Clinical and Electrophysiological Findings in Hereditary Inclusion Body Myopathy Compared With Sporadic Inclusion Body Myositis
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Clinical Neurology,Neurology,General Medicine
Reference37 articles.
1. Inclusion body myositis;Yunis;Lab Invest,1971
2. Working group, 188th ENMC International Workshop: inclusion body myositis, 2–4 December 2011, Naarden, The Netherlands;Rose;Neuromuscul Disord,2013
3. New advances in inclusion-body myositis;Askanas;Curr Opin Rheumatol,1993
4. Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein;Watts;Nat Genet,2004
5. Autosomal dominant myopathy: missense mutation (Glu-706--> Lys) in the myosin heavy chain IIa gene;Martinsson;Proc Natl Acad Sci U S A,2000
Cited by 13 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. Electromyography varies by stage in inclusion body myositis;Frontiers in Neurology;2024-01-05
2. Bialelic Pathogenic (c.830G>A(p.R277Q)) Variant Disrupting the GNE Gene Function and Causes Nonaka myopathy Phenotype;Cytology and Genetics;2023-07-27
3. Diagnostic delay of myositis: an integrated systematic review;Orphanet Journal of Rare Diseases;2022-11-21
4. Inclusion body myositis: Update on the diagnostic and therapeutic landscape;Frontiers in Neurology;2022-09-27
5. Anti‐cN1A antibodies do not correlate with specific clinical, electromyographic, or pathological findings in sporadic inclusion body myositis;Muscle & Nerve;2021-01-12
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3