Multiple Acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothers
- 1 September 1982
- journal article
- case report
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 139 (1), 60-65
- https://doi.org/10.1007/bf00442082
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
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- Glutaric aciduria type II: Report on a previously undescribed metabolic disorderClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- Considerations of the pathogenesis of neonatal hepatitis, biliary atresia and choledochal cyst--the concept of infantile obstructive cholangiopathy.1974
- Oxidative phosphorylation accompanying oxidation of short-chain fatty acids by rat-liver mitochondriaBiochemical Journal, 1966
- PATHOGENESIS OF POLYCYSTIC KIDNEYS. HISTORICAL SURVEY.1964