Literature DB >> 21377827

Observations on the classification of the inflammatory myopathies.

David Hilton-Jones1.   

Abstract

This brief review considers historical approaches to the classification of the inflammatory myopathies. The last 25 years have seen advances in our knowledge of the underlying immune mechanism but the initial trigger for the idiopathic inflammatory myopathies remains unknown. Existing classifications have their limitations, but with the absence of a "gold standard" a definitive classification is not yet possible. Despite these problems, a working classification is possible that is valuable for everyday clinical practice.
Copyright © 2011 Elsevier Masson SAS. All rights reserved.

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Year:  2011        PMID: 21377827     DOI: 10.1016/j.lpm.2010.10.035

Source DB:  PubMed          Journal:  Presse Med        ISSN: 0755-4982            Impact factor:   1.228


  4 in total

1.  Clinico pathological study of adult dermatomyositis: Importance of muscle histology in the diagnosis.

Authors:  Sudhir Babu Karri; Meena Anga Muthu Kannan; Liza Rajashekhar; Megha S Uppin; Sundaram Challa
Journal:  Ann Indian Acad Neurol       Date:  2015 Apr-Jun       Impact factor: 1.383

2.  Hypercapnic respiratory failure during pregnancy due to polymyositis-related respiratory muscle weakness: a case report.

Authors:  Husain Shabbir Ali; Ibrahim Fawzy Hassan; Saibu George; Abdalrazig Elsadig Fadlelmula
Journal:  J Med Case Rep       Date:  2017-07-26

3.  Increased prevalence of celiac disease in idiopathic inflammatory myopathies.

Authors:  Olof Danielsson; Björn Lindvall; Claes Hallert; Magnus Vrethem; Charlotte Dahle
Journal:  Brain Behav       Date:  2017-09-05       Impact factor: 2.708

Review 4.  STAT3 in Skeletal Muscle Function and Disorders.

Authors:  Eleonora Guadagnin; Davi Mázala; Yi-Wen Chen
Journal:  Int J Mol Sci       Date:  2018-08-02       Impact factor: 5.923

  4 in total

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