Mitochondrial Short-Chain L-3-Hydroxyacl-Coenzyme A Dehydrogenase Deficiency: A New Defect of Fatty Acid Oxidation

Hypoglycemic Disorders

1995 • 473 citations

Fatty acid oxidation disorders: A new class of metabolic diseases

1992 • 178 citations

A comparison of [9,10‐³H]palmitic and [9,10‐³H]myristic acids for the detection of defects of fatty acid oxidation in intact cultured fibroblasts

1989 • 153 citations

Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acidβ‐oxidation

1990 • 121 citations

Hypoglycemia in infancy and childhood. Part II

1973 • 111 citations

Ketotic hypoglycemia

1964 • 97 citations

Short‐chain<scp>L</scp>‐3‐hydroxyacyl‐CoA dehydrogenase deficiency in muscle: A new cause for recurrent myoglobinuria and encephalopathy

1991 • 84 citations

The L-3-hydroxyacyl-CoA dehydrogenase deficiency.

1990 • 52 citations

Intact α-Subunit Is Required for Membrane Binding of Human Mitochondrial Trifunctional β-Oxidation Protein, but Is Not Necessary for Conferring 3-Ketoacyl-CoA Thiolase Activity to the β-Subunit

1995 • 22 citations

Ketonuria and medium‐chain acyl‐CoA dehydrogenase deficiency

1995 • 12 citations

The enzymes of mitochondrial fatty acid oxidation

1994 • 12 citations