 1107 NEONATI RICOVERATI IN UTIN E TERAPIA SEMINTENSIVA |
eedings |
Go to |
2012 |
Array CGH identifies a 823 kb Microduplication at 22q 11.22 encompassing the Rab36 gene in a Child with Autism Spectrum Disorder and Mild Dysmorphism |
eedings |
Go to |
2012 |
Epidemic spread of ST1-MRSA-IVa in a neonatal intensive care unit, Italy. |
Articolo in rivista |
Go to |
2012 |
Global (pharmacological and non pharmacological) prevention of RSV infection |
Capitolo o Saggio |
Go to |
2011 |
Awareness of radiation protection issue in paediatric trainees. A questionnaire study. |
eedings |
Go to |
2011 |
Array-CGH and clinical characterization in a patient with subtelomeric 6p deletion without ocular dysgenesis |
Articolo in rivista |
Go to |
2011 |
UTILITÀ DELLO SCREENING ECO-DOPPLER TIROIDEO NEL DIABETE MELLITO TIPO 1 |
eedings |
Go to |
2011 |
PUBERTA’ PRECOCE IN SINDROME DI COSTELLO: FOLLOW-UP DI UNA RARA ASSOCIAZIONE |
eedings |
Go to |
2011 |
EPATITE AUTOIMMUNE E COINFEZIONE DA HHV6: DESCRIZIONE DI UN CASO IN ETA’ PEDIATRICA |
eedings |
Go to |
2011 |
Stevens-Johnson syndrome and cholestatic hepatitis induced by acute Epstein-Barr virus infection |
Articolo in rivista |
Go to |
2011 |
PROFILO ENDOCRINO E DENSITA’ MINERALE OSSEA IN ADOLESCENTI CON COAGULOPATIE CONGENITE IN TERAPIA CON ESTROPROGESTINICI |
eedings |
Go to |
2011 |
L’ADOLESCENTE CON PATOLOGIA DELL’EMOSTASI E MENOMETRORRAGIA: DALLA PROFILASSI AL FOLLOW-UP ENDOCRINO |
eedings |
Go to |
2011 |
The multicenter Italian birth cohort study on incidence and determinants of lower respiratory tract infection hospitalization in infants at 33 weeks of gestation or more: preliminary results. |
Articolo in rivista |
Go to |
2011 |
Trappole nella diagnosi di APLV in età pediatrica. |
eedings |
Go to |
2011 |
Phenotypic analysis of individuals with Costello syndrome due to HRAS p.G13C |
Articolo in rivista |
Go to |
2011 |
SINDROME DA MICRODELEZIONE 17q21.31: DESCRIZIONE DI UN CASO CON ELEVATA ESPRESSIVITA' CLINICA |
eedings |
Go to |
2011 |
FOLLOW UP DI UN CASO DI SINDROME DI COSTELLO CON PUBERTA’ PRECOCE |
eedings |
Go to |
2011 |
A novel VIM-type metallo-beta-lactamase (VIM-14) in a Pseudomonas aeruginosa clinical isolate from a neonatal intensive care unit |
Articolo in rivista |
Go to |
2011 |
Obiettivi comuni per la pediatria |
Articolo in rivista |
Go to |
2011 |
Caratteristiche del neonato sano e adattamento alla vita extrauterina. Il pediatra-neonatologo in sala parto |
Capitolo o Saggio |
Go to |
2011 |
Concordant Intestinal Atresia in Two Pairs of Monozygotic Twins |
Articolo in rivista |
Go to |
2011 |
A large view of CYP21 locus among Sicilians and other Populations: identification of a novel CYP21A2 variant in Sicily. |
Articolo in rivista |
Go to |
2011 |
Nutrizione a tutto tondo |
Articolo in rivista |
Go to |
2011 |
Prevention of nosocomial infections and surveillance of emerging resistances in NICU |
Articolo in rivista |
Go to |
2011 |
A retrospective follow up study on maternal age and infant mortality in two Sicilian districts |
Articolo in rivista |
Go to |
2011 |
Il dosaggio del lattato in neonati con distensione addominale come fattore prognostico di sindrome da compartimento addominale |
eedings |
Go to |
2011 |
TIROIDITE AUTOIMMUNE IN FENILCHETONURIA: DESCRIZIONE DI UNA NUOVA ASSOCIAZIONE |
eedings |
Go to |
2011 |
NEUROFIBROMATOSI DI TIPO 1 ED IPOTIROIDISMO SUB-CLINICO DA TIROIDITE AUTOIMMUNE: DESCRIZIONE DI UN CASO IN ETA’ PEDIATRICA |
eedings |
Go to |
2011 |
CONTROLLO GLICOMETABOLICO E ABITUDINI ALIMENTARI IN
ADOLESCENTI CON DIABETE MELLITO TIPO 1 |
eedings |
Go to |
2011 |
GROWTH HORMONE TREATMENT IN A PATIENT WITH LANGER MESOMELIC DYSPLASIA |
Articolo in rivista |
Go to |
2011 |
Molecular and clinical characterization of a small duplication Xp in a human female with psychiatric disorders |
Articolo in rivista |
Go to |
2011 |
I POTENZIALI EVOCATI UDITIVI E VISIVI: MARKERS DI VASCULITE IN CORSO DI MALATTIA DI KAWASAKI |
eedings |
Go to |
2011 |
Autoimmune thyroiditis and phenilketonuria: a new association |
Articolo in rivista |
Go to |
2011 |
The First Case of Myoclonic Epilepsy in a Child With a De Novo 22q11.2 Microduplication |
Articolo in rivista |
Go to |
2011 |
TIROIDITE DI HASHIMOTO IN BAMBINI CON FENILCHETONURIA: ASSOCIAZIONE CASUALE O CAUSALE? |
eedings |
Go to |
2011 |
Reference values of blood cell counts in the first days of life |
Articolo in rivista |
Go to |
2011 |
Awarness of radiation protection issue in paediatric trainees. A questionnaire study. |
eedings |
Go to |
2011 |
Inhaled Surfactant in the treatment of accidental Talc Powder inhalation: a new case report |
Articolo in rivista |
Go to |
2011 |
MANIFESTAZIONI ADDOMINALI E GONADICHE NELLA PORPORA DI SCHÖNLEIN-HENOCH: ESTRAPOLAZIONE DALLA CASISTICA DELLA CLINICA PEDIATRICA DI PALERMO |
eedings |
Go to |
2011 |
Transient hepatic nodular lesions associated with patent ductus venosus in preterm infants. |
Articolo in rivista |
Go to |
2011 |
Il neonato in "cammino". Dalla Nipiologia e dalla Puericultura alla Neonatologia e alla Terapia Intensiva Neonatale |
Articolo in rivista |
Go to |
2011 |
Un figlio su misura |
Articolo in rivista |
Go to |
2011 |
ENDOCRINE PROFILE, BMD EVALUATION, ESTROPROGESTINIC TREATMENT IN THE FOLLOW UP OF GIRLS WITH CONGENITAL COAGULOPATHIES |
Articolo in rivista |
Go to |
2011 |
Correlazione tra valori di PCDAI e livelli di ASCA in un gruppo di pazienti pediatrici affetti da malattia di Crohn |
eedings |
Go to |
2011 |
IDENTIFICAZIONE DI MARKERS EMATOCHIMICI E CLINICI UTILI NELLA DEFINIZIONE PROGNOSTICA DELLA MALATTIA DI KAWASAKI: ANALISI DI UNA CASISTICA PERSONALE |
eedings |
Go to |
2011 |
DOWN REGULATION OF LYMPHOCYTES APOPTOSIS IN GIRLS WITH PRECOCIOUS PUBERTY |
Poster pubblicato in rivista |
Go to |
2011 |
INFEZIONE DA MICOPLASMA ED ANEMIA EMOLITICA: DA TRIGGER AD INDUTTORE DI AUTOIMMUNITA' |
eedings |
Go to |
2011 |
RUOLO DELLA RMN NELLO STUDIO DELL’ASSETTO OVARICO ED UTERINO IN ADOLESCENTI CON S. DI TURNER |
eedings |
Go to |
2011 |
HYPERINSULINEMIA AND INCREASED HOMA-IR IN PAEDIATRIC PATIENTS WITH MODERATE CHRONIC RENAL INSUFFICIENCY |
eedings |
Go to |
2010 |
ANGIOEDEMA EREDITARIO DA DEFICIT DI C1-INIBITORE: IDENTIFICAZIONE GENETICA PRECOCE IN UN NUCLEO FAMILIARE |
eedings |
Go to |
2010 |
Tante promesse... anche da noi |
Articolo in rivista |
Go to |
2010 |
DOUBLE BLIND PLACEBO CONTROLLED FOOD CHALLENGE
USEFUL TO DISCONFIRM OVER ESTIMATED DIAGNOSIS OF
CMPA IN CHILDREN |
eedings |
Go to |
2010 |
Array CGH defined interstitial deletion on chromosome 14: a new case |
Articolo in rivista |
Go to |
2010 |
Biochemical markers in Celiac disease |
Articolo in rivista |
Go to |
2010 |
STUDIO DELLA FUNZIONALITA’ TIROIDEA NELL’INSUFFICIENZA RENALE CRONICA LIEVE-MODERATA: CASISTICA PEDIATRICA |
eedings |
Go to |
2010 |
MRSA ST22-IVa (EMRSA-15 clone) in Palermo, Italy |
Articolo in rivista |
Go to |
2010 |
Array-CGH defined chromosome 1p duplication in a patient with autism spectrum disorder, mild mental deficiency, and minor dysmorphic features |
Articolo in rivista |
Go to |
2010 |
Salute e ambiente. Un nuovo impegno di coscienza |
Articolo in rivista |
Go to |
2010 |
Insulin resistance in paediatric patients with mild-moderate chronic renal insufficiency |
eedings |
Go to |
2010 |
INSULINORESISTENZA IN PAZIENTI CON INSUFFICIENZA RENALE CRONICA IN ETA’ PEDIATRICA |
eedings |
Go to |
2010 |
Deletion of NSD1 exon 14 in Sotos syndrome: first description. |
Articolo in rivista |
Go to |
2010 |
The world of twins: an update |
Articolo in rivista |
Go to |
2010 |
Infliximab administration effective in the treatment of refractory Kawasaki Disease |
Articolo in rivista |
Go to |
2010 |
Celiac Disease: a widespread emerging condition in mediterranean countries. |
Capitolo o Saggio |
Go to |
2010 |
Effetti dell'allattamento al seno e dell'epoca di introduzione del glutine sullo sviluppo della malattia celiaca |
eedings |
Go to |
2010 |
I gemelli. Un profilo di Medicina Perinatale e Pediatrica |
Monografia |
Go to |
2010 |
Prospettive in Pediatria: innovazione nella tradizione. L'integrazione delle conoscenza tra neonatololgia e chirugia neonatale |
Articolo in rivista |
Go to |
2010 |
Lissencephalic syndromes: brain and beyond |
Articolo in rivista |
Go to |
2010 |
Gestione clinica dei pazienti con trisomia a lunga sopravvivenza |
eedings |
Go to |
2010 |
LA MALATTIA DI KAWASAKI: LA CASISTICA DELLA CLINICA PEDIATRICA DI PALERMO |
eedings |
Go to |
2010 |
A novel L1CAM mutation in a fetus detected by prenatal diagnosis |
Articolo in rivista |
Go to |
2010 |
The aristaless (Arx) gene: one gene for many "interneuronopathies" |
Articolo in rivista |
Go to |
2010 |
Thyroid dysfunction in pediatric patients with mild-moderate chronic renal insufficiency |
eedings |
Go to |
2010 |
Efficacia di FK506 per uso topico e Infliximab nel trattamento del coinvolgimento cutaneo nelle malattie infiammatorie croniche intestinali. |
eedings |
Go to |
2010 |
UNA STRANA RECIDIVA DI “MALATTIA DI KAWASAKI" |
eedings |
Go to |
2010 |
INFLIXIMAB IN THE TREATMENT OF PEDIATRIC IBD: A SINGLE CENTRE EXPERIENCE |
eedings |
Go to |
2010 |
Auxological, metabolic and endocrine follow-up in patients treated with valproic acid |
eedings |
Go to |
2009 |
CANDIDA SEPTIC THROMBOSIS OF THE LEFT ATRIUM IN TWINS: REPORT OF TWO CASES |
eedings |
Go to |
2009 |
Esperienze regionali in neonatologia. Ultime novità in devolution: la Sicilia |
eedings |
Go to |
2009 |
Development of a new S/MAR containing Minicircle DNA vector: a new promise for Gene Therapy. |
eedings |
Go to |
2009 |
Corticosteroidi nella HSP: l’enigma continua… |
eedings |
Go to |
2009 |
UTILIZZO DI FONTI INFORMATIVE MULTIPLE E PUNTI DI CRITICITA’ PER INTERVENTI DI SANITA’ PUBBLICA IN TEMA DI MORTALITA’ INFANTILE. Un’esperienza condotta in SICILIA |
eedings |
Go to |
2009 |
Epidemiological assessment of Respiratory Syncytial Virus infection in hospitalized infants, during the season 2005-2006 in Palermo, Italy |
Articolo in rivista |
Go to |
2009 |
Sindrome CDG tipo I: un caso ad elevata espressività clinica |
eedings |
Go to |
2009 |
Sindrome di Noonan: esperienza personale su ventuno pazienti |
eedings |
Go to |
2009 |
FOLLOW-UP 2003-2008 DEI NATI VERY LOW BIRTH WEIGHT: ESITI NEUROLOGICI |
eedings |
Go to |
2009 |
Malattia polmonare cronica nei neonati VLBW: studio di una casistica 2005-2007 |
eedings |
Go to |
2009 |
RABDOMIOLISI IN CORSO DI INFEZIONE DA VIRUS PARAINFLUENZALE TRATTATA CON PARACETAMOLO |
eedings |
Go to |
2009 |
Duplication 12q21 in a patient with autistic disorder |
eedings |
Go to |
2009 |
Profilo auxologico, metabolico ed endocrino in pazienti epilettici in età evolutiva in terapia con acido valproico |
eedings |
Go to |
2009 |
UNA NUOVA MUTAZIONE DEL GENE CREBBP IN UN BAMBINO CON SINDROME DI RUBINSTEIN TAYBI |
eedings |
Go to |
2009 |
Genetica e infezioni neonatali |
Articolo in rivista |
Go to |
2009 |
ADOLESCENTE CON DATTILITE DELLE MANI DA INFEZIONE DA HELICOBACTER PYLORI |
eedings |
Go to |
2009 |
PROFILO ENDOCRINO, LIVELLI DI ADIPONECTINA, RESISTINA, LEPTINA IN PAZIENTI CON INSUFFICIENZA RENALE CRONICA IN ETA’ EVOLUTIVA |
eedings |
Go to |
2009 |
DOUBLE BLIND PLACEBO CONTROLLED FOOD CHALLENGE USEFUL
TO DISCONFIRM OVER ESTIMATED DIAGNOSIS OF CMPA IN
CHILDREN |
eedings |
Go to |
2009 |
TROMBOSI VENOSA PROFONDA DA ESTROPROGESTINICI IN TETRASOMIA X |
eedings |
Go to |
2009 |
TRATTAMENTO CON INFLIXIMAB IN UN LATTANTE CON MALATTIA DI KAWASAKI RESISTENTE ALLE TERAPIE CONVENZIONALI |
eedings |
Go to |
2009 |
Infliximab and emerging biological treatment for pediatric Crohn’s disease. |
Articolo in rivista |
Go to |
2009 |
TIROIDITE AUTOIMMUNE IN S. DI LOWE: SEGNALAZIONE DI UNA NUOVA ASSOCIAZIONE |
eedings |
Go to |
2009 |
Enhanced 17hydroxyprogesterone levels in children with multiple sclerosis receving glatiramer |
Abstract in rivista |
Go to |
2009 |
Vantaggi della RMN intestinale a doppio contrasto nel monitoraggio del Crohn Pediatrico Fistolizzante |
eedings |
Go to |
2009 |
MULTIPLE PREGNANCY NEWBORN BABIES |
eedings |
Go to |
2009 |
Incremento dei livelli di 17-idrossiprogesterone in pazienti con sclerosi multipla in età pediatrica |
eedings |
Go to |
2009 |
Duplicazione de novo 9p22.3 in diagnosi prenatale |
eedings |
Go to |
2009 |
Malattia di Kawasaki tipica resistente a immunoglobuline e steroidi: uso di Infliximab. |
eedings |
Go to |
2009 |
IL NEONATO VARIAMENTE GROSSO |
Articolo in rivista |
Go to |
2009 |
SPANX-B and SPANX-C (Xq27 region) gene dosage analysis in Down's syndrome subjects with undescended testes |
Articolo in rivista |
Go to |
2009 |
SINDROME DI APERT, SVILUPPO NEUROPSICOMOTORIO E FUNZIONE VISIVA: FATTORI DI RISCHIO PROGNOSTICO IN TRE PAZIENTI |
eedings |
Go to |
2009 |
Marker cromosomico soprannumerario invdup10)(q10q11.22) de novo in adulto con azoospermia |
eedings |
Go to |
2009 |
FOLLOW-UP AUXOLOGICO, METABOLICO ED ENDOCRINO IN PAZIENTI IN ETÀ EVOLUTIVA IN TRATTAMENTO CON ACIDO VALPROICO |
eedings |
Go to |
2009 |
Caratterizzazione citogenetica e clinica di un caso con der(22)(22qter-
>22p11.2::16p11.2->16pter)mat |
eedings |
Go to |
2009 |
TERAPIA CON SURFACTANTE PER VIA AEROSOLICA NELL’INALAZIONE DA BOROTALCO |
eedings |
Go to |
2009 |
DOLORE PSICOGENO IN BAMBINI E ADOLESCENTI A SCUOLA E IN OSPEDALE. DATI PRELIMINARI |
eedings |
Go to |
2009 |
PREVALENCE OH HYPOSPADIAS IN ITALY ACCORDING TO SEVERITY, GESTATIONAL AGE AND BIRTWEIGHT: AN EPIDEMIOLOGICAL STUDY |
Articolo in rivista |
Go to |
2009 |
OBESITA'. I FATTORI PRECOCI DI RISCHIO |
Articolo in rivista |
Go to |
2009 |
A premature infant with Costello syndrome due to a rare G13C HRAS mutation |
Articolo in rivista |
Go to |
2009 |
EDEMA EMORRAGICO ACUTO DEL LATTANTE: DESCRIZIONE DI UN CASO |
eedings |
Go to |
2009 |
Utilità del test di provocazione orale in doppio cieco nell'esclusione della diagnosi di APLV |
eedings |
Go to |
2009 |
Identificazione di due nuove mutazioni del gene NF1 in pazienti affetti da neurofibromatosi |
eedings |
Go to |
2009 |
Atresia esofagea: management intensivo neonatale |
eedings |
Go to |
2009 |
L’ADOLESCENTE CON IPOGONADISMO IPOGONADOTROPO: LA CENTRALITA’ DEL RUOLO DEL PEDIATRA |
eedings |
Go to |
2009 |
Infliximab and topical tacrolimus administration effective in the treatment of Pyoderma Gangrenosum. |
eedings |
Go to |
2009 |
Monosomia parziale 4p e trisomia parziale 22q: quadro elettroclinico |
Abstract in rivista |
Go to |
2009 |
POTENZIALI EVOCATI VISIVI (PEV) IN NEONATI DA GRAVIDANZA PLURIMA: RELAZIONE CON LA DISCORDANZA IN PESO (AGA VS SGA) |
eedings |
Go to |
2009 |
Generalized anasarca as way of presentation of severe protein losing enteropathy. |
eedings |
Go to |
2009 |
Sindrome di Feingold da delezione 2p24 |
eedings |
Go to |
2009 |
Adiponectin, resistin, leptin levels in paediatric patients with chronic renal insufficiency: relationships with clinical, auxological and endocrine profiles |
Abstract in rivista |
Go to |
2009 |
Rabdomiolisi in corso di infezione da virus parainfluenzale: descrizione di un caso in età pediatrica. |
eedings |
Go to |
2009 |
INFEZIONI DELLE VIE URINARIE |
Capitolo o Saggio |
Go to |
2009 |
IDENTIFICATION OF TWO NEW MUTATIONS IN TRPS 1 GENE LEADING TO THE THRICHO-RHINO-PHALANGEAL SYNDROME TYPE I AND III |
Articolo in rivista |
Go to |
2008 |
Resistin, adinonectin, leptin levels in adolescent with cystic fibrosis. |
Abstract in rivista |
Go to |
2008 |
Ruolo della lungodegenza come rischio di sepsi neonatali late onset: esperienza di un biennio in UTIN |
eedings |
Go to |
2008 |
Nosocomial colonization due to imipenem-resistant Pseudomonas aeruginosa epidemiologically linked to breast milk feeding in a neonatal intensive care unit. |
Articolo in rivista |
Go to |
2008 |
Lo scorbuto in età pediatrica: descrizione di due casi recenti |
eedings |
Go to |
2008 |
Neuropatia periferica in corso di infezione da Helicobacter pylori e Mycoplasma Pneumoniae. |
eedings |
Go to |
2008 |
Duodenal Giardiasis: a diagnosis we should not neglect |
eedings |
Go to |
2008 |
Il follow-up del neonato pretermine |
Capitolo o Saggio |
Go to |
2008 |
Potenziali Evocati Visivi precoci in tre soggetti con sindrome di Apert |
eedings |
Go to |
2008 |
Il neonato ipotonico |
Articolo in rivista |
Go to |
2008 |
Mycoplasma Pneumoniae e neuropatia periferica. |
eedings |
Go to |
2008 |
Amido di mais nel management della dumping syndrome: una lezione maturata dalla malattia di Von Gierke. |
eedings |
Go to |
2008 |
Compliance ed efficacia del Palivizumab a distanza. La nostra esperienza relativa al triennio 2002-2005. |
eedings |
Go to |
2008 |
Sex reversal from functional disomy of Xp: Prenatal and post-mortem findings. |
Articolo in rivista |
Go to |
2008 |
Respiratory syncyntial virus infection in a Sicilian pediatric population: risk factors, epidemiology, and severity |
Articolo in rivista |
Go to |
2008 |
Q289P mutation in the FGFR2 gene: first report in a patient with type 1 Pfeiffer
syndrome. |
Articolo in rivista |
Go to |
2008 |
10qter deletion: A new case |
Articolo in rivista |
Go to |
2008 |
Neonato con spettro facio-auricolo-vertebrale a piena espressività clinica e grave compromissione funzionale. |
eedings |
Go to |
2008 |
Il neonato con malformazioni congenite |
Articolo in rivista |
Go to |
2008 |
Sciwora con mioclono spinale.Descrizione di un caso in età adolescenziale |
eedings |
Go to |
2008 |
Infezione da EBV e malattia di Stevens-Johnson. |
eedings |
Go to |
2008 |
Trisomia parziale prossimale 1q in diagnosi prenatale |
eedings |
Go to |
2008 |
Sindrome di Sotos: descrizione di un caso da ampia delezione del gene NSD1 |
eedings |
Go to |
2008 |
Ernia diaframmatica congenita: analisi dei fattori prognostici in 27 pazienti (2000-2006). |
eedings |
Go to |
2008 |
The Italian longitudinal cohort of newborn twins: a research opportunity |
Abstract in rivista |
Go to |
2008 |
Milk intolerance: a big trouble for little patients. |
Articolo in rivista |
Go to |
2008 |
Quando pensare ad una sindrome genetica in un adolescente |
Articolo in rivista |
Go to |
2008 |
I nanismi come problema |
Articolo in rivista |
Go to |
2008 |
Mild twin–twin transfusion syndrome: Clinical report. |
Articolo in rivista |
Go to |
2008 |
Mycoplasma Pneumoniae: analisi di una casistica annuale. |
eedings |
Go to |
2008 |
Patologia cromosomica complessa: mosaicismo a tre linee cellulari
[(45,X/46,X,der (X)/46,X,der(X),t(X;12)] de novo in una paziente con
note dismorfiche |
eedings |
Go to |
2008 |
L'alimentazione del neonato oggi. |
Articolo in rivista |
Go to |
2008 |
Il dolore nell'ambulatorio del pediatra |
eedings |
Go to |
2008 |
I gemelli: eterogeneità clinica e approccio multidisciplinare [Twins: Clinical heterogeneity and multidisciplinary approach] |
Articolo in rivista |
Go to |
2008 |
Health of immigrant children: Congenital disease |
Articolo in rivista |
Go to |
2008 |
CD 95 and TRAIL induced lymphocytes apoptosis in girls with precocious puberty. |
Abstract in rivista |
Go to |
2008 |
Disostosi acrofacciale tipo Nager |
eedings |
Go to |
2008 |
La sindrome di Silver Russell: un caso da disomia uniparentale del cromosoma 7 |
eedings |
Go to |
2008 |
Un nuovo caso di microdelezione 15qter: valutazioni cliniche,
genetiche e molecolari |
eedings |
Go to |
2008 |
Un vettore NON-virale contenente un elemento S-MAR (Scafold/Matrix Attachment)consente un'espressione persistente nel tessuto epatico nel modello murino. |
eedings |
Go to |
2008 |
Idatidosi polmonare in età pediatrica: descrizione di un caso. |
eedings |
Go to |
2008 |
L'umanizzazione dell'assistenza in Terapia Intensiva Neonatale |
eedings |
Go to |
2008 |
Osteogenesi imperfetta e deficit di GH: descrizione di una rara associazione. |
eedings |
Go to |
2008 |
Sindrome di Smith Magenis da delezione 17
q 11.2: descrizione di un caso ad elevata espressività clinica |
eedings |
Go to |
2008 |
Duplicazione della regione critica per la sindrome di Down in un feto
con cardiopatia |
eedings |
Go to |
2008 |
The hairy elbows syndrome: clinical and neuroradiological findings. |
Articolo in rivista |
Go to |
2008 |
VRS: Applicazione di uno "score di rischio" italiano su data base nazionali. |
eedings |
Go to |
2008 |
Un caso di sindrome di Mauriac nel 2007 |
eedings |
Go to |
2008 |
Neonatal sepsis caused by Ralstonia pickettii |
Articolo in rivista |
Go to |
2007 |
Bronchiolitis: The new American Academy of Pediatrics Guidelines |
Articolo in rivista |
Go to |
2007 |
Preditttori fetali di aterosclerosi |
Articolo in rivista |
Go to |
2007 |
Epidemiologia dell'infezione da VRS a Palermo: 2 anni di esperienza |
eedings |
Go to |
2007 |
La sequenza di Pierre Robin: quando l’approccio conservativo fallisce |
eedings |
Go to |
2007 |
Epidemiologia della sordità geneticamente trasmessa nella popolazione siciliana |
eedings |
Go to |
2007 |
Malattia di Kawasaki: modalità di esordio e decorso clinico |
Articolo in rivista |
Go to |
2007 |
Sindrome di Pfeiffer: identificazione di una nuova mutazione nel gene FGFR2. |
Articolo in rivista |
Go to |
2007 |
IBD does not always travel alone. |
eedings |
Go to |
2007 |
Studio neurofisiologico dei potenziali evocati uditivi e visivi in bambini affetti da malattia di Kawasaki: contributo personale. |
eedings |
Go to |
2007 |
La vita prenatale, il parto e il neonato |
Capitolo o Saggio |
Go to |
2007 |
Patologia cromosomica rara: duplicazione 22qter |
eedings |
Go to |
2007 |
Serum Leptin Levels in young patients with beta-thalassemia major: personal records |
eedings |
Go to |
2007 |
Studio neurofisiologico dei potenziali evocati uditivi e visivi in bambini affetti da malattia di Kawasaki: contributo personale. |
Articolo in rivista |
Go to |
2007 |
ONLINE MENDELIAN INHERITANCE IN MAN (OMIM) |
Articolo in rivista |
Go to |
2007 |
Nutrizione del neonato pretermine: attualità e prospettive |
Articolo in rivista |
Go to |
2007 |
Ospedalizzazione da VRS: popolazione a rischio e curva epidemica in Sicilia |
eedings |
Go to |
2007 |
Aspetti di etica e management nelle UTIN ed intorno alla rianimazione neonatale |
eedings |
Go to |
2007 |
Storia e tradizioni su nascita e alimentazione del bambino in Sicilia |
Capitolo o Saggio |
Go to |
2007 |
PSEUDOIPOALDOSTERONISMO DI TIPO III IN NEONATO CON GRAVE REFLUSSO VESCICO‐URETERALE BILATERALE |
eedings |
Go to |
2007 |
Epidemiology of severe RSV infection in Palermo, a sicilian pediatric population: identifying risk factors, epidemic wave and severity |
eedings |
Go to |
2007 |
A case of Kawasaki disease mimicking acute appendicitis |
Articolo in rivista |
Go to |
2007 |
Cisti congenita del surrene ad esordio intrauterino: dalla diagnosi prenatale all'intervento precoce |
eedings |
Go to |
2007 |
Disturbo di regolazione in un campione a rischio: risultati di una intervista di screening ai genitori. |
Articolo in rivista |
Go to |
2007 |
Il bambino non è un adulto in miniatura |
Capitolo o Saggio |
Go to |
2007 |
Sindrome di Pfeiffer:identificazione di una nuova mutazione nel gene FGFR2 |
eedings |
Go to |
2007 |
SCLERODEMIA SISTEMICA: DESCRIZIONE DI UN CASO IN ETA’ PEDIATRICA |
eedings |
Go to |
2007 |
MALATTIA DI KAWASAKI: MODALITA’ DI ESORDIO E
DECORSO CLINICO |
eedings |
Go to |
2007 |
Disturbo di regolazione in un campione a rischio: risultati di una intervista di screening ai genitori |
eedings |
Go to |
2007 |
Le frontiere della neonatologia |
Capitolo o Saggio |
Go to |
2007 |
Fibrosi cistica e tolleranza glucidica: esperienza del Centro Regionale di Palermo |
eedings |
Go to |
2007 |
Sindrome di Down da duplicazione della regione critica 21q22.2-q22.3 |
eedings |
Go to |
2007 |
Oriental facial features, growth impairment, mental retardation, hypotonia, severe scoliosis, and precocious thelarche in females. |
Articolo in rivista |
Go to |
2007 |
Sorveglianza della mortalità infantile nella provincia di Palermo. Dati prelminari. |
Articolo in rivista |
Go to |
2007 |
Surveillance of multidrug-resistant gram-negative bacilli in a neonatal intensive
care unit: prominent role of cross transmission |
Articolo in rivista |
Go to |
2007 |
Unilateral multicystic dysplastic kidney in infants exposed to antiepileptic drugs during pregnancy |
Articolo in rivista |
Go to |
2007 |
Sindromi con macrosomia neonatale: esperienza clinica |
Articolo in rivista |
Go to |
2007 |
Pain in Paediatric Hospital Units |
Articolo in rivista |
Go to |
2007 |
Atresie del canale digerente nel neonato: esperienza di 4 anni |
eedings |
Go to |
2007 |
Il latante: le particolari attenzioni nel primo anno di vita |
Capitolo o Saggio |
Go to |
2007 |
Sclerodermia sistemica: descrizione di un caso in età pediatrica. |
Articolo in rivista |
Go to |
2007 |
Febbre mediterranea familiare: un caso atipico con esordio precoce. |
Articolo in rivista |
Go to |
2007 |
Sclerodermia sistemica: descrizione di un caso in età pediatrica |
eedings |
Go to |
2007 |
Un caso inusuale di malattia emolitica. |
eedings |
Go to |
2007 |
Il taglio cesareo tra urgenza ed elezione |
Articolo in rivista |
Go to |
2007 |
Screening ecografico cerebrale nel neonato sano:descrizione di 3 casi di cisti aracnoidea |
eedings |
Go to |
2007 |
Polycystic ovary and gonadoblastoma in Turner's syndrome. |
Articolo in rivista |
Go to |
2007 |
Sindrome di Turner in mosaico in madre e figlia con anomalie del cariotipo apparentemente non correlate. |
eedings |
Go to |
2007 |
Marker cromosomico soprannumerario inv/dup 15 ed autismo |
eedings |
Go to |
2007 |
Epidemiological study of nonsyndromic hearing loss in sicilian newborns |
Articolo in rivista |
Go to |
2007 |
Trisomia terziaria da segregazione 3:1, descrizione di due casi clinici |
Articolo in rivista |
Go to |
2007 |
Maxima debetur puero reverentia |
Articolo in rivista |
Go to |
2007 |
UNA STRANA FORMA DI PSEUDOCCLUSIONE INTESTINALE |
Articolo in rivista |
Go to |
2007 |
Displasia setto-ottica: descrizione di un caso con progressivo deterioramento dei PEV |
eedings |
Go to |
2007 |
Maxima debetur puro reverentia |
Capitolo o Saggio |
Go to |
2007 |
Gluten-Free Diet Impact on Leptin Levels in Asymptomatic Coeliac Adolescents: One Year of Follow-Up |
Articolo in rivista |
Go to |
2007 |
Ernia diaframmatica congenita. Analisi dei fattori prognostici in 27 pazienti (2000-2006) |
eedings |
Go to |
2007 |
Diagnosi genetica pre e post-natale: clinica ed etica |
eedings |
Go to |
2007 |
Hypogonadotropic hypogonadism in Kabuki syndrome: the story of two adolescents |
eedings |
Go to |
2007 |
Apoptosi linfocitaria CD95 e trail mediata in pazienti con pubertà precoce |
eedings |
Go to |
2007 |
Un caso inusuale di anemia emolitica |
Articolo in rivista |
Go to |
2007 |
Apolipoprotein E genotypic frequencies among Down syndrome patients imply early unsuccessful aging for ApoE4 carriers |
Articolo in rivista |
Go to |
2007 |
UN CASO INUSUALE DI ANEMIA EMOLITICA |
eedings |
Go to |
2006 |
IX SINDROME DI RETT DA AMPIA DELEZIONE DEL GENE MeCP2. |
eedings |
Go to |
2006 |
Sindrome di Rett da ampia delezione del gene MeCP2 |
eedings |
Go to |
2006 |
Associazione VACTERL incompleta: descrizione di 2 neonati senza atresia esofagea |
eedings |
Go to |
2006 |
PATTERN ENDOCRINO DELLA SINDROME DI WILLIAMS IN ETA’ EVOLUTIVA: CASISTICA PERSONALE |
eedings |
Go to |
2006 |
IPOGONADISMO IPOGONADOTROPO IN SINDROME DI KABUKI: DESCRIZIONE DI DUE CASI IN ETA’ EVOLUTIVA |
eedings |
Go to |
2006 |
Nutrizione e genetica |
Capitolo o Saggio |
Go to |
2006 |
MICROLITIASI TESTICOLARE BILATERALE IN SINDROME ADRENOGENITALE LATE ONSET |
eedings |
Go to |
2006 |
Duplicazione parziale Xq22.3-Xq25 in un soggetto di sesso femminile con anomalie fenotipiche |
eedings |
Go to |
2006 |
Il dolore da procedura in età neonatale |
Articolo in rivista |
Go to |
2006 |
VALUTAZIONE AUXOLOGICA ED ENDOCRINA NELLA S. DI AARSKORG: CASISTICA PEDIATRICA |
eedings |
Go to |
2006 |
Leri-Weill’s syndrome: clinical, radiological and genetic investigations in five patients |
Articolo in rivista |
Go to |
2006 |
Primary repair in esophageal atresia.The results of long term follow-up. |
Articolo in rivista |
Go to |
2006 |
Congenital rubella sindrome in an extremely low birth weight infant |
Articolo in rivista |
Go to |
2006 |
La sindrome di prader-Willi: una realtà nuova per una malattia già classica |
Articolo in rivista |
Go to |
2006 |
ADOLESCENTI IMMIGRATE E SINDROME DI TURNER: PROBLEMATICITA’ DI UN FOLLOW UP E DI UNA TERAPIA CRONICA IN DIFFERENTI ETNIE |
eedings |
Go to |
2006 |
Multiple food intolerance or refractory celiac sprue? |
Articolo in rivista |
Go to |
2006 |
Prevalenza delle mutazioni in GJB2 nella popolazione siciliana affetta da sordità neurosensoriale. |
eedings |
Go to |
2006 |
Non sempre la MICI viaggia da sola. |
eedings |
Go to |
2006 |
Il counselling genetico. |
Articolo in rivista |
Go to |
2006 |
Dolore da disturbi psichici nei bambini |
Articolo in rivista |
Go to |
2006 |
Artrogriposi multipla congenita da lesione del II motoneurone, descrizione di un caso e considerazioni clinico-diagnostiche. |
eedings |
Go to |
2006 |
Riarrangiamento cromosomico subtelomerico Del 10Q25: descrizione di un caso con elevata espressività clinica. |
eedings |
Go to |
2006 |
Quando la MICI va dal reumatologo |
eedings |
Go to |
2006 |
Sorveglianza della mortalità infantile nella Provincia di Palermo |
eedings |
Go to |
2006 |
SINDROME DA ASTINENZA NEONATALE |
eedings |
Go to |
2006 |
CISTI CONGENITA DELLA TESTA DEL PANCREAS: DALLA DIAGNOSI PRENATALE ALL’INTERVENTO PRECOCE |
eedings |
Go to |
2006 |
FOLLOW-UP AUXOLOGICO ED ENDOCRINO IN PAZIENTI CON SINDROME DI WILLIAMS IN ETA’ EVOLUTIVA |
eedings |
Go to |
2006 |
Mielodisplasia transitoria in un neonato con sindrome di Down |
eedings |
Go to |
2006 |
Caratteristiche epidemiologiche dell’Infezione da virus respiratorio sinciziale in Sicilia: dati preliminari su una casistica di infettivologia pediatrica |
eedings |
Go to |
2006 |
LEPTIN LEVELS IN ASYMPTOMATIC COELIAC ADOLESCENTS: ONE YEAR OF FOLLOW-UP IN GLUTEN-FREE DIET |
eedings |
Go to |
2006 |
Familial Protein Losing Enteropathy |
eedings |
Go to |
2006 |
Programmi di sorveglianza nosocomiale: esperienza di una UTIN; XXXV Congresso Regionale SIP, X Congresso Regionale SIN, III Congresso Regionale SIMEUP, Ragusa 16-18 novembre 2006. |
eedings |
Go to |
2006 |
La trombofilia ereditaria e le complicanze gravidiche nella popolazione siciliana. |
eedings |
Go to |
2006 |
ENDOCRINE, AUXOLOGICAL AND CLINICAL FOLLOW UP IN CONNATAL HIV-INFECTED CHILDREN: PERSONAL EXPERIENCE |
eedings |
Go to |
2006 |
Due casi di sclerosi tuberosa (o malattia di Bourneville) da mutazione del gene TSC2. |
eedings |
Go to |
2006 |
Endocrine, auxological and clinical follow up of connatally HIV-infected children: personal experience |
eedings |
Go to |
2006 |
Dieci anni di pediatria: che cosa è cambiato nella genetica |
Articolo in rivista |
Go to |
2006 |
ILDOLORE NELLA FIBROSI CISTICA |
eedings |
Go to |
2006 |
In puero homo: la vita prenatale, il parto e il neonato |
Articolo in rivista |
Go to |
2006 |
Displasia multicistica monolaterale in due neonati esposti in utero a farmaci antiepilettici |
eedings |
Go to |
2006 |
Una nuova mutazione nell’esone 4 del gene del FVIII causa un quadro di emofilia moderata. |
eedings |
Go to |
2006 |
Displasia setto-ottica,; descrizione di un caso ad esordio precoce. |
eedings |
Go to |
2006 |
Un problema tuttora aperto: update sulle infezioni respiratorie virali nei neonati a rischio. |
Articolo in rivista |
Go to |
2006 |
APPENDICITE ACUTA COME ESORDIO DI MALATTIA DI KAWASAKI: DESCRIZIONE DI UN CASO |
eedings |
Go to |
2006 |
Da uno a 14 anni e dai 15 a 19: fra gioco e scuola |
Articolo in rivista |
Go to |
2006 |
Maternal hyperphenylalaninemia syndrome: neuropsychological evaluation of four subjects during childhood and adolescence. |
Articolo in rivista |
Go to |
2006 |
Associazione CHARGE: descrizione di 2 casi con elevata espressività clinica. |
eedings |
Go to |
2006 |
IRSUTISMO SEVERO IN SINDROME DI KABUKI: DESCRIZIONE DI UN CASO |
eedings |
Go to |
2006 |
Integrated management of children with malformations: the example of Down's syndrome |
eedings |
Go to |
2006 |
Prevalenza delle mutazioni in GJB2 nella popolazione siciliana affetta da sordità neuro-sensoriale non sindromica |
eedings |
Go to |
2006 |
An interesting question of Pompe disease. A case report |
Articolo in rivista |
Go to |
2005 |
Rare chromosomal abnormalities: a mosaic of four cellular lines with two rings involving the chromosomes X and 21. First report in a male newborn patient |
Articolo in rivista |
Go to |
2005 |
La medicina preventiva, patrimonio culturale dei pediatri. I. Argomenti emergenti per il bambino, anzi, già per il neonato |
Articolo in rivista |
Go to |
2005 |
Surveillance of enteric virus infections in a neonatal intensive care unit. |
Articolo in rivista |
Go to |
2005 |
I nati da procreazione assistita – Rischio genetico e malformativo |
Articolo in rivista |
Go to |
2005 |
FOLLOW UP AUXOLOGICO IN UN BAMBINO CON FIBROSI CISTICA E DEFICIT DI GH |
eedings |
Go to |
2005 |
UN EDEMA MOLTO SOSPETTO IN UN NEONATO IPOTONICO |
Articolo in rivista |
Go to |
2005 |
Le cardiopatie congenite nella sindrome di Down: contributo clinico |
eedings |
Go to |
2005 |
Policistosi ovarica e gonadoblastoma in sindrome di Turner SRY positiva |
eedings |
Go to |
2005 |
DIABETE INSIPIDO E PANIPOPITUITARISMO IN IDROCEFALO CONGENITO: DESCRIZIONE DI UN CASO |
eedings |
Go to |
2005 |
Registro ISMAC Sicilia Occidentale - Attività 2000-2004 |
Monografia |
Go to |
2005 |
L'ipotonia congenita: cause genetiche |
Articolo in rivista |
Go to |
2005 |
Sindrome di Cornelia de Lange con deficit parziale di 21-Idrossilasi: segnalazione di una possibile associazione |
eedings |
Go to |
2005 |
“Aneurisma del setto interatriale associato a flutter atriale ad esordio prenatale”. |
eedings |
Go to |
2005 |
Perlman sindrome: Clinical report and nine-year follow-up |
Articolo in rivista |
Go to |
2005 |
I nati da procreazione assistita – Rischio perinatale |
Articolo in rivista |
Go to |
2005 |
Stipiti di Pseudomonas aeruginosa MBL produttori in Unità di Terapia Intensiva
Neonatale (UTIN) |
eedings |
Go to |
2005 |
Utilità degli ASCA nel follow up della malattia di Crohn. |
eedings |
Go to |
2005 |
Intolleranza al latte: nuovo algoritmo diagnostico. |
eedings |
Go to |
2005 |
Sindrome di Aicardi: correlati elettroclinici e follow-up in un caso con associate multiple anomalie cerebrali. |
eedings |
Go to |
2005 |
Complicanze endocrine nella talassemia: studio di 256 pazienti |
eedings |
Go to |
2005 |
Congenital hepatic mesenchymal hamartoma associated with mesenchymal stem villous hyperplasia of the placenta: case report |
Articolo in rivista |
Go to |
2005 |
Scuola e pediatria |
Articolo in rivista |
Go to |
2005 |
Evaluation of cytokine polymorphisms (TNFα, IFNγ and IL-10) in Down patients with celiac disease |
Articolo in rivista |
Go to |
2005 |
A single amino acid change A19V in perforin: a novel, frequent predisposing factor to childhood acute lymphoblastic leukemia? |
Articolo in rivista |
Go to |
2005 |
Il dolore nelle emopatie infantili. Dati preliminari. |
Articolo in rivista |
Go to |
2005 |
Microvillous Inclusion Disease in a newborn with positive family history of intractable diarrhoea |
Articolo in rivista |
Go to |
2005 |
Test genetici: ambiti di applicazione, limiti, prospettive. |
Articolo in rivista |
Go to |
2005 |
Le problematiche IUGR nei gemelli |
Articolo in rivista |
Go to |
2005 |
Displasia multicistica renale in rene ectopico: descrizione di un caso con anamnesi positiva per assunzione di farmaci antiepilettici della madre in gravidanza |
eedings |
Go to |
2005 |
Deficit di 17-alfa-idrossilasi: follow up sino alla statura definitiva |
eedings |
Go to |
2005 |
GENITALI PICCOLI |
Capitolo o Saggio |
Go to |
2005 |
IPOTIROIDISMO IN SINDROME DI CRIGLER-NAJJAR DI TIPO 2 ED ETEROZIGOSI PER SINDROME DI GILBERT: QUANDO L’ITTERO NON PUO’ REGREDIRE |
eedings |
Go to |
2005 |
Infliximab indispensabile per la remissione clinica nella malattia di Crohn refrattaria alla terapia tradizionale. |
eedings |
Go to |
2005 |
Ipotiroidismo e sindrome di Down: valutazione su 328 soggetti in età evolutiva |
eedings |
Go to |
2005 |
Trisomia da interscambio da traslocazione cromosomica reciproca bilanciata materna |
eedings |
Go to |
2005 |
Diabete insipido centrale da idrocefalo congenito in un neonato di genitori immigrati |
eedings |
Go to |
2005 |
Allattamento al seno: indagine conoscitiva SIP Sicilia. Risultati e commenti |
Articolo in rivista |
Go to |
2005 |
Il pediatra ed i nati da fecondazione artificiale |
eedings |
Go to |
2005 |
Ermafroditismo vero da traslocazione X;Y in un lattante |
eedings |
Go to |
2005 |
Il Problema del nato morto in Italia |
Articolo in rivista |
Go to |
2005 |
Malformazioni congenite nei neonati da genitori stranieri |
Capitolo o Saggio |
Go to |
2005 |
Sviluppo dell'apparato genitale maschile - Genitali piccoli |
Monografia |
Go to |
2005 |
Squilibrio elettrolitico e iperpigmentazione di cute e mucose: un'associazione temibile |
Articolo in rivista |
Go to |
2005 |
Sindrome di Turner 45,XO/46,XY: Una diagnosi citogenetica di rischio neoplastico |
eedings |
Go to |
2005 |
Atresia delle vie biliari in situs viscerum inversus, destrocardia ed idronefrosi: descrizione di un caso |
eedings |
Go to |
2005 |
Arteria ombelicale unica (AOU): un marker di anomalie congenite |
eedings |
Go to |
2005 |
Irsutismo in sindrome microcefalia con sinostosi radio-ulnare: prima segnalazione di una associazione |
eedings |
Go to |
2005 |
Aplasia surrenalica congenita X-Linked in una coppia di fratelli: follow up sino all'età puberale |
eedings |
Go to |
2005 |
Anastomosi primaria nell'atresia esofagea: risultati del follow-up |
eedings |
Go to |
2005 |
Epidemiologia Della Sordità Geneticamente Trasmessa Nella Popolazione Siciliana |
eedings |
Go to |
2005 |
Macrocefalia: analisi dei fattori predittivi di compromissione dello sviluppo neuropsicomotorio in un campione selezionato di 22 casi. |
eedings |
Go to |
2005 |
IL DOLORE NELLE EMOPATIE INFANTILI |
Articolo in rivista |
Go to |
2005 |
Patologia cromosomica rara:47,XXX / 48 XXXX. |
eedings |
Go to |
2005 |
Irsutismo in sindrome microcefalica e sinostosi radio-ulnare: prima segnalazione di una associazione |
eedings |
Go to |
2005 |
Ipotiroidismo in sindrome di Crigler-Najjar di tipo 2 ed eterozigoti per sindrome di Gilbert: quando l’ittero non può regredire. |
eedings |
Go to |
2005 |
Six patients with Pro250Arg mutation in FGFR3 in a family with coronal craniosynostosis: intrafamilial variability and clinical management |
Articolo in rivista |
Go to |
2005 |
DETECTION OF A NEW VIM TYPE METALLO-BETA-LACTAMASE (VIM 11) IN A PSEUDOMONAS AERUGINOSA CLINICAL ISOLATE FROM ITALY |
eedings |
Go to |
2005 |
3 nuovi pazienti con piccolo cromosoma soprannumerario derivato dal cromosoma 5 |
eedings |
Go to |
2005 |
Il Dolore nelle malattie infantili |
eedings |
Go to |
2005 |
Malformazione Adenomatoide Cistica del polmone (CAM): il neonato asintomatico |
eedings |
Go to |
2005 |
Dysmorphic face, precociously senile appearance, microcephaly, growth retardation and neuropsychomotor delay |
Articolo in rivista |
Go to |
2004 |
Obesità nella sindrome di Down: analisi di 320 soggetti in età evolutiva |
eedings |
Go to |
2004 |
ASPETTI PATOFISIOLOGICI DEL VIRUS RESPIRATORIO SNCIZIALE |
Articolo in rivista |
Go to |
2004 |
LONG GAP ESOPHAGEAL ATRESIA AND ASSOCIATED ANOMALIES ATRESIA ESOFAGEA “LONG GAP” ED ANOMALIE ASSOCIATE |
Articolo in rivista |
Go to |
2004 |
Osservazioni cliniche su due coppie di gemelli monozigotici discordanti per la presenza di anencefalia |
eedings |
Go to |
2004 |
17βhydroxysteroid deydrogenase-3 deficiency (17β HSD): clinical and endocrine features and molecular biology in two prepubertal patients |
Poster pubblicato in volume |
Go to |
2004 |
NEUROFIBROMATOSI E MALATTIE NEOPLASTICHE NELL’INFANZIA |
eedings |
Go to |
2004 |
La neurofibromatosi 1 in età evolutiva: contributo casistico e revisione clinica |
eedings |
Go to |
2004 |
LA NUTRIZIONE PARENTERALE E L’INTESTINO RESIDUO: QUALE RELAZIONE NEL DECORSO DI PAZIENTI CON SINDROME DA INTESTINO CORTO? VALUTAZIONE DA UNA CASISTICA NAZIONALE MULTICENTRICA |
Articolo in rivista |
Go to |
2004 |
Aneurisma del setto interatriale associato a flutter atriale ad esordio prenatale. |
Articolo in rivista |
Go to |
2004 |
Il neonato ipossico |
eedings |
Go to |
2004 |
Genetic analysis about the wellknown relationship between Alzheimer Demaentia outbreak and APP gene overexpression in Down young patients |
eedings |
Go to |
2004 |
OGM e nutrizione umana: dubbi e certezze. |
Articolo in rivista |
Go to |
2004 |
Hypercalciuria and kidney calcifications in terminal 4q deletion syndrome: further evidence for a putative gene on 4q. |
Articolo in rivista |
Go to |
2004 |
VRS ed asma: l'ipotesi immunogenica |
Articolo in rivista |
Go to |
2004 |
Marker cromosomico soprannumerario: iso 18p |
eedings |
Go to |
2004 |
SPREAD OF A NEW MBL-PRODUCING STRAIN OF PSEUDOMONAS AERUGINOSA IN NICU DURING MICROBIOLGICAL SURVEILLANCE IN 2003 |
eedings |
Go to |
2004 |
Colonizzazione da Gram negativi multiresistenti produttori di ESBL in una UTIN. |
eedings |
Go to |
2004 |
L’obesità nella Sindrome di Down: analisi di 320 soggetti in età evolutiva |
eedings |
Go to |
2004 |
Perché non bere e non fumare in gravidanza – Le conseguenze dell’alcool sul feto e sul neonato |
Articolo in rivista |
Go to |
2004 |
Colonizzazione da gram negativi multiresistenti produttori di beta-lattamasi ad ampio spettro (ESBL) in una UTIN. |
eedings |
Go to |
2004 |
Applicazione della PFGE nella sorveglianza da gram negativi multiresistenti in UTIN”, I Congresso Nazionale SIMPIOS; Bergamo, 20-22 maggio 2004 |
eedings |
Go to |
2004 |
La dimissione del neonato “ a rischio”. |
Articolo in rivista |
Go to |
2004 |
Patologia malformativa ed ostruzione nasale |
Capitolo o Saggio |
Go to |
2004 |
Il follow-up della sindrome di Down oggi: un modello esportabile. |
Articolo in rivista |
Go to |
2004 |
LA NUTRIZIONE PARENTERALE e L'INTESTINO RESIDUO: quale relazione nel decorso dei pazienti con Sindrome da Intestino Corto? Valutazione da una Casistica Nazionale Multicentrica |
eedings |
Go to |
2004 |
Mutation analysis of the ΔR 608 mutation causing Niemann-Pick disease type B from blood spot cards in sicilian people |
eedings |
Go to |
2004 |
Per riflettere su alcuni aspetti di bioetica intorno alla rianimazione
neonatale. |
Articolo in rivista |
Go to |
2004 |
Influenza dell’accrescimento in utero sui livelli plasmatici di Leptina, IGF-1 e IGF-BP3 |
eedings |
Go to |
2004 |
Sindrome Nefrosica Congenita di tipo Finlandese ed ipotiroidismo: descrizione di un caso |
eedings |
Go to |
2004 |
Infarto cerebrale in nato a termine:esiti a 12 mesi |
eedings |
Go to |
2004 |
Circolazione di Gram-negativi produttori di ESBL in una unità di terapia intensiva neonatale. |
eedings |
Go to |
2004 |
Prevenzione della patologia respiratoria virale nel neonato di bassissimo peso. |
Articolo in rivista |
Go to |
2004 |
Sindrome 13 q: intervento comportamentale e relazionale |
eedings |
Go to |
2004 |
17β-hydrossisteroid deydrogenase-3 deficiency (17 βHSD): clinical and endocrine features and molecular biology in two prepubertal patients |
eedings |
Go to |
2004 |
Pseudoacondroplasia: descrizione di un caso con piena espressività clinica |
eedings |
Go to |
2004 |
Colonizzazione da gram negativi multiresistenti produttori di ESBL in una UTIN”, I Congresso Nazionale SIMPIOS; Bergamo, 20-22 maggio 2004; |
eedings |
Go to |
2004 |
Variazioni delle frequenze degli alleli di ApoE in soggetti anziani ed in pazienti affetti da sindrome di Down. |
eedings |
Go to |
2004 |
Il Neonato con genitali ambigui: attivazione del Registro Nazionale del Protocollo Diagnostico Multidisciplinare della SIN |
eedings |
Go to |
2004 |
Rapid molecular diagnosis of Gilbert’s syndrome |
Articolo in rivista |
Go to |
2004 |
Sindrome del 13q intervento comportamentale e relazionale |
eedings |
Go to |
2004 |
Identification of a new nonsense mutation (Tyr129Stop) of the SRY gene in a newborn infant with XY sex-reversal |
Articolo in rivista |
Go to |
2004 |
Applicazione della PFGE nella sorveglianza delle colonizzazioni da gram negativi multiresistenti in UTIN |
eedings |
Go to |
2004 |
Severe neonatal onset of glycogenosis type IV: Clinical and laboratory findings leading to diagnosis in two siblings |
Articolo in rivista |
Go to |
2004 |
Newborn with oral, facial and digital abnormalities |
Articolo in rivista |
Go to |
2004 |
Perché non bere e non fumare in gravidanza – Le conseguenze del fumo sul feto e sul neonato |
Articolo in rivista |
Go to |
2004 |
EDEME GENERALIZZATO, IPOTONIA E IPERECCITABILITA' ALLA NASCITA IN NEONATO A TERMINE CON GALATTOSIALIDOSI:APPROCCIO CLINICO E DIAGNOSTICO |
eedings |
Go to |
2004 |
Spread of a new MBL-producing strani of Pseudomonas Aeruginosa in NICU during microbiological surveillance in 2003 |
eedings |
Go to |
2004 |
Diastematomelia:descrizione di un caso con quadro clinico peculiare |
eedings |
Go to |
2004 |
Trisomia 8 in mosaico: descrizione di un caso in epoca neonatale con piena espressività clinica. |
eedings |
Go to |
2004 |
Molecular analysis of the APP gene overexpression and his relationship with early onset of Alzheimer Dementia in young adults with Down Syndrome |
eedings |
Go to |
2004 |
Rara aneuploidia cromosomica, trisomia parziale 14 (q24.3_ter) de novo |
eedings |
Go to |
2004 |
Aracnodattilia contrattuale congenita (ACC) presentazione clinica in epoca neonatale. |
eedings |
Go to |
2004 |
Spread of a new MBL-producing strain of pseudomanas aeruginosa in NICU during microbiological surveillance in 2003 |
Articolo in rivista |
Go to |
2004 |
Colonizzazione da Gram negativi multiresistenti produttori di beta-lattamasi ad ampio spettro (ESBL) in una UTIN |
Altro |
Go to |
2004 |
PROTOCOLLO MULTIDISCIPLINARE DEI GENITALI AMBIGUI |
eedings |
Go to |
2004 |
Fish Odour Sindrome e deficit di GH: descrizione di una insolita associazione |
eedings |
Go to |
2004 |
Spread of a new MBL-producing strain of Pseudomonas aeruginosa in NICU during microbiological surbeillance in 2003 |
eedings |
Go to |
2004 |
DIAGNOSI DIFFERENZIALE DELLE POLMONITI VIRALI NEL NEONATO |
eedings |
Go to |
2002 |
Transposition of the great arteries and aortopulmonary window in the same patient: Clinical report and follow-up |
Articolo in rivista |
Go to |
1999 |
Maternal phenylketonuria in two Sicilian families identified by maternal blood phenylalanine level screening and identification of a new phenylalanine hydroxylase gene mutation (P407L) |
Lettera |
Go to |
1998 |
Monozygotic monoamniotic twins discordant for uretrhal and anal atresia with vesicorectal fistula: a favourable |
Articolo in rivista |
Go to |
1993 |
LA DIAGNOSTICA DELLE TUMEFAZIONI PELVICHE NELL'INFANZIE e NELL'ADOLESCENZA |
Articolo in rivista |
Go to |