Classical maple syrup urine disease and brain development: Principles of management and formula design-Reference-Cited by-同舟云学术

Classical maple syrup urine disease and brain development: Principles of management and formula design

Published:2010-04 Issue:4 Volume:99 Page:333-345
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Strauss Kevin A.,Wardley Bridget,Robinson Donna,Hendrickson Christine,Rider Nicholas L.,Puffenberger Erik G.,Shelmer Diana,Moser Ann B.,Morton D. Holmes

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference78 articles.

1. Branched-chain ketoacyl dehydrogenase deficiency: maple syrup disease;Strauss;Curr. Treat. Options Neurol.,2003

2. Pediatric medicine and the genetic disorders of the Amish and Mennonite people of Pennsylvania;Morton;Am. J. Med. Genet. C Semin. Med. Genet.,2003

3. Maple Syrup Urine Disease;Strauss,2006

4. Abnormal dendritic development in maple syrup urine disease;Kamei;Pediatr. Neurol.,1992

5. Blood–brain barrier amino acid transport;Smith,1998

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