Clinical risk assessment of organ manifestations in systemic sclerosis: a report from the EULAR Scleroderma Trials And Research group database

Walker, U; Tyndall, A; Czirják, L; Denton, C; Farge-Bancel, D; Kowal-Bielecka, O; Müller-Ladner, U; Bocelli-Tyndall, C; Matucci-Cerinic, M

doi:10.1136/ard.2006.062901

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Title		Clinical risk assessment of organ manifestations in systemic sclerosis: a report from the EULAR Scleroderma Trials And Research group database
Authors		Walker, U Tyndall, A Czirják, L Denton, C Farge-Bancel, D Kowal-Bielecka, O Müller-Ladner, U Bocelli-Tyndall, C Matucci-Cerinic, M show all authors [1 - 9]
Collaboration		EUSTAR With : Ribi, Camillo / Chizzolini, Carlo
Published in		Annals of the rheumatic diseases. 2007, vol. 66, no. 6, p. 754-63
Abstract		Systemic sclerosis (SSc) is a multisystem autoimmune disease, which is classified into a diffuse cutaneous (dcSSc) and a limited cutaneous (lcSSc) subset according to the skin involvement. In order to better understand the vascular, immunological and fibrotic processes of SSc and to guide its treatment, the EULAR Scleroderma Trials And Research (EUSTAR) group was formed in June 2004.
Keywords		Adult — Age Distribution — Age of Onset — Aged — Autoantibodies/blood — Cross-Sectional Studies — Databases, Factual — Female — Humans — Male — Middle Aged — Nuclear Proteins/immunology — Raynaud Disease/etiology/immunology — Risk Assessment — Scleroderma, Diffuse/complications/immunology — Scleroderma, Limited/complications/immunology — Scleroderma, Systemic/complications/immunology — Sex Factors
Identifiers		DOI: 10.1136/ard.2006.062901 PMID: 17234652
Full text		Article (Published version) (340 Kb) - Free access
Structures		Faculté de médecine / Section de médecine clinique / Département de médecine
Research group		La matrice extracellulaire (651)
Citation (ISO format)		WALKER, U et al. Clinical risk assessment of organ manifestations in systemic sclerosis: a report from the EULAR Scleroderma Trials And Research group database. In: Annals of the rheumatic diseases, 2007, vol. 66, n° 6, p. 754-63. doi: 10.1136/ard.2006.062901 https://archive-ouverte.unige.ch/unige:73762