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

Published:1982-09 Issue:1 Volume:139 Page:56-59
ISSN:0340-6199
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

Lehnert W.,Wendel U.,Lindenmaier S.,B�hm N.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/BF00442081.pdf

Reference16 articles.

1. Christensen E: Personal communication

2. Dusheiko G, Kew CM, Joffe BJ, Lewin JR, Path FF, Mantagos S, Tanaka K (1979) Recurrent hypoglycemia associated with glutaric aciduria type II in an adult. N Engl J Med 301:1405?1409

3. Goodman SI, McCabe ERB, Fennessey PV, Mace JW (1980) Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; Possible inherited deficiency of an electron transfer flavoprotein. Pediat Res 14:12?17

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

5. Lehnert W, Schuchmann L, Urbánek R, Niederhoff H, Böhm N (1978) Excretion of 2-Methyl-3-oxovaleric acid in propionic acidemia. Eur J Pediatr 128:197?205

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