Literature DB >> 14484110

Variations in intelligence in phenylktonuria.

M W PARTINGTON.   

Abstract

Keywords:  INTELLIGENCE TESTS; PHENYLPYRUVIC OLIGOPHRENIA/psychology

Mesh:

Year:  1962        PMID: 14484110      PMCID: PMC1849025     

Source DB:  PubMed          Journal:  Can Med Assoc J        ISSN: 0008-4409            Impact factor:   8.262


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  16 in total

1.  Phenylketonuria with normal intelligence.

Authors:  R J ALLEN; R M GIBSON
Journal:  Am J Dis Child       Date:  1961-07

2.  A case of phenylketonuria in the Eta resulting from the mating of a homozygous father and a heterozygous mother.

Authors:  N FUJIKI; A L DREW; M MIYAKE; H NEMOTO; C SUJAKU; T SHIMADA
Journal:  Am J Hum Genet       Date:  1961-03       Impact factor: 11.025

3.  The early symptoms of phenylketonuria.

Authors:  M W PARTINGTON
Journal:  Pediatrics       Date:  1961-03       Impact factor: 7.124

4.  Phenylketonuria treated from earliest infancy; report of three cases.

Authors:  F A HORNER; C W STREAMER
Journal:  AMA J Dis Child       Date:  1959-03

5.  An evaluation of the treatment of phenylketonuria with diets low in phenylalanine.

Authors:  W E KNOX
Journal:  Pediatrics       Date:  1960-07       Impact factor: 7.124

6.  Pathogenetic problems in phenylketonuria.

Authors:  W E KNOX; D Y HSIA
Journal:  Am J Med       Date:  1957-05       Impact factor: 4.965

7.  Phenylketonuria with normal intelligence and Gowers' muscular dystrophy.

Authors:  S COATES; A P NORMAN; L I WOOLF
Journal:  Arch Dis Child       Date:  1957-08       Impact factor: 3.791

8.  Phenylketonuria: the phenylalanine-tyrosine ratio in the detection of the heterozygous carrier.

Authors:  D Y Y HSIA
Journal:  J Ment Defic Res       Date:  1958-06

9.  Studies on phenylketonuria. V. Observations on a newborn infant with phenylketonuria.

Authors:  M D ARMSTRONG; E L BINKLEY
Journal:  Proc Soc Exp Biol Med       Date:  1956-12

10.  Phenylketonuria. II. Results of treatment of infants and young children. A report of 10 cases.

Authors:  W R CENTERWALL; S A CENTERWALL; V ARMON; L B MANN
Journal:  J Pediatr       Date:  1961-07       Impact factor: 4.406

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  10 in total

1.  CASE-FINDING IN PHENYLKETONURIA. I. REPORT OF A SURVEY BY THE COLLEGE OF GENERAL PRACTICE OF CANADA.

Authors:  M W PARTINGTON; R M ANDERSON
Journal:  Can Med Assoc J       Date:  1964-06-06       Impact factor: 8.262

2.  CASE FINDING IN PHENYLKETONURIA. II. THE GUTHRIE TEST.

Authors:  M W PARTINGTON; B SINNOTT
Journal:  Can Med Assoc J       Date:  1964-07-18       Impact factor: 8.262

Review 3.  Undiagnosed phenylketonuria in adult women: a hidden public health problem.

Authors:  W B Hanley; J T Clarke; W E Schoonheyt
Journal:  CMAJ       Date:  1990-09-15       Impact factor: 8.262

Review 4.  Phenylketonuria and its variations. A review of recent developments.

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

5.  Phenylketonuria in New York State.

Authors:  S Kelly; J Palombi
Journal:  Public Health Rep       Date:  1967-10       Impact factor: 2.792

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

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

7.  Phenylketonuria. Mass screening of newborns in Ireland.

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

8.  Maternal Phenylketonuria Collaborative Study (MPKUCS)--the 'outliers'.

Authors:  W B Hanley; C Azen; R Koch; K Michals-Matalon; R Matalon; B Rouse; F Trefz; S Waisbren; F de la Cruz
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

Review 9.  Diseases of phenylalanine metabolism.

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

10.  Polysome immunoprecipitation of phenylalanine hydroxylase mRNA from rat liver and cloning of its cDNA.

Authors:  K J Robson; T Chandra; R T MacGillivray; S L Woo
Journal:  Proc Natl Acad Sci U S A       Date:  1982-08       Impact factor: 11.205

  10 in total

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