Literature DB >> 4773479

Classic phenylketonuria: heterozygote detection during pregnancy.

R F Griffin, M E Humienny, E C Hall, L J Elsas.   

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Year:  1973        PMID： 4773479      PMCID： PMC1762571     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  14 in total

1.  A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS.

Authors:  R GUTHRIE; A SUSI
Journal:  Pediatrics       Date:  1963-09       Impact factor: 7.124

2.  The detection in the heterozygote of the metabolic effect of the recessive gene for phenylketonuria.

Authors:  W E KNOX; E C MESSINGER
Journal:  Am J Hum Genet       Date:  1958-03       Impact factor: 11.025

3.  MENDELIAN PROPORTIONS IN A MIXED POPULATION.

Authors:  G H Hardy
Journal:  Science       Date:  1908-07-10       Impact factor: 47.728

4.  Problems in the biochemical detection of heterozygotes for phenylketonuria.

Authors:  L Y Yakymyshyn; D W Reid; D J Campbell
Journal:  Clin Biochem       Date:  1972-03       Impact factor: 3.281

5.  Detection of phenylketonuric heterozygotes.

Authors:  S H Jackson; W B Hanley; T Gero; G D Gosse
Journal:  Clin Chem       Date:  1971-06       Impact factor: 8.327

6.  Familial iminoglycinuria. An inborn error of renal tubular transport.

Authors:  L E Rosenberg; J L Durant; L J Elsas
Journal:  N Engl J Med       Date:  1968-06-27       Impact factor: 91.245

7.  Heterogeneity in genetic control of phenylalanine metabolism in man.

Authors:  D Rosenblatt; C R Scriver
Journal:  Nature       Date:  1968-05-18       Impact factor: 49.962

8.  Free amino-acid concentrations in fetal fluids.

Authors:  F Cockburn; S P Robins; J O Forfar
Journal:  Br Med J       Date:  1970-09-26

9.  Determination of heterozygosity for phenylketonuria on the amino acid analyzer.

Authors:  T L Perry; S Hansen; B Tischler; R Bunting
Journal:  Clin Chim Acta       Date:  1967-10       Impact factor: 3.786

10.  Phenylalanine tolerance tests. In families with phenylketonuria and hyperphenylalaninemia.

Authors:  G C Cunningham; R W Day; J L Berman; D Y Hsia
Journal:  Am J Dis Child       Date:  1969-06
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  5 in total

1.  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

2.  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

3.  Diet, genetics, and mental retardation interaction between phenylketonuric heterozygous mother and fetus to produce nonspecific diminution of IQ: evidence in support of the justification hypothesis.

Authors:  S P Bessman; M L Williamson; R Koch
Journal:  Proc Natl Acad Sci U S A       Date:  1978-03       Impact factor: 11.205

4.  Cord-blood tyrosine levels in the full-term phenylketonuric fetus and the "justification hypothesis".

Authors:  C R Scriver; D E Cole; S A Houghton; H L Levy; A Grenier; C Laberge
Journal:  Proc Natl Acad Sci U S A       Date:  1980-10       Impact factor: 11.205

5.  Gender dimorphism in aspartame-induced impairment of spatial cognition and insulin sensitivity.

Authors:  Kate S Collison; Nadine J Makhoul; Marya Z Zaidi; Soad M Saleh; Bernard Andres; Angela Inglis; Rana Al-Rabiah; Futwan A Al-Mohanna
Journal:  PLoS One       Date:  2012-04-03       Impact factor: 3.240
  5 in total

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