Neonatal-onset propionic acidemia: Neurologic and developmental profiles, and implications for management
- 30 June 1995
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 126 (6) , 916-922
- https://doi.org/10.1016/s0022-3476(95)70208-3
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Physiology and pathophysiology of organic acids in cerebrospinal fluidJournal of Inherited Metabolic Disease, 1993
- Neurologic outcome of propionic acidemiaPediatric Neurology, 1992
- In vivo propionate oxidation as a prognostic indicator in disorders of propionate metabolismEuropean Journal of Pediatrics, 1990
- Adult‐onset chorea and dementia with propionic acidemiaNeurology, 1989
- Behavior management of feeding disturbances in urea cycle and organic acid disordersThe Journal of Pediatrics, 1987
- Long term outcome of organic acidurias: Survey of 105 French cases (1967–1983)Journal of Inherited Metabolic Disease, 1984
- The management and long term outcome of organic acidaemiasJournal of Inherited Metabolic Disease, 1984
- Propionic acidemia: A clinical updateThe Journal of Pediatrics, 1981
- Asymptomatic propionyl CoA carboxylase deficiency in a 13-year-old girlThe Journal of Pediatrics, 1979
- Possible explanation for hyperglycinaemia in propionic acidaemia and methylmalonic acidaemia: Propionate and methylmalonate inhibit liver and brain mitochondrial glycine transportJournal of Inherited Metabolic Disease, 1979