Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic disease-Reference-Cited by-同舟云学术

Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic disease

Published:2016-03 Issue:3 Volume:172 Page:231-241
ISSN:0035-3787
Container-title:Revue Neurologique
language:en
Short-container-title:Revue Neurologique

Author:

Béhin A.,Acquaviva-Bourdain C.,Souvannanorath S.,Streichenberger N.,Attarian S.,Bassez G.,Brivet M.,Fouilhoux A.,Labarre-Villa A.,Laquerrière A.,Pérard L.,Kaminsky P.,Pouget J.,Rigal O.,Vanhulle C.,Eymard B.,Vianey-Saban C.,Laforêt P.

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference31 articles.

1. Diagnosis, treatment, and long-term outcomes of late-onset (type III) multiple acyl-CoA dehydrogenase deficiency;Pollard;J Child Neurol,2010

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

3. Glutaric acidemia type II: gene structure and mutations of the electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) gene;Goodman;Mol Genet Metab,2002

4. Subacute myopathy in a mature patient due to multiple acyl-coenzyme A dehydrogenase deficiency;Kaminsky;Muscle Nerve,2011

5. Déficit multiple en acyl-CoA déshydrogénases : une cause traitable de lipidose musculaire d’origine génétique;Maillart;Rev Neurol (Paris),2010

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