Literature DB >> 6015901

Hyperphenylalanemia without phenylketonuria.

M E O'Flynn, P Tillman, D Y Hsia.   

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Year:  1967        PMID： 6015901     DOI： 10.1001/archpedi.1967.02090160072005

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN： 0002-922X


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  6 in total

1.  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

2.  [A case of "classical" phenylketonuria with average intelligence].

Authors:  W Schwenke; A Anke; A Knapp
Journal:  Klin Wochenschr       Date:  1969-10-01

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

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

4.  Biopterin defect in a normal-appearing child affected by a transient phenylketonuria.

Authors:  F Rey; R J Leeming; J A Blair; J Rey
Journal:  Arch Dis Child       Date:  1980-08       Impact factor: 3.791

Review 5.  Diseases of phenylalanine metabolism.

Authors:  C E Parker
Journal:  West J Med       Date:  1979-10

6.  Phenylketonuria and its variants: observations on intellectual functioning.

Authors:  C Netley; W B Hanley; H L Rudner
Journal:  Can Med Assoc J       Date:  1984-10-01       Impact factor: 8.262
  6 in total

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