[Phenylalanine hydroxylase activity in the liver in children with the classic form of phenylketonuria].

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作者信息

Shaposhnikov A M, Barashnev Iu I, Khal'chitskiĭ S E, Korneĭchuk V V, Okat'ev V S

出版信息

Vopr Okhr Materin Det. 1978 Jun;23(6):42-7.

PMID:676196

Abstract

摘要

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[Phenylalanine hydroxylase activity in the liver in children with the classic form of phenylketonuria].

Vopr Okhr Materin Det. 1978 Jun;23(6):42-7.

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相似文献

[Phenylalanine hydroxylase activity in the liver in children with the classic form of phenylketonuria].

Vopr Okhr Materin Det. 1978 Jun;23(6):42-7.

Determination of phenylalanine hydroxylase activity in patients with phenylketonuria and hyperphenylalaninemia.

Pediatr Res. 1975 Dec;9(12):899-903. doi: 10.1203/00006450-197512000-00006.

Phenylketonuria and its variants.

West J Med. 1979 Oct;131(4):324-6.

[Phenylalanine hydroxylase activity in the livers of patients with phenylketonuria].

Vopr Med Khim. 1974 Nov-Dec;20(6):656-60.

Atypical phenylketonuria with normal phenylalanine hydroxylase and dihydropteridine reductase activity in vitro.

Pediatrics. 1977 May;59(5):757-61.

Detection of hepatic phenylalanine 4-hydroxylase in classical phenylketonuria.

Proc Natl Acad Sci U S A. 1973 Feb;70(2):552-6. doi: 10.1073/pnas.70.2.552.

[Phenylalanine hydroxylase activity in hyperphenyl-alaninemia and classical phenylketonuria].

Acta Biol Med Ger. 1972;28(3):549-52.

Diagnosis of phenylalanine hydroxylase deficiency (phenylketonuria).

Am J Dis Child. 1982 Feb;136(2):111-4. doi: 10.1001/archpedi.1982.03970380023006.

[Genetical heterogeneity of phenylketonuria].

Vopr Med Khim. 1982 May-Jun;28(3):62-70.

Phenylalanine hydroxylase expression in liver of a fetus with phenylketonuria.

J Pediatr. 1988 Sep;113(3):463-8. doi: 10.1016/s0022-3476(88)80629-2.