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Article

Multiple acyl-coenzyme A dehydrogenation disorders (MAD) responsive to riboflavin: biochemical studies in fibroblasts.

Progress in clinical and biological research - 1 Jan 1992

Roettger V, Marshall T, Amendt B, Rhead W J

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Share to Acyl Coenzyme A
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 1438377

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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Multiple acyl-coenzyme A dehydrogenation disorders (MAD) responsive to riboflavin: biochemical studies in fibroblasts.PMID 1438377Read ↗

Short-chain and medium-chain acylCoA dehydrogenases are lowered in riboflavin-responsive lipid myopathies with multiple acylCoA dehydrogenase deficiency.Semantic proximity Read ↗

A Comparative study on riboflavin responsive multiple acyl-CoA dehydrogenation deficiency due to variants in FLAD1 and ETFDH geneSemantic proximity Read ↗

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Riboflavin-responsive multiple Acyl-CoA dehydrogenation deficiency in 13 cases, and a literature review in mainland Chinese patients.Semantic proximity Read ↗

New insights into the nutritional genomics of adult-onset riboflavin-responsive diseasesSemantic proximity Read ↗

Disorders of flavin adenine dinucleotide metabolism: MADD and related deficiencies.Semantic proximity Read ↗

ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.Semantic proximity Read ↗

Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case reportSemantic proximity Read ↗

Update on clinical aspects and treatment of selected vitamin-responsive disorders II (riboflavin and CoQ 10).Semantic proximity Read ↗

Genotype-environment interaction drives the onset of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency in carriers of single heterozygous ETFDH variants.Semantic proximity Read ↗

A comparative study on riboflavin responsive multiple acyl-CoA dehydrogenation deficiency due to variants in FLAD1 and ETFDH gene.Semantic proximity Read ↗

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