Neonatal onset of medium-chain Acyl-CoA dehydrogenase deficiency in two siblings-Reference-Cited by-同舟云学术

Neonatal onset of medium-chain Acyl-CoA dehydrogenase deficiency in two siblings

Published:1988-01 Issue:2 Volume:10 Page:129-134
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Nobukuni Yoshitaka,Yokoo Tetsuya,Ohtani Yoshinobu,Endo Fumio,Aoki Shigeru,Yoshinaga Muneyoshi,Matsumoto Takashi,Yoshimoto Masaaki,Tsuji Yoshiro,Matsuda Ichiro

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference29 articles.

1. Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels;Stanley;Pediatr Res,1983

2. Deficiency of medium-chain fatty acyl-coenzyme A dehydrogenase presenting as the sudden infant death syndrome;Howat;Br Med J,1984

3. Medium-chain acyl-CoA dehydrogenase deficiency in two siblings with a Reye-like syndrome;Bougneres;J Pediatr,1985

4. Genetic deficiency of medium-chain acyl coenzyme A dehydrogenase: studies in cultured skin fibroblasts and peripheral mononuclear leukocytes;Coates;Pediatr Res,1985

5. Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromes;Roe;J Pediatr,1986

Cited by 11 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

1. Screening for medium-chain acyl CoA dehydrogenase deficiency: current perspectives;Research and Reports in Neonatology;2016-01

2. Disorders of Organic Acid Metabolism;Neurology of the Newborn;2008

3. Neonatal hypoglycaemia and withdrawal symptoms after exposure in utero to valproate;Archives of Disease in Childhood - Fetal and Neonatal Edition;2000-09-01

4. Fatty acid oxidation disorders as primary cause of sudden and unexpected death in infants and young children: an investigation performed on cultured fibroblasts from 79 children who died aged between 0-4 years.;Molecular Pathology;1997-08-01

5. Frequency of 985A-to-G mutation in medium-chain acyl-CoA dehydrogenase gene among patients with sudden infant death syndrome, Reye syndrome, severe motor and intellectual disabilities and healthy newborns in Japan;Pediatrics International;1996-08