Lipid deposition myopathy due to compound heterozygous mutation in the <i>ETFDH</i> gene: a case report. [PDF]
Li Y, Xiao G, Fu X, Jia J, Zheng Z.
europepmc +1 more source
Associations of one-carbon metabolism, related B-vitamins and ApoE genotype with cognitive function in older adults: identification of a novel gene-nutrient interaction. [PDF]
Gordon S+13 more
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Therapies for Mitochondrial Disease: Past, Present, and Future. [PDF]
Ball M+5 more
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Hepatic Form of Dihydrolipoamide Dehydrogenase Deficiency (DLDD): Phenotypic Spectrum, Laboratory Findings, and Therapeutic Approaches in 52 Patients. [PDF]
Hammann N+18 more
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The influence of a deficiency of vitamin B1 and of riboflavin on the reproduction of the rat
Katharine Hope Coward+2 more
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THE XANTHINE OXIDASE CONTENT OF RAT LIVER IN RIBOFLAVIN DEFICIENCY
A. E. Axelrod, C. A. Elvehjem
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Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency Presenting as Hyperammonemia and Encephalopathy: Case Series. [PDF]
Viguera Altolaguirre C+3 more
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Mitochondrial complex I deficiency in a 4-year-old boy due to compound heterozygous NDUFV1 mutation: a case report of a new pathogenic variant. [PDF]
Haddad S+8 more
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The Clinical and Biochemical Impact of the Multivitamin Shortage on Neonatal Patients. [PDF]
Frankel R+3 more
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The contribution of aquatic foods to human nutrient intake and adequacy in a small Island developing state. [PDF]
Zamborain-Mason J+10 more
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