These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

154 related articles for article (PubMed ID: 9462195)

  • 1. Audit of neonatal screening programme for phenylketonuria and congenital hypothyroidism.
    Simpson N; Randall R; Lenton S; Walker S
    Arch Dis Child Fetal Neonatal Ed; 1997 Nov; 77(3):F228-34. PubMed ID: 9462195
    [TBL] [Abstract][Full Text] [Related]  

  • 2. An audit of the organisation of neonatal screening for phenylketonuria and congenital hypothyroidism in the Northern Region.
    Galloway A; Stevenson J
    Public Health; 1996 Mar; 110(2):119-21. PubMed ID: 8901256
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Audit improves neonatal (Guthrie) screening programme.
    Galloway A; Stevenson J
    BMJ; 1994 Oct; 309(6958):878. PubMed ID: 7848435
    [No Abstract]   [Full Text] [Related]  

  • 4. [Screening of newborn infants in Norway for severe metabolic disease].
    Pettersen RD; Saugstad OD; Heyerdahl S; Motzfeldt K; Lie SO
    Tidsskr Nor Laegeforen; 1995 Feb; 115(5):584-7. PubMed ID: 7900109
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Examination of newborn infants in the first week. Techniques and objectives including early and systematic screening of congenital hypothyroidism and phenylketonuria].
    Lequien P
    Rev Prat; 1991 Feb; 41(4):357-60. PubMed ID: 2008589
    [No Abstract]   [Full Text] [Related]  

  • 6. Neonatal screening: current trends and quality control in the United Kingdom.
    Green A
    Rinsho Byori; 1998 Mar; 46(3):211-6. PubMed ID: 9564759
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Neonatal screening for metabolic diseases--a task without priority in the Norwegian health policy?].
    Pettersen RD; Saugstad OD; Lie SO
    Tidsskr Nor Laegeforen; 1995 Feb; 115(5):607-8. PubMed ID: 7900116
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [A cost-benefit evaluation of neonatal screening for phenylketonuria and congenital hypothyroidism].
    Gu X; Wang J; Ye J; Cheng X
    Zhonghua Yu Fang Yi Xue Za Zhi; 2000 May; 34(3):147-9. PubMed ID: 11860921
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. [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; 53(4):446-52. PubMed ID: 19649383
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Performance of neonatal screening programme must be monitored.
    Galloway A; Stevenson J
    BMJ; 1996 May; 312(7039):1158. PubMed ID: 8620148
    [No Abstract]   [Full Text] [Related]  

  • 12. [Cost/benefit study of the neonatal detection of phenylketonuria and hypothyroidism].
    Dhondt JL; Farriaux JP; Lebrun T; Sailly JC
    Pediatrie; 1988; 43(4):345-8. PubMed ID: 3138627
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 76(5):411-5. PubMed ID: 9196355
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The implementation of revised guidelines and the performance of a screening programme for congenital hypothyroidism.
    Korada M; Kibirige M; Turner S; Day J; Johnstone H; Cheetham T
    J Med Screen; 2008; 15(1):5-8. PubMed ID: 18416947
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Improvements to the newborn bloodspot screening service are required to meet national standards.
    Bello S; Ferguson C; Wallis R
    J Med Screen; 2010; 17(3):114-20. PubMed ID: 20956720
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Audit of newborn screening programme for congenital hypothyroidism.
    Zarina AL; Rahmah R; Bador KM; Ng SF; Wu LL
    Med J Malaysia; 2008 Oct; 63(4):325-8. PubMed ID: 19385494
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neonatal screening of phenylketonuria and congenital hypothyroidism in China.
    Fan GX; Jun Y; Rui-guan C
    Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():17-9. PubMed ID: 11400761
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Screening for phenylketonuria and congenital hypothyroidism in 5.8 million neonates in China].
    Gu XF; Wang ZG
    Zhonghua Yu Fang Yi Xue Za Zhi; 2004 Mar; 38(2):99-102. PubMed ID: 15061917
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Neonatal screening for phenylketonuria and hypothyroidism. An optimizing system].
    Reviron D; Auquier P; Giusiano B; Maurin N; Sambuc R; Giraud F
    Arch Fr Pediatr; 1990 Apr; 47(4):255-6. PubMed ID: 2363612
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Evaluation of the detection of phenylketonuria and hypothyroidism at the Lille Regional Center].
    Dhondt JL; Farriaux JP; Raux M; Paux E; Bouchery AM; Debersée J
    Arch Fr Pediatr; 1987 Nov; 44(9):787-90. PubMed ID: 3446070
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.