Literature DB >> 5655958

Heterogeneity in genetic control of phenylalanine metabolism in man.

D Rosenblatt, C R Scriver.   

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Year:  1968        PMID: 5655958     DOI: 10.1038/218677a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


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  17 in total

1.  Letter: Screening for phenylketonuria.

Authors: 
Journal:  Br Med J       Date:  1974-02-09

Review 2.  Phenylketonuria and its variations. A review of recent developments.

Authors:  M E Blaskovics; T L Nelson
Journal:  Calif Med       Date:  1971-07

3.  Classic phenylketonuria: heterozygote detection during pregnancy.

Authors:  R F Griffin; M E Humienny; E C Hall; L J Elsas
Journal:  Am J Hum Genet       Date:  1973-11       Impact factor: 11.025

4.  The efficacy of dietary therapy for phenylketonuria.

Authors:  W B Hanley; L S Linsao; C Netley
Journal:  Can Med Assoc J       Date:  1971-06-19       Impact factor: 8.262

5.  Molecular biology of phenylketonuria.

Authors:  F Güttler; A G DiLella; F D Ledley; A S Lidsky; S C Kvok; J Marvit; S L Woo
Journal:  Eur J Pediatr       Date:  1987       Impact factor: 3.183

6.  Plasma phenylalanine and tyrosine levels revisited in heterozygotes for hyperphenylalaninaemia.

Authors:  J M Saraiva; J W Seakins; I Smith
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

7.  Detection of phenylketonuria carriers.

Authors:  S Kelly; F Rose
Journal:  Public Health Rep       Date:  1969-02       Impact factor: 2.792

8.  Severity of mutation in the phenylalanine hydroxylase gene influences phenylalanine metabolism in phenylketonuria and hyperphenylalaninaemia heterozygotes.

Authors:  E Svensson; L Iselius; L Hagenfeldt
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

9.  Heterozygous carriers of classical phenylketonuria in a sample of the Turkish population: detection by a spectrofluorimetric method.

Authors:  F Güneral; I Ozalp; H Tatlidil
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

Review 10.  The influence of mutations of enzyme activity and phenylalanine tolerance in phenylalanine hydroxylase deficiency.

Authors:  F Güttler; P Guldberg
Journal:  Eur J Pediatr       Date:  1996-07       Impact factor: 3.183

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