Amelioration of acylcarnitine profile using bezafibrate and riboflavin in a case of adult-onset glutaric acidemia type 2 with novel mutations of the electron transfer flavoprotein dehydrogenase (ETFDH) gene-Reference-Cited by-同舟云学术

Amelioration of acylcarnitine profile using bezafibrate and riboflavin in a case of adult-onset glutaric acidemia type 2 with novel mutations of the electron transfer flavoprotein dehydrogenase (ETFDH) gene

Published:2014-11 Issue:1-2 Volume:346 Page:350-352
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Shioya Ayako,Takuma Hiroshi,Yamaguchi Seiji,Ishii Akiko,Hiroki Masahiko,Fukuda Tokiko,Sugie Hideo,Shigematsu Yosuke,Tamaoka Akira

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

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

4. Clinical and molecular investigations of Japanese cases of glutaric acidemia type 2;Yotsumoto;Mol Genet Metab,2008

5. Bezafibrate can be a new treatment option for mitochondrial fatty acid oxidation disorders: evaluation by in vitro probe acylcarnitine assay;Yamaguchi;Mol Genet Metab,2012

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