Skin sclerosis is only of limited value to identify SSc patients with severe manifestations--an analysis of a distinct patient subgroup of the German Systemic Sclerosis Network (DNSS) Register.

Hanitsch, L G; Burmester, G-R; Witt, C; Hunzelmann, N; Genth, E; Krieg, T; Lehmacher, W; Melchers, I; Meurer, M; Müller-Ladner, U; Schulze-Lohoff, E; Becker, M; Sunderkoetter, C; Riemekasten, G

Hanitsch, L G; Burmester, G-R; Witt, C; Hunzelmann, N; Genth, E; Krieg, T; Lehmacher, W; Melchers, I; Meurer, M; Müller-Ladner, U; Schulze-Lohoff, E; Becker, M; Sunderkoetter, C; Riemekasten, G.

Affiliation

Hanitsch LG; Clinic of Rheumatology and Clinical Immunology, Charité Universitätsmedizin, Charité, Berlin, Germany.

Rheumatology (Oxford) ; 48(1): 70-3, 2009 Jan.

Article in En | MEDLINE | ID: mdl-19056798

Subject(s)

Scleroderma, Systemic/pathology; Skin/pathology; Cohort Studies; Contracture/etiology; Deglutition Disorders/etiology; Humans; Hypertension, Pulmonary/etiology; Pulmonary Fibrosis/etiology; Scleroderma, Diffuse/complications; Scleroderma, Diffuse/pathology; Scleroderma, Systemic/complications; Severity of Illness Index; Skin Ulcer/etiology; Time Factors

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Scleroderma, Systemic / Skin Type of study: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Humans Language: En Journal: Rheumatology (Oxford) Year: 2009 Document type: Article

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