Literature DB >> 5565469

Classical and mild phenylketonuria in a family.

N A Coutts, W M Fyfe.   

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Year:  1971        PMID: 5565469      PMCID: PMC1647771          DOI: 10.1136/adc.46.248.550

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


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  6 in total

1.  Phenylalanine-hydroxylase activity in hyperphenylalaninaemia.

Authors:  P Justice; M E O'Flynn; D Y Hsia
Journal:  Lancet       Date:  1967-04-29       Impact factor: 79.321

Review 2.  Phenylalaninemia.

Authors:  G G Carpenter; V H Auerbach; A M DiGeorge
Journal:  Pediatr Clin North Am       Date:  1968-05       Impact factor: 3.278

3.  Atypical phenylketonuria with borderline or normal intelligence.

Authors:  D Y Hsia; M E O'Flynn; J L Berman
Journal:  Am J Dis Child       Date:  1968-08

4.  Causes for high phenylalanine with normal tyrosine in newborn screening programs.

Authors:  J L Berman; G C Cunningham; R W Day; R Ford; D Y Hsia
Journal:  Am J Dis Child       Date:  1969-01

5.  Phenylketonuria: therapeutic problems.

Authors:  P V Tishler
Journal:  Br Med J       Date:  1969-02-22

6.  Diagnosis of phenylketonuria (phenylalanine hydroxylase deficiency, temporary and permanent).

Authors:  J B Stephenson; M S McBean
Journal:  Br Med J       Date:  1967-09-02
  6 in total
  2 in total

1.  [Urinary phenylalanine metabolites in hyperphenylalaninemia (author's transl)].

Authors:  P Koepp
Journal:  Klin Wochenschr       Date:  1976-11-01

2.  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

  2 in total

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