3-Hydroxy-3-methylglutaryl coenzyme A lyase deficiency: Postnatal management following prenatal diagnosis by analysis of maternal urine
- 31 December 1979
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 95 (6) , 1004-1007
- https://doi.org/10.1016/s0022-3476(79)80297-8
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- β-HYDROXY-β-METHYLGLUTARICACIDURIA PRESENTING AS REYE'S SYNDROMEThe Lancet, 1979
- Lethal hypoglycemia in a child with a deficiency of 3-hydroxy-3-methylglutarylcoenzyme A lyaseThe Journal of Pediatrics, 1979
- Organic acid excretion in a patient with 3-hydroxy-3-methylglutaryl-Coa lyase deficiency: Facts and artefactsClinica Chimica Acta; International Journal of Clinical Chemistry, 1978
- 3-hydroxy-3-methylglutaric aciduria: 3-Hydroxy-3-methylglutaryl-coenzyme a lyase levels in leucocytesClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- 3-hydroxy-3-methylglutaric aciduria: Deficiency of 3-hydroxy-3-methylglutaryl coenzyme a lyaseClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- 3-Hydroxy-3-methylglutaric aciduria, combined with 3-methylglutaconic aciduriaClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- Patient with Defect in Leucine MetabolismNew England Journal of Medicine, 1976