Author:
Jakobs C.,Sweetman L.,Wadman S. K.,Duran M.,Saudubray J.-M.,Nyhan W. L.
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Reference20 articles.
1. Böhm N, Uy J, Kiessling M, Lehnert W (1982) Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two brothers. II. Morphology and pathogenesis. Eur J Pediatr 139:60?65
2. Coudé FX, Ogier H, Charpentier C, Thomassin G, Checoury A, Amedeemanesme O, Saudubray JM, Frezal J (1981) Neonatal glutaric aciduria type II: an X-linked recessive inherited disorder. Hum Genet 59:263?265
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. Pediatr Res 14:12?17
4. Goodman SI, Gallegos DA, Pullin CH, Halpern B, Truscott RJW, Wise G, Wilcken B, Ryan ED, Whelan DT (1980) Antenatal diagnosis of glutaric acidemia. Am J Hum Genet 32:695?699
5. Goodman SI, Stene DO, McCabe ERB, Norenberg MD, Shikes RH, Stumpf DA, Blackburn GC (1982) Glutaric acidemia type II: clinical, biochemical and morphological considerations. J Pediatr 100:946?950
Cited by
38 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