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Journal Abstract Search

340 related items for PubMed ID: 9695246

  • 1. [The clinical and molecular genetic characteristics of phenylketonuria patients in the Republic of Crimea].
    Afanas'eva NA, Bychkova AM, Livshits LA, Bariliak IR.
    Tsitol Genet; 1998; 32(1):8-14. PubMed ID: 9695246
    [Abstract] [Full Text] [Related]

  • 2. [Genetic heterogeneity and approaches to the prenatal diagnosis of phenylketonuria (review)].
    Chestkov VV, Shishkin SS.
    Vopr Med Khim; 1986; 32(4):7-12. PubMed ID: 3020793
    [Abstract] [Full Text] [Related]

  • 3. [Detection of the mutational gene in phenylketonuria and prenatal diagnoses by using single strand conformation polymorphism methods].
    Yang T, Yuan L, Huang S.
    Zhonghua Fu Chan Ke Za Zhi; 1996 Jul; 31(7):401-3. PubMed ID: 9275410
    [Abstract] [Full Text] [Related]

  • 4. Molecular studies and prenatal diagnosis of phenylketonuria in Chinese patients.
    Fan GX, Qing LX, Jun Y, Mei Z.
    Southeast Asian J Trop Med Public Health; 1999 Jul; 30 Suppl 2():63-5. PubMed ID: 11400788
    [Abstract] [Full Text] [Related]

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  • 7. [Genetic diagnosis in classical phenylketonuria].
    Wulff K, Herrmann FH, Wehnert M, Seidlitz G, Schütz M.
    Z Arztl Fortbild (Jena); 1988 Jul; 82(22):1127-31. PubMed ID: 2907835
    [No Abstract] [Full Text] [Related]

  • 8. [Prenatal diagnosis of genetic diseases. Indications, methods, legal and ethic aspects. Neonatal screening of phenylketonuria and hypothyroidism].
    Farriaux JP.
    Rev Prat; 1997 Dec 01; 47(19):2159-68. PubMed ID: 9501609
    [No Abstract] [Full Text] [Related]

  • 9. Maternal phenylketonuria.
    Paprocka J, Jamroz E, Wiktor M, Marszał E.
    Wiad Lek; 2009 Dec 01; 62(1):11-7. PubMed ID: 19817251
    [Abstract] [Full Text] [Related]

  • 10. [Did the change of technique of screening investigations influence on improvement of test credibility in recognizing and differentiating diagnostics of hiperphenylalaninemias?].
    Didycz B, Lemańska D, Słuszniak A.
    Przegl Lek; 2009 Dec 01; 66(1-2):11-3. PubMed ID: 19485249
    [Abstract] [Full Text] [Related]

  • 11. Early blood sampling in neonatal programs for the detection of phenylketonuria.
    Szeinberg A, Cohen BE.
    Padiatr Padol; 1982 Dec 01; 17(2):287-92. PubMed ID: 7099682
    [Abstract] [Full Text] [Related]

  • 12. [Results, problems and consequences of early treatment of phenylketonuria].
    Theile H, Wässer S, Bührdel P, Graustein I.
    Z Gesamte Inn Med; 1989 Jun 01; 44(11):317-20. PubMed ID: 2669387
    [Abstract] [Full Text] [Related]

  • 13. [Prenatal brain damage in maternal, untreated phenylketonuria].
    Peters WH, Lubs H, Machill G, Knapp A, Pietsch P, Wiechert P.
    Zentralbl Gynakol; 1975 Jun 01; 97(15):905-17. PubMed ID: 1189770
    [Abstract] [Full Text] [Related]

  • 14. Phenylalanine tolerance tests. In families with phenylketonuria and hyperphenylalaninemia.
    Cunningham GC, Day RW, Berman JL, Hsia DY.
    Am J Dis Child; 1969 Jun 01; 117(6):626-35. PubMed ID: 5771502
    [No Abstract] [Full Text] [Related]

  • 15. Prenatal diagnosis by minisatellite analysis in Italian families with phenylketonuria.
    Romano V, Dianzani I, Ponzone A, Zammarchi E, Eisensmith R, Ceratto N, Bosco P, Indelicato A.
    Prenat Diagn; 1994 Oct 01; 14(10):959-62. PubMed ID: 7899270
    [Abstract] [Full Text] [Related]

  • 16. Delayed onset of phenylketonuria.
    Weglage J, van Teefelen-Heithoff A, Zschocke J, Zass R, Marquardt T, Koch HG.
    Eur J Pediatr; 1998 Feb 01; 157(2):171. PubMed ID: 9504799
    [No Abstract] [Full Text] [Related]

  • 17. The role of heterozygosity of women with respect to the phenylketonuria gene in the origin of spontaneous abortions and disturbances of intrauterine fetal development.
    Blyumina MG.
    Sov Genet; 1974 May 01; 8(3):385-90. PubMed ID: 4846205
    [No Abstract] [Full Text] [Related]

  • 18. Impact of neonatal protein metabolism and nutrition on screening for phenylketonuria.
    Ponzone A, Spada M, Roasio L, Porta F, Mussa A, Ferraris S.
    J Pediatr Gastroenterol Nutr; 2008 May 01; 46(5):561-9. PubMed ID: 18493213
    [Abstract] [Full Text] [Related]

  • 19. Issues in newborn screening for phenylketonuria.
    Koch RK.
    Am Fam Physician; 1999 Oct 01; 60(5):1462-6. PubMed ID: 10524490
    [Abstract] [Full Text] [Related]

  • 20. Phenylketonuria: an update.
    Cederbaum S.
    Curr Opin Pediatr; 2002 Dec 01; 14(6):702-6. PubMed ID: 12436039
    [Abstract] [Full Text] [Related]

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