Mitochondrial acetoacetyl-CoA thiolase deficiency
- 1 October 1986
- journal article
- research article
- Published by Elsevier in Biochemical Medicine and Metabolic Biology
- Vol. 36 (2), 198-206
- https://doi.org/10.1016/0885-4505(86)90125-8
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Biochemical investigations on a patient with a defect in cytosolic acetoacetyl‐CoA thiolase, associated with mental retardationJournal of Inherited Metabolic Disease, 1984
- Beta-ketothiolase deficiency in a family confirmed by in vitro enzymatic assays in fibroblastsEuropean Journal of Pediatrics, 1982
- The Presence of a New 3‐Oxoacyl‐CoA Thiolase in Rat Liver PeroxisomesEuropean Journal of Biochemistry, 1980
- Nephrotic syndrome in children: A randomized trial comparing two prednisone regimens in steroid-responsive patients who relapse earlyThe Journal of Pediatrics, 1979
- A Patient with Severe Neurologic Symptoms and Acetoacetyl-CoA Thiolase DeficiencyPediatric Research, 1977
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976
- Effect of oral alanine on blood beta-hydroxybutyrate and plasma glucose, insulin, free fatty acids, and growth hormone in normal and diabetic subjectsMetabolism, 1974
- Effects of oral alanine administration in fasting obese subjectsMetabolism, 1973
- The oxoacyl-coenzyme A thiolases of animal tissuesBiochemical Journal, 1973
- An Inherited Disorder of Isoleucine Catabolism Causing Accumulation of α-Methylacetoacetate and α-Methyl-β-hydroxybutyrate, and Intermittent Metabolic AcidosisPediatric Research, 1973