Literature DB >> 4379218

Atypical phenylketonuric heterozygote. Deficiency in phenylalanine hydroxylase and transaminase activity.

J A Anderson, R Fisch, E Miller, D Doeden.   

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Year:  1966        PMID: 4379218     DOI: 10.1016/s0022-3476(66)80237-8

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


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  7 in total

1.  Set of simple side-room urine tests for detection of inborn errors of metabolism.

Authors:  N R Buist
Journal:  Br Med J       Date:  1968-06-22

2.  Phenylalaninaemia. Differential diagnosis.

Authors:  M E Blaskovics; G E Schaeffler; S Hack
Journal:  Arch Dis Child       Date:  1974-11       Impact factor: 3.791

Review 3.  Phenylketonuria: a review.

Authors:  J S Yu
Journal:  Postgrad Med J       Date:  1970-07       Impact factor: 2.401

4.  Screening for inherited metabolic disease by plasma chromatography (Scriver) in a large city.

Authors:  D N Raine; J R Cooke; W A Andrews; D F Mahon
Journal:  Br Med J       Date:  1972-07-01

5.  Phenylketonuria. Mass screening of newborns in Ireland.

Authors:  S F Cahalane
Journal:  Arch Dis Child       Date:  1968-04       Impact factor: 3.791

6.  Phenylketonuria. Early detection, diagnosis and treatment.

Authors:  G C Cunningham
Journal:  Calif Med       Date:  1966-07

7.  Compound heterozygosity in nonphenylketonuria hyperphenylalanemia: the contribution of mutations for classical phenylketonuria.

Authors:  S Avigad; S Kleiman; M Weinstein; B E Cohen; G Schwartz; S L Woo; Y Shiloh
Journal:  Am J Hum Genet       Date:  1991-08       Impact factor: 11.025

  7 in total

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