Nonketotic Hyperglycinemia (Glycine Encephalopathy): Laboratory Diagnosis
- 1 September 2001
- journal article
- review article
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 74 (1-2) , 139-146
- https://doi.org/10.1006/mgme.2001.3224
Abstract
No abstract availableKeywords
This publication has 50 references indexed in Scilit:
- Neonatal type of nonketotic hyperglycinemiaPediatric Neurology, 1999
- Depletion of Cerebral D-Serine in Non-Ketotic Hyperglycinemia: Possible Involvement of Glycine Cleavage System in Control of Endogenous D-SerineBiochemical and Biophysical Research Communications, 1997
- Prognostic clues and outcome of early treatment of nonketotic hyperglycinemiaPediatric Neurology, 1996
- Nonketotic hyperglycinemia: Atypical clinical and biochemical manifestationsThe Journal of Pediatrics, 1996
- Atypical nonketotic hyperglycinemia confirmed by assay of the glycine cleavage system in lymphoblastsThe Journal of Pediatrics, 1993
- Neurologic sequelae in transient nonketotic hyperglycinemia of the neonateThe Journal of Pediatrics, 1992
- Enzymatic diagnosis of nonketotic hyperglycinemia with lymphoblastsThe Journal of Pediatrics, 1992
- Prenatal diagnosis of nonketotic hyperglycinemia: Enzymatic analysis of the glycine cleavage system in chorionic villiThe Journal of Pediatrics, 1990
- Transient nonketotic hyperglycinemia in neonatesThe Journal of Pediatrics, 1989
- A decrease in glycine cleavage activity in the liver of a patient with dihydrolipoyl dehydrogenase deficiencyJournal of Inherited Metabolic Disease, 1986