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

Springer Publishing Company

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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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Neuropsychological outcome of experimental manipulation of phenylalanine intake in treated phenylketonuria

By Griffiths P.   Ward N.   Harvie A.   Cockburn F.  

Journal of Inherited Metabolic Disease, Vol. 21, Iss. 1, 1998-01 ,pp. : 29-38

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Pathogenesis of different clinical outcomes in spite of identical genotypes and comparable blood phenylalanine concentrations in phenylketonurics

By Weglage J.   Wiedermann D.   Möller H.   Ullrich K.  

Journal of Inherited Metabolic Disease, Vol. 21, Iss. 2, 1998-04 ,pp. : 181-182

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Phenylalanine can be detected in brain tissue of healthy subjects by ¹H magnetic resonance spectroscopy

By Pietz J.   Pietz J.   Lutz T.   Zwygart K.   Hoffmann G. F.   Ebinger F.   Boesch C.   Kreis R.  

Journal of Inherited Metabolic Disease, Vol. 26, Iss. 7, 2003-01 ,pp. : 683-692

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