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Systemic sclerosis - a systematic overview: part 1 - disease characteristics and classification, pathophysiologic concepts, and recommendations for diagnosis and surveillance.
Klein-Weigel, P; Opitz, C; Riemekasten, G.
Afiliação
  • Klein-Weigel P; Klinik für Innere Medizin, Schwerpunkt Angiologie und kardiovaskuläre Frührehabilitation, DRK Kliniken Berlin, Germany. p.klein-weigel@drk-kliniken-berlin.de
Vasa ; 40(1): 6-19, 2011 Jan.
Article em En | MEDLINE | ID: mdl-21283969
ABSTRACT
Due to its high association with Raynaud's phenomenon systemic sclerosis (SSc) is probably the most common connective tissue disease seen by vascular specialists. In part 1 of our systematic overview we summarize classification concepts of scleroderma disorders, the epidemiologic and genetic burden, the complex pathophysiologic background, and the clinical features and the stage-dependent capillary microscopic features of SSc. Furthermore, we address the diagnostic recommendations propagated by the German Network for Systemic Sclerosis and the Task Force for Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology, the European Respiratory Society, and the International Society of Heart and Lung Transplantation.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Raynaud / Escleroderma Sistêmico / Úlcera / Hipertensão Pulmonar Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Humans País/Região como assunto: Europa Idioma: En Revista: Vasa Ano de publicação: 2011 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Raynaud / Escleroderma Sistêmico / Úlcera / Hipertensão Pulmonar Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Humans País/Região como assunto: Europa Idioma: En Revista: Vasa Ano de publicação: 2011 Tipo de documento: Article