Riboflavin-responsive glutaric aciduria type II presenting as a leukodystrophy

<scp>L</scp>‐2‐hydroxyglutaric acidemia: A novel inherited neurometabolic disease

P. G. Barth, Georg F. Hoffmann, J. Jaeken et al. · Annals of Neurology · 1992 · 151 citations

Life Sciences, Biochemistry, Neurology +15

C6—C10-Dicarboxylic Aciduria: Investigations of a Patient with Riboflavin Responsive Multiple Acyl-CoA Dehydrogenation Defects

N. Gregersen, H Wintzensen, Steen-Erik Christensen et al. · Pediatric Research · 1982 · 119 citations

Life Sciences, Biochemistry, Clinical Biochemistry +7

Fluorometric assay of acyl-CoA dehydrogenases in normal and mutant human fibroblasts

Frank E. Frerman, Stephen I. Goodman · Biochemical Medicine · 1985 · 114 citations

Life Sciences, Biochemistry, Molecular Biology +10

Glutaric acidaemia type II (multiple Acyl‐Coa dehydrogenation deficiency)

Stephen I. Goodman, Frank E. Frerman · Journal of Inherited Metabolic Disease · 1984 · 76 citations

Life Sciences, Genetics, Molecular Genetics +7

Normalization of short‐chain acylcoenzyme a dehydrogenase after riboflavin treatment in a girl with multiple acylcoenzyme a dehydrogenase—deficient myopathy

Stefano DiDonato, Cinzia Gellera, D. Peluchetti et al. · Annals of Neurology · 1989 · 53 citations

Life Sciences, Biochemistry, Pharmacology +17