Therapeutic trial in the first three Asian cases of ethylmalonic encephalopathy: Response to riboflavin-Reference-Cited by-同舟云学术

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Therapeutic trial in the first three Asian cases of ethylmalonic encephalopathy: Response to riboflavin

Published:2001-12 Issue:8 Volume:24 Page:870-873
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Yoon H-R.¹,Hahn S. H.²,Ahn Y. M.³,Jang S. H.³,Shin Y. J.³,Lee E. H.²,Ryu K. H.²,Eun B. L.⁴,Rinaldo P.⁵,Yamaguchi S.⁶

Affiliation:

1. Metabolic Disease Detection Laboratory; Seoul Medical Science Institute; Seoul

2. ; Department of Pediatrics; Ajou University School of Medicine; Suwon

3. Department of Pediatrics; Kangnam General Hospital; Seoul Korea

4. ; Korea University School of Medicine; Seoul Korea

5. ; Biochemical Genetics Laboratory; Mayo Clinic; Rochester Minnesota USA

6. ; Department of Pediatrics; Shimane Medical University; Japan

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1013948409790/fullpdf

Reference3 articles.

1. New clinical phenotype of branched-chain acyl-CoA oxidation defect;Burlina;Lancet,1991

2. A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblasts;Burlina;J Pediatr,1994

3. Newly identified forms of electron transfer flavoprotein deficiency in two patients with glutaric aciduria type II;Seiji;Pediatr Res,1991

Cited by 19 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. Ethylmalonic Encephalopathy: a literature review and two new cases of mild phenotype;Neurological Sciences;2023-07-17

2. Ethylmalonic encephalopathy: Phenotype-genotype description and review of its management;NEUROLOGIA;2021

3. Encefalopatía etilmalónica: descripción fenotipo-genotipo y revisión de su manejo;Neurología;2021-11

4. Ethylmalonic encephalopathy: phenotype-genotype description and review of its management;Neurología (English Edition);2021-11

5. Riboflavin Deficiency—Implications for General Human Health and Inborn Errors of Metabolism;International Journal of Molecular Sciences;2020-05-28

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