Subacute myopathy in a mature patient due to multiple acyl-coenzyme a dehydrogenase deficiency-Reference-Cited by-同舟云学术

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Subacute myopathy in a mature patient due to multiple acyl-coenzyme a dehydrogenase deficiency

Published:2011-02-14 Issue:3 Volume:43 Page:444-446
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Kaminsky Pierre,Acquaviva-Bourdain Cecile,Jonas Jacques,Pruna Lelia,Chaloub Gihan e,Rigal Odile,Grignon Yves,Vianey-Saban Christine

Publisher

Wiley

Subject

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

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mus.21881/fullpdf

Reference22 articles.

1. Glutaric aciduria type II: report on a previously undescribed metabolic disorder;Przyrembel;Clin Chem Acta,1976

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

3. Glutaric acidaemia type II (multiple acyl-CoA dehydrogenation deficiency);Goodman;J Inherit Metab Dis,1984

4. So doctor, what exactly is wrong with my muscles? Glutaric aciduria type II presenting in a teenager;Beresford;Neuromuscul Disord,2006

5. ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency;Olsen;Brain,2007

Cited by 8 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. ETF dehydrogenase advances in molecular genetics and impact on treatment;Critical Reviews in Biochemistry and Molecular Biology;2021-04-07

2. Lipid storage myopathies: Current treatments and future directions;Progress in Lipid Research;2018-10

3. Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic disease;Revue Neurologique;2016-03

4. Clinical, biochemical and molecular investigation of adult-onset glutaric acidemia type II: Characteristics in comparison with pediatric cases;Brain and Development;2016-03

5. Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency;Orphanet Journal of Rare Diseases;2014-07-22

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