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Pre-attentive processing in children with early and continuously-treated PKU. Effects of concurrent Phe level and lifetime dietary control

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Large neutral amino acids in the treatment of phenylketonuria (PKU)

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Remarkable differences: the course of life of young adults with galactosaemia and PKU

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Tetrahydrobiopterin availability, nitric oxide metabolism and glutathione status in the hph-1 mouse; implications for the pathogenesis and treatment of tetrahydrobiopterin deficiency states

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