Idiopathiás inflammatoricus myositisek alcsoportjainak, kórlefolyásának és kimenetelének tanulmányozása

Translated title of the contribution: Characteristics of different subsets and long-term outcome in patients with idiopathic inflammatory myositis

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Abstract

The heterogeneous group of idiopathic inflammatory myositis (IIM) consists of rare systemic autoimmune diseases. The hallmark of these disorders is the autoimmune process mediated progressive weakness of the proximal muscles. The Dermatomyositis/Polymyositis Outpatient Clinic has been started its activity in 1985 at the 3rd Department of Internal Medicine, University of Debrecen. Since then, more than 300 patients has been diagnosed and followed up. Our aim was the critical analysis of clinical aspects of IIMs in these patients, focusing on the clinical course, survival, medium- and long-term functional outcome and quality of life, and to evaluate patients with uncommon forms of IIMs, such as juvenile and cancer-associated myositis.

Original languageHungarian
Pages (from-to)7-16
Number of pages10
JournalOrvoskepzes
Volume80
Issue number1
Publication statusPublished - Dec 1 2005

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ASJC Scopus subject areas

  • Medicine(all)

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