Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiency-Reference-Cited by-同舟云学术

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Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiency

Published:2007-09 Issue:1-2 Volume:92 Page:109-114
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Chiong M.A.,Sim K.G.,Carpenter K.,Rhead W.,Ho G.,Olsen R.K.J.,Christodoulou J.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference38 articles.

1. Defects of electron transfer flavoprotein and electron transfer flavoprotein–ubiquinone oxidoreductase: glutaric acidemia typeII;Frerman,2001

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

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

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

5. Glutaric aciduria types I and II;Gordon;Brain Dev.,2006

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1. Revitalising Riboflavin: Unveiling Its Timeless Significance in Human Physiology and Health;Foods;2024-07-17

2. New insights into the nutritional genomics of adult-onset riboflavin-responsive diseases;Nutrition & Metabolism;2023-10-16

3. Riboflavin 1 Transporter Deficiency: Novel SLC52A1 Variants and Expansion of the Phenotypic Spectrum;Genes;2023-07-07

4. Misdiagnosis of Total Parental Nutrition-Related Riboflavin Deficiency: Three Case Reports of Diagnostic Error;American Journal of Perinatology Reports;2023-01

5. Riboflavin deficiency due to vitamin shortage in neonates with parenteral nutrition dependence;Molecular Genetics and Metabolism;2022-09

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