Correlations between branched-chain amino acids and branched-chain α-keto acids in blood in maple syrup urine disease-Reference-Cited by-同舟云学术

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Correlations between branched-chain amino acids and branched-chain α-keto acids in blood in maple syrup urine disease

Published:1978-09 Issue:2 Volume:88 Page:283-291
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Langenbeck U.,Wendel U.,Mench-Hoinowski Angelika,Kuschel D.,Becker K.,Przyrembel Hildegard,Bremer H.J.

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference34 articles.

1. Metabolism of the white blood cells in maple-syrup-urine disease

2. Defective decarboxylase in branched chain ketoacid oxidase multienzyme complex in classic type of maple syrup urine disease

3. Maple Syrup Urine Disease: Analysis of Branched Chain Ketoacid Decarboxylation in Cultured Fibroblasts

Cited by 69 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. Neonatal Screening for Inherited Metabolic Diseases in 2016;Seminars in Pediatric Neurology;2016-11

2. Evolution of maple syrup urine disease in patients diagnosed by newborn screening versus late diagnosis;European Journal of Paediatric Neurology;2015-11

3. Structural white matter changes in adolescents and young adults with maple syrup urine disease;Journal of Inherited Metabolic Disease;2013-01-25

4. HYPER-2-OXOGLUTARIC ACIDURIA IN LONG-TERM MENTAL HANDICAP;Journal of Intellectual Disability Research;2008-06-28

5. Dysmyelination in the brain of adolescents and young adults with maple syrup urine disease;Molecular Genetics and Metabolism;2004-05

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