Another Population of Phenylketonuria? Studies on Atypical Phenylketonurias-Reference-Cited by-同舟云学术

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Another Population of Phenylketonuria? Studies on Atypical Phenylketonurias

Published:2008-11-12 Issue:6 Volume:11 Page:718-729
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:

Author:

Dyken Paul,Culley William

Publisher

Wiley

Subject

Clinical Neurology,Developmental Neuroscience,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1969.tb01515.x/fullpdf

Reference11 articles.

1. Procedures for monitoring the low-phenylalanine diet in treatment of phenylketonuria;Berry;J. Pediat.,1965

2. Cognitive development and dietary therapy in phenylketonuric children;Dobson;New Engl. J. Med.,1968

3. Uber Ausscheidung von Phenylbrenztraubensaure in den Ham als Stoffwechselanomalie in Verbindung mit Imbezillitat;Foiling;Z. physiol. Chem.,1934

4. Atypical phenylketonuria with borderline or normal intelligence;Hsia;Amer. J. Dis. Child.,1968

Cited by 3 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. Historical aspects and overview of research on phenylketonuria;Mental Retardation and Developmental Disabilities Research Reviews;1999

2. Mental Retardation;Psychiatrie der Gegenwart;1972

3. The Myth of Perfectibility;The Journal of Special Education;1970-07

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