Unusual presentations of propionic acidemia
- 30 November 1994
- journal article
- case report
- Published by Elsevier in Brain & Development
- Vol. 16, 46-57
- https://doi.org/10.1016/0387-7604(94)90096-5
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Emergency presentations of patients with methylmalonic acidemia, propionic acidemia and branched chain amino acidemia (MSUD)Brain & Development, 1994
- Comparative frequency and severity of hypoglycemia in selected organic acidemias, branched chain amino acidemia, and disorders of fructose metabolismBrain & Development, 1994
- Propionate mitochondrial toxicity in liver and skeletal muscle: Acyl CoA levelsBiochemical Medicine and Metabolic Biology, 1991
- Genetic heterogeneity of propionic acidemia: Analysis of 15 Japanese patientsHuman Genetics, 1991
- Tandem mass spectrometry: A new method for acylcarnitine profiling with potential for neonatal screening for inborn errors of metabolismJournal of Inherited Metabolic Disease, 1990
- Behavior management of feeding disturbances in urea cycle and organic acid disordersThe Journal of Pediatrics, 1987
- Newborn urine screening experience with over one million infants in the Quebec Network of Genetic MedicineJournal of Inherited Metabolic Disease, 1987
- Propionic acidemia: A clinical updateThe Journal of Pediatrics, 1981
- Asymptomatic propionyl CoA carboxylase deficiency in a 13-year-old girlThe Journal of Pediatrics, 1979
- The specificity of glycine-N-acylase and acylglycine excretion in the organicacidaemiasBiochemical Medicine, 1974