Interstitial lung disease, a common manifestation of newly diagnosed polymyositis and dermatomyositis
The discrepancy between the results in our patients and previously presented data is likely to depend on the different methods that have been used in different studies. 2 The patient cohort presented in our study is small, which makes analyses from stratified patient groups into subgroups such as po...
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Veröffentlicht in: | Annals of the rheumatic diseases 2004-08, Vol.63 (8), p.1005-1005; discussion 1006 |
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container_title | Annals of the rheumatic diseases |
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creator | Rozman, B Božič, B Kveder, T |
description | The discrepancy between the results in our patients and previously presented data is likely to depend on the different methods that have been used in different studies. 2 The patient cohort presented in our study is small, which makes analyses from stratified patient groups into subgroups such as polymyositis or dermatomyositis uncertain. |
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subjects | Antigens Autoantibodies - blood dermatomyositis Dermatomyositis - immunology Enzyme-Linked Immunosorbent Assay - methods Enzymes Humans Immunoassay Immunoglobulins Laboratories lung disease Lung diseases Lung Diseases, Interstitial - immunology Matters Arising Patients polymyositis Studies |
title | Interstitial lung disease, a common manifestation of newly diagnosed polymyositis and dermatomyositis |
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