Multiple Acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothers-Reference-Cited by-同舟云学术

Multiple Acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothers

Published:1982-09 Issue:1 Volume:139 Page:60-65
ISSN:0340-6199
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

B�hm N.,Uy J.,Kie�ling M.,Lehnert W.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/BF00442082.pdf

Reference7 articles.

1. Gregersen N (1979) Studies on the effect of saturated and unsaturated short-chain monocarboxylic acids on the energy metabolism of rat liver mitochondria. Pediatr Res 13:1227?1230

2. Gregersen N, Kolvraa S, Rasmussen K, Christensen E, Brandt NJ, Ebbesen F (1980) Biochemical studies in a patient with defects in the metabolism of acyl-CoA and sarcosine: Another possible case of glutaric aciduria type II. J Inher Metab Dis 3:67?72

3. Hird FJR, Weidemann MJ (1966) Oxidative phosphorylation accompanying oxidation of short-chain fatty acids by rat liver mitochondria. Biochem J 98:378?388

4. Landing BH (1974) Considerations of the pathogenesis of neonatal hepatitis, biliary atresia and choledochal cyst. The concept of infantile obstructive cholangiopathy. Prog Pediatr Surg 6:113?139

5. Osathanondh V, Potter EL (1964) Pathogenesis of polycystic kidneys. Arch Pathol 77:459?512

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