BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 7207294)

  • 1. Genetic screening of newborn in Australia: results for 1979.
    Pitt D; Connelly J; Francis I; Wilcken B; Brown DA; Robertson E; Hill G; Masters P; Tucker RG; Raby J; McFarlane J; Hancock J
    Med J Aust; 1981 Jan; 1(1):39-40. PubMed ID: 7207294
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic screening of newborn in Australia. Results for 1981.
    Pitt D; Connelly J; Francis I; Wilcken B; Brown DA; Robertson E; Hill G; Masters P; Raby J; McFarlane J; Bowling F; Hancock J
    Med J Aust; 1983 Apr; 1(7):333-5. PubMed ID: 6835136
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic screening of newborn in Australia: results for 1980.
    Pitt D; Connelly J; Francis I; Wilcken B; Brown DA; Robertson E; Hill G; Masters P; Tucker RG; Raby J; McFarlane J; Hancock J
    Med J Aust; 1982 Feb; 1(3):119-20. PubMed ID: 7132849
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic screening of the newborn in Australia. Results for 1978.
    Pitt D; Connelly J; Francis I; Wilcken B; Brown DA; Hill G; Masters P; Tucker RG; Raby J; McFarlane J
    Med J Aust; 1979 Sep; 2(5):272-3. PubMed ID: 514173
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Newborn phenylalanine/tyrosine metabolism. Implications for screening for phenylketonuria.
    Schneider AJ
    Am J Dis Child; 1983 May; 137(5):427-32. PubMed ID: 6846269
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Newborn phenylketonuria (PKU) Guthrie (BIA) screening and early hospital discharge.
    Hanley WB; Demshar H; Preston MA; Borczyk A; Schoonheyt WE; Clarke JT; Feigenbaum A
    Early Hum Dev; 1997 Jan; 47(1):87-96. PubMed ID: 9118832
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Newborn screening for metabolic disorders in Australia and New Zealand: results for 1983. Human Genetics Society of Australasia Newborn Screening Committee.
    Med J Aust; 1985 Aug; 143(4):159-60. PubMed ID: 4021909
    [No Abstract]   [Full Text] [Related]  

  • 8. Non-phenylketonuria hyperphenylalaninaemia in Northern Ireland: frequent mutation allows screening and early diagnosis.
    Zschocke J; Graham CA; Stewart FJ; Carson DJ; Nevin NC
    Hum Mutat; 1994; 4(2):114-8. PubMed ID: 7981714
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Extremely high phenylalanine levels in a newborn on parenteral nutrition: phenylketonuria in the neonatal intensive care unit.
    Lin HJ; Kwong AM; Carter JM; Ferreira BF; Austin MF; Devarajan K; Coleman RJ; Feuchtbaum LB; Lorey F; Jonas AJ
    J Perinatol; 2011 Jul; 31(7):507-10. PubMed ID: 21712831
    [TBL] [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; 66(1-2):11-3. PubMed ID: 19485249
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Evaluation of 6-year application of the enzymatic colorimetric phenylalanine assay in the setting of neonatal screening for phenylketonuria.
    Schulze A; Mayatepek E; Hoffmann GF
    Clin Chim Acta; 2002 Mar; 317(1-2):27-37. PubMed ID: 11814455
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Follow-up study of 16 years neonatal screening for inborn errors of metabolism in West Germany.
    Mathias D; Bickel H
    Eur J Pediatr; 1986 Sep; 145(4):310-2. PubMed ID: 3770001
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Neonatal screening for congenital hypothyroidism and phenylketonuria].
    Velázquez A; Loera-Luna A; Aguirre BE; Gamboa S; Vargas H; Robles C
    Salud Publica Mex; 1994; 36(3):249-56. PubMed ID: 7940004
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [15 years of national screening for phenylketonuria in The Netherlands; 4th Report of the National Commission for Management of Phenylketonuria].
    Verkerk PH; Vaandrager GJ; Sengers RC
    Ned Tijdschr Geneeskd; 1990 Dec; 134(52):2533-6. PubMed ID: 2270129
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Program of neonatal screening for phenylketonuria].
    Cornejo V; Raimann E; Moraga M; Colombo M
    Rev Chil Pediatr; 1990; 61(6):309-12. PubMed ID: 2152214
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Screening for phenylketonuria in 726,998 neonates in Zhejiang Province].
    Zhao ZY; Qu YP; Qu LQ; Yu XL
    Zhejiang Da Xue Xue Bao Yi Xue Ban; 2005 Mar; 34(2):185-7. PubMed ID: 15812897
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Experience based on 800,000 newborn screening tests of the Budapest Phenylketonuria Centre.
    Szabó L; Somogyi C; Máté M
    Acta Paediatr Hung; 1985; 26(2):113-25. PubMed ID: 4041279
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Health economic analysis of the Swedish neonatal metabolic screening programme. A method of optimizing routines.
    Alm J; Larsson A; Rosenqvist U
    Med Decis Making; 1982; 2(1):33-45. PubMed ID: 6820461
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of the "report on a cooperative study of various fluorometric procedures and the Guthrie Bacterial Inhibition Assay in the determination of hyperphenylalaninemia" and the significance of this study in the detection, diagnosis, and management of phenylketonuria (PKU).
    Ambrose JA
    Health Lab Sci; 1973 Jul; 10(3):188-94. PubMed ID: 4720477
    [No Abstract]   [Full Text] [Related]  

  • 20. [Evaluation of the usefulness for neonatal mass screening in light of 35 years personal experience].
    Bozkowa K; Cabalska B; Radomyska B; Ołtarzewski M; Lenartowska I
    Med Wieku Rozwoj; 1999; 3(4):529-59. PubMed ID: 10910678
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.