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Original Articles

Sustained Attention in Untreated Non-PKU-Hyperphenylalaninemia

, , , &
Pages 343-348 | Accepted 29 Oct 1995, Published online: 04 Jan 2008

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L. Paermentier, A. Cano, B. Chabrol & A. Roy. (2023) Neuropsychological Disorders in Moderate Hyperphenylalaninemia: Literature Review. Developmental Neuropsychology 48:1, pages 31-45.
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Articles from other publishers (9)

Noushin Rostampour, Rojin Chegini, Silva Hovsepian, Farzaneh Zamaneh & Mahin Hashemipour. (2022) Cognitive function in untreated subjects with mild hyperphenylalaninemia: a systematic review. Neurological Sciences 43:9, pages 5593-5603.
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W.B. Hanley. (2011) Non-PKU mild hyperphenylalaninemia (MHP) — The dilemma. Molecular Genetics and Metabolism 104:1-2, pages 23-26.
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Francjan J. van Spronsen. (2011) Mild hyperphenylalaninemia: to treat or not to treat. Journal of Inherited Metabolic Disease 34:3, pages 651-656.
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JAUME CAMPISTOL, ROSA GASSIÓ, RAFAEL ARTUCH & Ma ANTONIA VILASECA. (2011) Neurocognitive function in mild hyperphenylalaninemia. Developmental Medicine & Child Neurology 53:5, pages 405-408.
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Dionísia Aparecida Cusin Lamônica, Mariana Germano Gejão, Amanda Tragueta Ferreira, Greyce Kelly da Silva & Fernanda da Luz Anastácio-Pessan. (2009) Desenvolvimento infantil na fenilcetonúria: atuação fonoaudiológica. Revista CEFAC 12:2, pages 326-330.
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Chuen-Der Kao, Dau-Ming Niu, Jen-Tse Chen, Din-E. Shan, Yung-Yang Lin, Zin-An Wu & Kwong-Kum Liao. (2004) Subtle brain dysfunction in treated 6-pyruvoyl-tetrahydropterin synthase deficiency: relationship to motor tasks and neurophysiological tests. Brain and Development 26:2, pages 93-98.
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Siegfried ZabranskyF. Haverkamp. 2001. Screening auf angeborene endokrine und metabole Störungen. Screening auf angeborene endokrine und metabole Störungen 218 225 .
. (2008) REFERENCES. Monographs of the Society for Research in Child Development 62:4, pages 194-205.
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. (1997) REFERENCES. Monographs of the Society for Research in Child Development 62:4, pages 194-205.
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