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Inclusion body myositis

Published:2014-11 Issue:6 Volume:26 Page:690-696
ISSN:1040-8711
Container-title:Current Opinion in Rheumatology
language:en
Short-container-title:

Author:

Lahouti Arash H.,Amato Anthony A.,Christopher-Stine Lisa

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Rheumatology

Reference35 articles.

1. The UDP-N-acetylglucosamine 2-epimeraseN-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy.;Eisenberg;Nat Genet,2001

2. Detecting dysphagia in inclusion body myositis.;Cox;J Neurol,2009

3. A 12-year follow-up in sporadic inclusion body myositis: an end stage with major disabilities.;Cox;Brain,2011

4. Long-term observational study of sporadic inclusion body myositis.;Benveniste;Brain,2011

5. Longitudinal observational study of sporadic inclusion body myositis: implications for clinical trials.;Cortese;Neuromuscul Disord,2013

Cited by 17 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Myosite à inclusions;Canadian Medical Association Journal;2024-07-28

2. Inclusion body myositis;Canadian Medical Association Journal;2024-04-14

3. Inflammatory Muscle Diseases;Clinical Immunology;2023

4. Hybrid Assistive Limb® for sporadic inclusion body myositis: A case series;Journal of Clinical Neuroscience;2020-11

5. Impact and Management of Dysphagia in Inflammatory Myopathies;Current Rheumatology Reports;2020-08-28

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