Literature DB >> 4708049

Phenylalanine loading and aromatic acid excretion in normal subjects and heterozygotes for phenylketonuria.

K Blau, G K Summer, H C Newsome, C H Edwards.   

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Year:  1973        PMID： 4708049     DOI： 10.1016/0009-8981(73)90427-0

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN： 0009-8981            Impact factor:   3.786


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  6 in total

1.  A synopsis of the unconjugated acidic transamination metabolites of phenylalanine in phenylketonuria.

Authors:  U Langenbeck; A Behbehani; A Mench-Hoinowski
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

2.  Quantitative analysis of phenylalanine metabolites in urine to detect heterozygotes of phenylketonuria.

Authors:  K Olek; K Oyanagi; P Wardenbach
Journal:  Humangenetik       Date:  1974-04-24

3.  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

4.  Examination of urine metabolites in the newborn period and during protein loading tests at 6 months of age--Part 1.

Authors:  E Mönch; J Kneer; C Jakobs; M Arnold; H Diehl; U Batzler
Journal:  Eur J Pediatr       Date:  1990       Impact factor: 3.183

5.  Phenylketonuria heterozygote detection in families with affected children.

Authors:  T D Paul; I K Brandt; L J Elsas; C E Jackson; P Mamunes; C S Nance; W E Nance
Journal:  Am J Hum Genet       Date:  1978-05       Impact factor: 11.025

6.  Phenylalanine and UVA light for the treatment of vitiligo.

Authors:  R H Cormane; A H Siddiqui; W Westerhof; R B Schutgens
Journal:  Arch Dermatol Res       Date:  1985       Impact factor: 3.017
  6 in total

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