Please use this identifier to cite or link to this item:
Title: Idiopathic myositis
Authors: Burgunder, J.-M. 
Issue Date: 2003
Citation: Burgunder, J.-M. (2003). Idiopathic myositis. Therapeutische Umschau 60 (7) : 407-412. ScholarBank@NUS Repository.
Abstract: The idiopathic myositis, dermatomyositis, polymyositis and inclusion body myositis are recognized by their clinical and laboratory presentation, and by morphological changes in the muscle biopsy. A rapid diagnostic process is important, in order to start early treatment, which will be more effective and to direct further investigations and management. In the presence of dermatomyositis a precise investigation of neoplasia is important because they are often associated, which is not the case with inclusion body myositis. Symptoms in dermatomyositis and polymyositis respond sometimes quite well to immunomodulatory therapy but not in inclusion myositis. Controlled muscle training may sometimes slow progression in inclusion myositis.
Source Title: Therapeutische Umschau
ISSN: 00405930
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.

Page view(s)

checked on May 22, 2019

Google ScholarTM


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.