Author:
Baal M. G.,Gabreëls F. J. M.,Renter W. O.,Hommes F. A.,Gijsbers Th. H. J.,Lamers K. J. B.,Kok J. C. N.
Subject
Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health
Reference23 articles.
1. Pyruvate carboxylase deficiency and lactic acidosis in à retarded child without Leigh's disease;Atkin;Pediatric Research,1979a
2. Pyruvate carboxylase and phosphoenolpyruvate carboxykinase activity in leucocytes and fibroblasts from à patient with pyruvate carboxylase deficiency;Utter;Pediatric Research,1979
3. Disorders of pyruvate metabolism;Blass;Neurology,1979
4. Thiamine-responsive lactic acidosis in a patient with deficient low-KM pyruvate carboxylase activity in liver;Brunette;Pediatrics,1972
5. Poliodystrophie cerebrale infantile (maladie ďAlpers) chez un nourrisson avec hyper-lactacidemie et anomalie de la pyruvate carboxylase hepatique;David;Archives Francoises de Pédiatrie,1975
Cited by
20 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Hypoglycemia;Genetic Diagnosis of Endocrine Disorders;2016
2. Pyruvate carboxylase deficiency: Mechanisms, mimics and anaplerosis;Molecular Genetics and Metabolism;2010-09
3. Metabolic Disorders;Developmental Medicine & Child Neurology;2008-11-12
4. Pyruvate Carboxylase Deficiency;Magnetic Resonance of Myelination and Myelin Disorders;2005
5. Treatment of pyruvate carboxylase deficiency with high doses of citrate and aspartate;American Journal of Medical Genetics;1999-12-03