Correlation of age-specific phenylalanine levels with intellectual outcome in patients with phenylketonuria

By Viau Krista   Wengreen Heidi   Ernst Sharon   Cantor Nancy   Furtado Larissa   Longo Nicola  

Journal of Inherited Metabolic Disease, Vol. 34, Iss. 4, 2011-08 ,pp. : 963-971

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Frontal lobe-dependent functions in treated phenylketonuria: Blood phenylalanine concentrations and long-term deficits in adolescents young adults

By Feldmann R.   Denecke J.   Grenzebach M.   Weglage J.  

Journal of Inherited Metabolic Disease, Vol. 28, Iss. 4, 2005-06 ,pp. : 445-455

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In vitro read-through of phenylalanine hydroxylase (PAH) nonsense mutations using aminoglycosides: a potential therapy for phenylketonuria

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Journal of Inherited Metabolic Disease, Vol. 36, Iss. 6, 2013-11 ,pp. : 955-959

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In vivo NMR spectroscopy in patients with phenylketonuria: Clinical significance of interindividual differences in brain phenylalanine concentrations

By Weglage J.   Möller H.E.   Wiedermann D.   Cipcic-Schmidt S.   Zschocke J.   Ullrich K.  

Journal of Inherited Metabolic Disease, Vol. 21, Iss. 1, 1998-01 ,pp. : 81-82

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The course of life and quality of life of early and continuously treated Dutch patients with phenylketonuria

By Bosch A.   Tybout W.   Spronsen F.   Valk H.   Wijburg F.   Grootenhuis M.  

Journal of Inherited Metabolic Disease, Vol. 30, Iss. 1, 2007-02 ,pp. : 29-34

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