Pyruvate carboxylase deficiency: clinical and biochemical response to anaplerotic diet therapy
- 30 April 2005
- journal article
- case report
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 84 (4) , 305-312
- https://doi.org/10.1016/j.ymgme.2004.09.007
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Pyruvate carboxylase deficiency—insights from liver transplantationMolecular Genetics and Metabolism, 2002
- The Key Role of Anaplerosis and Cataplerosis for Citric Acid Cycle FunctionJournal of Biological Chemistry, 2002
- In vivo13C NMR measurement of neurotransmitter glutamate cycling, anaplerosis and TCA cycle flux in rat brain during [2‐13C]glucose infusionJournal of Neurochemistry, 2001
- Anaplerosis of the citric acid cycle: role in energy metabolism of heart and skeletal muscleActa Physiologica Scandinavica, 2000
- Recent Developments in the Investigation of Inherited Metabolic Disorders Using Cultured Human CellsMolecular Genetics and Metabolism, 1999
- Glucose and ketone body utilization by the brain of neonatal ratsProgress in Neurobiology, 1993
- Brain amino acid abnormalities in pyruvate carboxylase deficiencyJournal of Inherited Metabolic Disease, 1984
- Comparative measurements of glucose, beta-hydroxybutyrate, acetoacetate, and insulin in blood and cerebrospinal fluid during starvationMetabolism, 1974
- CEREBRAL ARTERIO‐VENOUS DIFFERENCE OF ACETOACETATE AND D‐β‐HYDROXYBUTYRATE IN CHILDRENActa Paediatrica, 1972
- Brain Metabolism during Fasting*Journal of Clinical Investigation, 1967