Intelligence quotients and intelligence loss in patients with phenylketonuria and some variant states
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference29 articles.
1. Atypical phenylketonuria with normal or borderline intelligence;Hsia;Amer. J. Dis. Child.,1968
2. Causes for high phenylalanine with normal tyrosine in newborn screening programs;Berman;Amer. J. Dis. Child.,1969
3. Atypical phenylketonuric heterozygote;Anderson;J. Pediat.,1966
4. Diagnostic and therapeutic implications of persistent hyperphenylalaninemia in an infant heterozygous for the gene phenylketonuria;Schneider;J. Pediat.,1966
5. Phenylalaninemia;Auerbach,1968
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1. Non-PKU mild hyperphenylalaninemia (MHP) — The dilemma;Molecular Genetics and Metabolism;2011-09
2. Intellectual Development and Academic Achievement of Children Treated Early for Phenylketonuria;Developmental Medicine & Child Neurology;2008-11-12
3. Neuropsychological Functioning in Treated Phenylketonuria;The International Journal of Psychiatry in Medicine;1987-06
4. Histological maturation of the neocortex in phenylketonuric rats;Early Human Development;1983-07
5. Experimental hyperphenylalaninemia: Dendritic alterations in motor cortex of rat;Experimental Neurology;1981-10
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