Determinants of Riboflavin Responsiveness in Multiple Acyl-CoA Dehydrogenase Deficiency-Reference-Cited by-同舟云学术

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Determinants of Riboflavin Responsiveness in Multiple Acyl-CoA Dehydrogenase Deficiency

Published:2019-10 Issue: Volume:99 Page:69-75
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Yıldız Yılmaz,Talim Beril,Haliloglu Goknur,Topaloglu Haluk,Akçören Zuhal,Dursun Ali,Sivri Hatice Serap,Coşkun Turgay,Tokatlı Ayşegül

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health

Reference21 articles.

1. Riboflavin transport and metabolism in humans;Barile;J Inherit Metab Dis,2016

2. State of the art in muscle lipid diseases;Liang;Acta Myol,2010

3. Electron transfer flavoprotein deficiency: functional and molecular aspects;Schiff;Mol Genet Metab,2006

4. Brown-Vialetto-Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatment;Bosch;J Inherit Metab Dis,2011

5. Impaired riboflavin transport due to missense mutations in SLC52A2 causes Brown-Vialetto-Van Laere syndrome;Haack;J Inherit Metab Dis,2012

Cited by 21 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. Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study;Orphanet Journal of Rare Diseases;2024-01-14

2. Recognizing and Managing a Metabolic Crisis;Pediatric Clinics of North America;2023-10

3. Clinical and molecular investigation of 37 Japanese patients with multiple acyl-CoA dehydrogenase deficiency: p.Y507D in ETFDH, a common Japanese variant, causes a mortal phenotype;Molecular Genetics and Metabolism Reports;2022-12

4. Features and diagnostic value of body composition in patients with late-onset multiple acyl-CoA dehydrogenase deficiency;Acta Neurologica Belgica;2022-05-26

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

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