Concepedia

Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acids

Marinus Durán, Grant Mitchell, Johannis B.C. de Klerk, J. P. de Jager, Marchinus Hofkamp, L. Bruinvis, D. Ketting, Jean‐Marie Saudubray, S.K. Wadman

The Journal of Pediatrics · 1985 · 46 citations · 24 references

DOI

Concepts

References

24

The Cerebrohepatorenal (Zellweger) Syndrome

Ann E. Moser, Inderjit Singh, Frank R. Brown et al. · New England Journal of Medicine · 1984 · 271 citations

, , +14

Systemic Carnitine Deficiency — A Treatable Inherited Lipid-Storage Disease Presenting as Reye's Syndrome

P Chapoy, C. Angelini, Wendy J. Brown et al. · New England Journal of Medicine · 1980 · 248 citations

, , +10

Adrenoleukodystrophy: Impaired Oxidation of Very Long Chain Fatty Acids in White Blood Cells, Cultured Skin Fibroblasts, and Amniocytes

Inderjit Singh, Ann E. Moser, Hugo W. Moser et al. · Pediatric Research · 1984 · 239 citations

, , +17

Jamaican Vomiting Sickness

Kay Tanaka, Eccleston A. Kean, Barbara Johnson · New England Journal of Medicine · 1976 · 209 citations

, , +8

Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Children with Non-Ketotic Hypoglycemia and Low Carnitine Levels

Charles A. Stanley, Daniel E. Hale, Paul M. Coates et al. · Pediatric Research · 1983 · 197 citations

, , +9