Pearls & Oy-sters: A curable myopathy manifesting as exercise intolerance and respiratory failure-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Pearls & Oy-sters: A curable myopathy manifesting as exercise intolerance and respiratory failure

Published:2018-07-23 Issue:4 Volume:91 Page:187-190
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Silva André M.S.,Mendonça Rodrigo H.,Soares Diogo C.,Callegaro Dagoberto,Caldas Vitor M.,Perissinotti Iago N.,Carvalho Mary S.,Zanoteli Edmar

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Reference14 articles.

1. ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency

2. Clinical and genetic analysis of lipid storage myopathies

3. Late-onset multiple acyl-CoA dehydrogenase deficiency: A frequently missed diagnosis?

4. Fatty acid oxidation defects presenting as primary myopathy and prominent dropped head syndrome;Vengalil;Neuromuscul Disord,2017

5. Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic disease;Béhin;Rev Neurol,2016

Cited by 5 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. Disease spectrum of myopathies with elevated aldolase and normal creatine kinase;European Journal of Neurology;2023-11-03

2. Generation of a human induced pluripotent stem cell line (LZUSHi002-A) from a MADD patient with ETFDH mutation;Stem Cell Research;2022-10

3. Features and diagnostic value of body composition in patients with late-onset multiple acyl-CoA dehydrogenase deficiency;Acta Neurologica Belgica;2022-05-26

4. A systematic review of late-onset and very-late-onset multiple acyl-coenzyme A dehydrogenase deficiency: Cohort analysis and patient report from Taiwan;Neuromuscular Disorders;2021-03

5. Genetic cause of heterogeneous inherited myopathies in a cohort of Greek patients;Molecular Genetics and Metabolism Reports;2020-12

同舟云学术

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