Concepedia

Reye-like syndrome resulting from novel missense mutations in mitochondrial medium- and short-chain l-3-hydroxy-acyl-CoA dehydrogenase

Malcolm J. Bennett, L. RUSSELL, Chonan Tokunaga, Shilpa Narayan, Lina Tan, Adam C. Seegmiller, Richard L. Boriack

Molecular Genetics and Metabolism · 2006 · 34 citations · 14 references

DOI

Concepts

References

14

Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of β-oxidation in insulin secretion

Peter T. Clayton, Simon Eaton, A Aynsley‐Green et al. · Journal of Clinical Investigation · 2001 · 252 citations · Full text

, , +15

Familial Hyperinsulinemic Hypoglycemia Caused by a Defect in the SCHAD Enzyme of Mitochondrial Fatty Acid Oxidation

Anders Molven, Guri E. Matre, Marinus Durán et al. · Diabetes · 2004 · 204 citations · Full text

, , +17

Human trifunctional protein deficiency: A new disorder of mitochondrial fatty acid β-oridation

Ronald J. A. Wanders, Lodewijk IJlst, F Poggi et al. · Biochemical and Biophysical Research Communications · 1992 · 154 citations

, , +16

Biochemical Characterization and Crystal Structure Determination of Human Heart Short Chain <scp>l</scp>-3-Hydroxyacyl-CoA Dehydrogenase Provide Insights into Catalytic Mechanism

Joseph Barycki, Laurie K. O'Brien, Judy M. Bratt et al. · Biochemistry · 1999 · 95 citations

, , +17

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

Ingrid Tein, Darryl C. De Vivo, Daniel E. Hale et al. · Annals of Neurology · 1991 · 84 citations

, , +12