Factors affecting the variation in plasma phenylalanine in patients with phenylketonuria on diet.

Author:

MacDonald A,Rylance G,Hall S K,Asplin D,Booth I W

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference26 articles.

1. Phenylketonuria due to phenylalanine hydroxylase deficiency: an unfolding story;of Medical Research Council Working Party on Phenylketonuria, Report;BMJ,1993

2. Intelligence and quality of dietary treatment in phenylketonuria;Smith, I.; Beasley, M.; Ades, A.E.;Arch Dis Child,1990

3. Neuropsychology of early treated phenylketonuria: specific executive function deficits;Welsh, M.C.; Pennington, B.F.; Ozonoff, S.; Rouse, B.; McCabe, E.R.B.;Child Dev,1990

4. Decreased vigilance and neurotransmitter synthesis after discontinuation of dietary treatment of phenylketonuria in adolescents;Lou, H.C.; Guttler, G.; Lykkelund, C.; Bruhn, P.; Niederweiser, A.;EurJ Pediatr,1985

5. Neurological deficits in early-treated phenylketonurics;Pennington, B.F.; van B Doornick; WJ, McCabe; LL, McCabe; E.R.;Am J Ment Deficiency,1985

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