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SM ISO690:2012 UŞURELU, Natalia, GARAEVA, Svetlana, LÎSÎI, Leonid, ŢUREA, Valentin. Determinativele individualizării tratamentului dereglărilor metabolismului fenilalaninei
. In: Buletin de Perinatologie, 2009, nr. 3(43), pp. 219-228. ISSN 1810-5289. |
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Buletin de Perinatologie | ||||||
Numărul 3(43) / 2009 / ISSN 1810-5289 | ||||||
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Pag. 219-228 | ||||||
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Phenylketonuria (PKU) is an inborn poly-enzymatic multi-system pathology of the metabolism, its primary block being the Phenylalanine hydroxylation that leads
to severe mental retardation with clinical and biochemical polymorphism. 30 PKU children and 31 Phenylalanineuria children have been investigated for the level of
free amino acids in blood and urine. The troubles of the metabolism of Phe, Trp, Met, urea cycle and of enzyme transport systems on the kidney level were appreciated
in both studied lots. The effectiveness of the PKU treatment increases if combining the low Phe diet with drug metabolic correction on the base of free amino acids level
in blood and urine. |
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