3-methylglutaconic aciduria in a patient with a disturbed mitochondrial energy metabolism
- 1 April 1992
- journal article
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 151 (4) , 313
- https://doi.org/10.1007/bf02072242
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Early fine motor and adaptive development in high-risk appropriate for gestational age preterm and healthy term childrenEuropean Journal of Pediatrics, 1991
- Phenotypic heterogeneity in the syndromes of 3-methylglutaconic aciduriaThe Journal of Pediatrics, 1991
- SIGNIFICANCE OF PRENATAL, PERINATAL AND POSTNATAL FACTORS IN THE DEVELOPMENT OF AGA PRETERM INFANTS AT FIVE TO SEVEN YEARSDevelopmental Medicine and Child Neurology, 1989
- 3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normalEuropean Journal of Pediatrics, 1988
- Episodes of severe metabolic acidosis in a patient with 3-methylglutaconic aciduriaEuropean Journal of Pediatrics, 1987