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
Hauptverfasser: Rozman, B, Božič, B, Kveder, T
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container_end_page 1005; discussion 1006
container_issue 8
container_start_page 1005
container_title Annals of the rheumatic diseases
container_volume 63
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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source MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central; Alma/SFX Local Collection
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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