Principali pubblicazioni del C.R.R. per le malattie rare reumatologiche
Ascolta
- Registri multicentrici: AIDA (AutoInflammatory Disease Alliance) Network, Osservatorio Malattie Rare.
- Centro afferente al Gruppo Italiano di Ricerca in Reumatologia Clinica e Sperimentale (GIRRCS)
- Collaborazione con il Gruppo di Ricerca sulle Vasculiti (SIR)
- Progetto FOREUM (Foundation for Research in Rheumatology) supportato dall’EULAR: "START – Molecular stratification of patients with giant cell arteritis to tailor glucocorticoid and tocilizumab therapy»
- Progetti interni di ricerca pre-clinica su SSc e Vasculiti
PRINCIPALI PUBBLICAZIONI (2020-2022)
- Rizzo C, La Barbera L, Miceli G, Tuttolomondo A and Guggino G (2022), The innate face of Giant Cell Arteritis: Insight into cellular and molecular innate immunity pathways to unravel new possible biomarkers of disease. Front. Mol. Med. 2:933161.
- Conticini E, d'Alessandro M, Grazzini S, Fornaro M, Sabella D, Lopalco G, Giardina F, Colafrancesco S, Rizzo C, Guggino G, Priori R, Conti F, Iannone F, Bargagli E, Cantarini L, Frediani B. Relapses of idiopathic inflammatory myopathies after vaccination against COVID-19: a real-life multicenter Italian study. Intern Emerg Med. 2022 Jun 26:1–8. doi: 10.1007/s11739-022-03028-3.
- La Barbera L, Macaluso F, Fasano S, Grasso G, Ciccia F, Guggino G. Microbiome Changes in Connective Tissue Diseases and Vasculitis: Focus on Metabolism and Inflammation. Int J Mol Sci. 2022 Jun 10;23(12):6532.
- Di Cola I, Di Muzio C, Conforti A, Iacono D, Pantano I, Rozza G, Rossi S, De Stefano L, Vitale A, Caso F, Costa L, Prete M, Navarini L, Iagnocco A, Atzeni F, Guggino G, Perosa F, Cantarini L, Frediani B, Bugatti S, Montecucco C, Ciccia F, Giacomelli R, Cipriani P, Ruscitti P. Adult-onset Still's disease with elderly onset, results from a multicentre study. Clin Exp Rheumatol. 2022 May 4.
- Scaturro D, Guggino G, Terrana P, Vitagliani F, Falco V, Cuntrera D, Benedetti MG, Moretti A, Iolascon G, Letizia Mauro G. Rehabilitative interventions for ischaemic digital ulcers, pain, and hand functioning in systemic sclerosis: a prospective before-after study. BMC Musculoskelet Disord. 2022 Mar 2;23(1):193.
- Ruscitti P, Natoli V, Consolaro A, Caorsi R, Rosina S, Giancane G, Naddei R, Di Cola I, Di Muzio C, Berardicurti O, Iacono D, Pantano I, Rozza G, Rossi S, De Stefano L, Balduzzi S, Vitale A, Caso F, Costa L, Prete M, Navarini L, Iagnocco A, Atzeni F, Guggino G, Perosa F, Cantarini L, Frediani B, Montecucco C, Ciccia F, Cipriani P, Gattorno M, Giacomelli R, Ravelli A. Disparities in the prevalence of clinical features between systemic juvenile idiopathic arthritis and adult-onset Still's disease. Rheumatology (Oxford). 2022 Jan 25:keac027.
- Ruscitti P, Di Cola I, Berardicurti O, Conforti A, Iacono D, Pantano I, Rozza G, Rossi S, De Ludovico S, Balduzzi S, Vitale A, Caso F, Costa L, Prete M, Navarini L, Atzeni F, Guggino G, Perosa F, Cantarini L, Frediani B, Montecucco C, Ciccia F, Giacomelli R, Cipriani P. Impact of smoking habit on adult-onset Still's disease prognosis, findings from a multicentre observational study. Clin Rheumatol. 2022 Mar;41(3):641-647.
- Colaci M, Schinocca C, Bosco YD, Ronsivalle G, Guggino G, de Andres I, Russo AA, Sambataro D, Sambataro G, Malatino L. Heart Valve Abnormalities in Systemic Sclerosis Patients: A Multicenter Cohort Study and Review of the Literature. J Clin Rheumatol. 2022 Jan 1;28(1):e95-e101.
- Di Benedetto P, Cipriani P, Iacono D, Pantano I, Caso F, Emmi G, Grembiale RD, Cantatore FP, Atzeni F, Perosa F, Scarpa R, Guggino G, Ciccia F, Giacomelli R, Ruscitti P. Ferritin and C-reactive protein are predictive biomarkers of mortality and macrophage activation syndrome in adult onset Still's disease. Analysis of the multicentre Gruppo Italiano di Ricerca in Reumatologia Clinica e Sperimentale (GIRRCS) cohort. PLoS One. 2020 Jul 9;15(7):e0235326.
- Ruscitti P, Berardicurti O, Iacono D, Pantano I, Liakouli V, Caso F, Emmi G, Grembiale RD, Cantatore FP, Atzeni F, Perosa F, Scarpa R, Guggino G, Ciccia F, Barile A, Cipriani P, Giacomelli R. Parenchymal lung disease in adult onset Still's disease: an emergent marker of disease severity-characterisation and predictive factors from Gruppo Italiano di Ricerca in Reumatologia Clinica e Sperimentale (GIRRCS) cohort of patients. Arthritis Res Ther. 2020 Jun 22;22(1):151.
- Colaci M, Dal Bosco Y, Schinocca C, Ronsivalle G, Guggino G, De Andres I, Russo AA, Sambataro D, Sambataro G, Malatino L. Aortic root dilation in associated with the reduction in capillary density observed at nailfold capillaroscopy in SSc patients. Clin Rheumatol. 2021 Mar;40(3):1185-1189.
- Di Benedetto P, Guggino G, Manzi G, Ruscitti P, Berardicurti O, Panzera N, Grazia N, Badagliacca R, Riccieri V, Vizza CD, Radchenko G, Liakouli V, Ciccia F, Cipriani P, Giacomelli R. Interleukin-32 in systemic sclerosis, a potential new biomarker for pulmonary arterial hypertension. Arthritis Res Ther. 2020 Jun 1;22(1):127.
- Pirrello R, Verro B, Grasso G, Ruscitti P, Cordova A, Giacomelli R, Ciccia F, Guggino G. Hyaluronic acid and platelet-rich plasma, a new therapeutic alternative for scleroderma patients: a prospective open-label study. Arthritis Res Ther. 2019 Dec 13;21(1):286.
Articoli su iris.unipa.it relative a malattie rare reumatologiche
Ascolta
Crioglobulinemia mista | Mixed cryoglobulinemia |
Behcet malattia di | Behcet's disease |
Endocardite reumatica | Rheumatic endocarditis |
Poliangioite microscopica | Microscopic polyangiitis |
Poliarterite nodosa | Polyarteritis nodosa |
Granulomatosi eosinofilica con poliangite | Eosinophilic granulomatosis with polyangiitis |
Goodpasture sindrome di | Goodpasture syndrome |
Granulomatosi con poliangite | Granulomatosis with polyangiitis |
Arterite a cellule giganti | Giant cell arteritis |
Microangiopatie trombotiche | Thrombotic microangiopathies |
Porpora trombotica trombocitopenica | Thrombotic thrombocytopenic purpura |
Takayasu malattia di | Takayasu's disease |
Teleangectasia emorragica ereditaria | Hereditary hemorrhagic telangiectasia |
Budd-Chiari sindrome di | Budd-Chiari syndrome |
Porpora di Henoch-Schoenlein ricorrente | Recurrent Henoch-Schoenlein purpura |
Linfedemi primari cronici | Chronic primary lymphoedema |
Linfedema ereditario di tipo 1 | Type 1 hereditary lymphedema |
Linfedema ereditario di tipo 2 | Type 2 hereditary lymphedema |
Linfedema idiopatico | Idiopathic lymphedema |
Linfedema primitivo autosomico recessivo | Primary autosomal recessive lymphoedema |
Sindrome delle unghie gialle | Yellow nail syndrome |
Dermatomiosite | Dermatomyositis |
Polimiosite | Polymyositis |
Sindrome da anticorpi antisintetasi | Antisynthetase antibody syndrome |
Connettivite mista | Mixed connectivity |
Fascite eosinofila | Eosinophilic fasciitis |
Fascite diffusa | Widespread fasciitis |
Policondrite ricorrente | Recurrent polychondritis |
Angiomatosi cistica diffusa dell’osso | Diffuse cystic angiomatosis of bone |
Eteroplasia ossea progressiva | Progressive bone heteroplasia |
Fibrodisplasia ossificante progressiva | Fibrodysplasia Ossificans Progressiva |
Meloreostosi | Meloreostosis |
Miosite a corpi inclusi | Inclusion body myositis |
Miosite eosinofila idiopatica | Idiopathic eosinophilic myositis |
Sclerosi sistemica progressiva | Progressive systemic sclerosis |
Sindrome SAPHO | SAPHO syndrome |
Articoli su pubmed.ncbi.nlm.nih.gov inerenti le malattie rare reumatologiche
Ascolta
Crioglobulinemia mista | Mixed cryoglobulinemia |
Behcet malattia di | Behcet's disease |
Endocardite reumatica | Rheumatic endocarditis |
Poliangioite microscopica | Microscopic polyangiitis |
Poliarterite nodosa | Polyarteritis nodosa |
Granulomatosi eosinofilica con poliangite | Eosinophilic granulomatosis with polyangiitis |
Goodpasture sindrome di | Goodpasture syndrome |
Granulomatosi con poliangite | Granulomatosis with polyangiitis |
Arterite a cellule giganti | Giant cell arteritis |
Microangiopatie trombotiche | Thrombotic microangiopathies |
Porpora trombotica trombocitopenica | Thrombotic thrombocytopenic purpura |
Takayasu malattia di | Takayasu's disease |
Teleangectasia emorragica ereditaria | Hereditary hemorrhagic telangiectasia |
Budd-Chiari sindrome di | Budd-Chiari syndrome |
Porpora di Henoch-Schoenlein ricorrente | Recurrent Henoch-Schoenlein purpura |
Linfedemi primari cronici | Chronic primary lymphoedema |
Linfedema ereditario di tipo 1 | Type 1 hereditary lymphedema |
Linfedema ereditario di tipo 2 | Type 2 hereditary lymphedema |
Linfedema idiopatico | Idiopathic lymphedema |
Linfedema primitivo autosomico recessivo | Primary autosomal recessive lymphoedema |
Sindrome delle unghie gialle | Yellow nail syndrome |
Dermatomiosite | Dermatomyositis |
Polimiosite | Polymyositis |
Sindrome da anticorpi antisintetasi | Antisynthetase antibody syndrome |
Connettivite mista | Mixed connectivity |
Fascite eosinofila | Eosinophilic fasciitis |
Fascite diffusa | Widespread fasciitis |
Policondrite ricorrente | Recurrent polychondritis |
Angiomatosi cistica diffusa dell’osso | Diffuse cystic angiomatosis of bone |
Eteroplasia ossea progressiva | Progressive bone heteroplasia |
Fibrodisplasia ossificante progressiva | Fibrodysplasia Ossificans Progressiva |
Meloreostosi | Meloreostosis |
Miosite a corpi inclusi | Inclusion body myositis |
Miosite eosinofila idiopatica | Idiopathic eosinophilic myositis |
Sclerosi sistemica progressiva | Progressive systemic sclerosis |
Sindrome SAPHO | SAPHO syndrome |
Articoli su onlinelibrary.wiley.com inerenti le malattie rare reumatologiche
Ascolta
Crioglobulinemia mista | Mixed cryoglobulinemia |
Behcet malattia di | Behcet's disease |
Endocardite reumatica | Rheumatic endocarditis |
Poliangioite microscopica | Microscopic polyangiitis |
Poliarterite nodosa | Polyarteritis nodosa |
Granulomatosi eosinofilica con poliangite | Eosinophilic granulomatosis with polyangiitis |
Goodpasture sindrome di | Goodpasture syndrome |
Granulomatosi con poliangite | Granulomatosis with polyangiitis |
Arterite a cellule giganti | Giant cell arteritis |
Microangiopatie trombotiche | Thrombotic microangiopathies |
Porpora trombotica trombocitopenica | Thrombotic thrombocytopenic purpura |
Takayasu malattia di | Takayasu's disease |
Teleangectasia emorragica ereditaria | Hereditary hemorrhagic telangiectasia |
Budd-Chiari sindrome di | Budd-Chiari syndrome |
Porpora di Henoch-Schoenlein ricorrente | Recurrent Henoch-Schoenlein purpura |
Linfedemi primari cronici | Chronic primary lymphoedema |
Linfedema ereditario di tipo 1 | Type 1 hereditary lymphedema |
Linfedema ereditario di tipo 2 | Type 2 hereditary lymphedema |
Linfedema idiopatico | Idiopathic lymphedema |
Linfedema primitivo autosomico recessivo | Primary autosomal recessive lymphoedema |
Sindrome delle unghie gialle | Yellow nail syndrome |
Dermatomiosite | Dermatomyositis |
Polimiosite | Polymyositis |
Sindrome da anticorpi antisintetasi | Antisynthetase antibody syndrome |
Connettivite mista | Mixed connectivity |
Fascite eosinofila | Eosinophilic fasciitis |
Fascite diffusa | Widespread fasciitis |
Policondrite ricorrente | Recurrent polychondritis |
Angiomatosi cistica diffusa dell’osso | Diffuse cystic angiomatosis of bone |
Eteroplasia ossea progressiva | Progressive bone heteroplasia |
Fibrodisplasia ossificante progressiva | Fibrodysplasia Ossificans Progressiva |
Meloreostosi | Meloreostosis |
Miosite a corpi inclusi | Inclusion body myositis |
Miosite eosinofila idiopatica | Idiopathic eosinophilic myositis |
Sclerosi sistemica progressiva | Progressive systemic sclerosis |
Sindrome SAPHO | SAPHO syndrome |