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

Springer Publishing Company

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

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

Springer Publishing Company

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Unexpectedly low asymmetric dimethylarginine (ADMA) and homocysteine levels in patients with phenylketonuria(PKU)

By Özcan Ömer  

Journal of Inherited Metabolic Disease, Vol. 35, Iss. 6, 2012-11 ,pp. : 1153-1153

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Efficacy and safety of BH4 before the age of 4 years in patients with mild phenylketonuria

By Leuret Oriane   Barth Magalie   Kuster Alice   Eyer Didier   Parscau Loïc   Odent Sylvie   Gilbert-Dussardier Brigitte   Feillet François   Labarthe François  

Journal of Inherited Metabolic Disease, Vol. 35, Iss. 6, 2012-11 ,pp. : 975-981

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Developmental Defects of Enamel in Phenylketonuria Patients

By de Marco Salvadori Carina   Pereira Rosana Marques   Raichert Caroline   de Morais Ferreira Fernanda   de Menezes José Vitor Nogara Borges  

Journal of Dentistry for Children, Vol. 81, Iss. 3, 2014-12 ,pp. : 147-150

American Academy of Pediatric Dentistry

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