Fulminant lipid storage myopathy due to multiple acyl-coenzyme a dehydrogenase deficiency-Reference-Cited by-同舟云学术

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Fulminant lipid storage myopathy due to multiple acyl-coenzyme a dehydrogenase deficiency

Published:2015-02-11 Issue:2 Volume:52 Page:289-293
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Whitaker Charles H.¹,Felice Kevin J.¹,Silvers David²,Wu Qian³

Affiliation:

1. Department of Neuromuscular Medicine; Hospital for Special Care; 2150 Corbin Avenue New Britain Connecticut 06053 USA

2. Department of Neurology; Hartford Hospital; Hartford Connecticut USA

3. Deparment of Pathology; University of Connecticut Health Center; Farmington Connecticut USA

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Reference24 articles.

1. Lipid storage myopathies;Bruno;Curr Opin Neurol,2008

2. Disorders of muscle lipid metabolism: diagnostic and therapeutic challenges;Laforet;Neuromuscul Disord,2010

3. Clear relationship between ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency;Olsen;Hum Mutat,2003

Cited by 23 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. Mit Schluckstörungen assoziierte Erkrankungen;Praxiswissen Logopädie;2024

2. Case report: A novel c.1842_1845dup mutation of ETFDH in two Chinese siblings with multiple acyl-CoA dehydrogenase deficiency;Frontiers in Pediatrics;2023-01-04

3. Metabolic and Mitochondrial Myopathies;Clues for Differential Diagnosis of Neuromuscular Disorders;2023

4. Diagnostic Challenges in Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: Clinical, Morphological, and Genetic Aspects;Frontiers in Neurology;2022-03-03

5. The clinical, pathological, and genetic characteristics of lipid storage myopathy in northern China;Turkish Journal of Medical Sciences;2022-01-01

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