Cardiomyopathy in Multiple Acyl-CoA Dehydrogenase Deficiency

Glutaric aciduria type II: Report on a previously undescribed metabolic disorder

Hildegard Przyrembel, U. Wendel, Kathrin Becker et al. · Clinica Chimica Acta · 1976 · 230 citations

Glomerular Disease, Metabolic Syndrome, Renal Function +10

Glutaric aciduria Type II

Lawrence Sweetman, William L. Nyhan, Doris A. Trauner et al. · The Journal of Pediatrics · 1980 · 213 citations

Glomerular Disease, Urology, Medicine +6

Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of life

Richard G. Boles, Elizabeth Buck, Miriam G. Blitzer et al. · The Journal of Pediatrics · 1998 · 203 citations

D,L-3-hydroxybutyrate treatment of multiple acyl-CoA dehydrogenase deficiency (MADD)

J L Van Hove, Stephanie Grünewald, Jaak Jaeken et al. · The Lancet · 2003 · 108 citations

Aldehyde Dehydrogenase, Biochemistry, Metabolism +3

Multiple Acyl-CoA Dehydrogenase Deficiency (Glutaric Aciduria Type II) with Transient Hypersarcosinemia and Sarcosinuria; Possible Inherited Deficiency of an Electron Transfer Flavoprotein

Stephen I. Goodman, Edward R.B. McCabe, Paul V. Fennessey et al. · Pediatric Research · 1980 · 102 citations · Full text

Possible Inherited Deficiency, Electron Transfer Flavoprotein, Metabolic Disorder +6