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Journal Abstract Search

161 related items for PubMed ID: 1912773

  • 1. Review of neonatal screening programme for phenylketonuria.
    Smith I, Cook B, Beasley M.
    BMJ; 1991 Aug 10; 303(6798):333-5. PubMed ID: 1912773
    [Abstract] [Full Text] [Related]

  • 2. Routine neonatal screening for phenylketonuria in the United Kingdom 1964-78. Medical Research Council Steering Committee for the MRC/DHSS Phenylketonuria Register.
    Br Med J (Clin Res Ed); 1981 May 23; 282(6277):1680-4. PubMed ID: 6786433
    [Abstract] [Full Text] [Related]

  • 3. [Evaluation of the Neonatal Screening Program for congenital hypothyroidism and phenylketonuria in the State of Mato Grosso, Brazil].
    Stranieri I, Takano OA.
    Arq Bras Endocrinol Metabol; 2009 Jun 23; 53(4):446-52. PubMed ID: 19649383
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  • 5. [Neonatal screening program at the university hospital of the Ribeirão Preto School of Medicine, São Paulo University, Brazil].
    Magalhães PK, Turcato Mde F, Angulo Ide L, Maciel LM.
    Cad Saude Publica; 2009 Feb 23; 25(2):445-54. PubMed ID: 19219252
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  • 6. Phenylketonuria screening in the Republic of Macedonia.
    Kocova M, Anastasovska V.
    Orphanet J Rare Dis; 2016 Aug 05; 11(1):112. PubMed ID: 27496147
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  • 8. Development of the phenylketonuria screening programme in Estonia.
    Ounap K, Lilleväli H, Metspalu A, Lipping-Sitska M.
    J Med Screen; 1998 Aug 05; 5(1):22-3. PubMed ID: 9575455
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  • 10. Review of neonatal screening programme for phenylketonuria.
    Elliman D, Garner J.
    BMJ; 1991 Aug 24; 303(6800):471. PubMed ID: 1912849
    [No Abstract] [Full Text] [Related]

  • 11. Adverse medical outcomes of early newborn screening programs for phenylketonuria.
    Brosco JP, Sanders LM, Seider MI, Dunn AC.
    Pediatrics; 2008 Jul 24; 122(1):192-7. PubMed ID: 18596006
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  • 12. [Evolution of the neonatal screening program in the state of Tocantins].
    Mendes LC, Santos TT, Bringel Fde A.
    Arq Bras Endocrinol Metabol; 2013 Mar 24; 57(2):112-9. PubMed ID: 23525288
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  • 13. Neonatal screening of phenylketonuria and congenital hypothyroidism in China.
    Fan GX, Jun Y, Rui-guan C.
    Southeast Asian J Trop Med Public Health; 1999 Mar 24; 30 Suppl 2():17-9. PubMed ID: 11400761
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  • 14. Neonatal screening for inborn errors of metabolism: cost, yield and outcome.
    Pollitt RJ, Green A, McCabe CJ, Booth A, Cooper NJ, Leonard JV, Nicholl J, Nicholson P, Tunaley JR, Virdi NK.
    Health Technol Assess; 1997 Mar 24; 1(7):i-iv, 1-202. PubMed ID: 9483160
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  • 15. [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 Mar 24; 66(1-2):11-3. PubMed ID: 19485249
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  • 17. Audit of screening programme for congenital hypothyroidism in Scotland 1979-93.
    Ray M, Muir TM, Murray GD, Kennedy R, Girdwood RW, Donaldson MD.
    Arch Dis Child; 1997 May 24; 76(5):411-5. PubMed ID: 9196355
    [Abstract] [Full Text] [Related]

  • 18. Neonatal screening programme for phenylketonuria.
    BMJ; 1991 Sep 21; 303(6804):716. PubMed ID: 1781843
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