Individualized long-term outcomes in blood phenylalanine concentrations and dietary phenylalanine tolerance in 11 patients with primary phenylalanine hydroxylase (PAH) deficiency treated with Sapropterin-dihydrochloride-Reference-Cited by-同舟云学术

Individualized long-term outcomes in blood phenylalanine concentrations and dietary phenylalanine tolerance in 11 patients with primary phenylalanine hydroxylase (PAH) deficiency treated with Sapropterin-dihydrochloride

Published:2015-03 Issue:3 Volume:114 Page:409-414
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Stockler-Ipsiroglu Sylvia,Yuskiv Nataliya,Salvarinova Ramona,Apatean Delia,Ho Gloria,Cheng Barbara,Giezen Alette,Lillquist Yolanda,Ueda Keiko

Funder

CIHR

Publisher

Elsevier BV

Subject

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

Reference44 articles.

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3. National Institutes of Health Consensus Development Conference Statement: Phenylketonuria: screening and management, October 16–18, 2000;Pediatrics,2001

4. Rationale for the German recommendations for Phenylalanine level control in Phenylketonuria 1997;Burgard;Eur. J. Pediatr.,1999

5. Review: emotional and behavioral functioning in Phenylketonuria;Sullivan;J. Pediatr. Psychol.,1999

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