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 *

143 related articles for article (PubMed ID: 10673284)

  • 1. Population screening for haemochromatosis.
    Adams PC
    Gut; 2000 Mar; 46(3):301-3. PubMed ID: 10673284
    [No Abstract]   [Full Text] [Related]  

  • 2. Hereditary haemochromatosis: never seen a case?
    Emery J; Rose P
    Br J Gen Pract; 2001 May; 51(466):347-8. PubMed ID: 11360695
    [No Abstract]   [Full Text] [Related]  

  • 3. Population screening for hemochromatosis.
    Adams PC
    Hepatology; 1999 Apr; 29(4):1324-7. PubMed ID: 10094982
    [No Abstract]   [Full Text] [Related]  

  • 4. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis Consortium.
    Merryweather-Clarke AT; Pointon JJ; Shearman JD; Robson KJ; Jouanolle AM; Mosser A; David V; Le Gall JY; Halsall DJ; Elsey TS; Kelly A; Cox TM; Clare M; Bomford A; Vandwalle JL; Rochette J; Borot N; Coppin H; Roth MP; Ryan E; Crowe J; Totaro A; Gasparini P; Roetto A; Walker AP
    Nat Genet; 1999 Nov; 23(3):271. PubMed ID: 10545942
    [No Abstract]   [Full Text] [Related]  

  • 5. [Hemochromatosis].
    Moirand R
    Gastroenterol Clin Biol; 2000 May; 24(5 Pt 2):B68-78. PubMed ID: 10891767
    [No Abstract]   [Full Text] [Related]  

  • 6. [Genetic screening of hemochromatosis].
    Brissot P
    Rev Med Interne; 1998 Mar; 19(3):165-7. PubMed ID: 9775135
    [No Abstract]   [Full Text] [Related]  

  • 7. Best practice guidelines for the molecular genetic diagnosis of Type 1 (HFE-related) hereditary haemochromatosis.
    King C; Barton DE
    BMC Med Genet; 2006 Nov; 7():81. PubMed ID: 17134494
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Patient-focused outcomes following detection in a hospital-based screening programme for C282Y haemochromatosis.
    McCullen MA; Fletcher LM; Dimeski G; Pink A; Powell LW; Crawford DH; Hickman PE
    Intern Med J; 2008 Aug; 38(8):651-6. PubMed ID: 18284459
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Should one screen systematically for genetic haemochromatosis?].
    Le Gall JY
    Presse Med; 2003 Oct; 32(34):1588-90. PubMed ID: 14576578
    [No Abstract]   [Full Text] [Related]  

  • 10. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
    Noll WW; Belloni DR; Stenzel TT; Grody WW
    Nat Genet; 1999 Nov; 23(3):271-2. PubMed ID: 10610176
    [No Abstract]   [Full Text] [Related]  

  • 11. What is the role of genetic testing in diagnosis of haemochromatosis?
    Worwood M
    Ann Clin Biochem; 2001 Jan; 38(Pt 1):3-19. PubMed ID: 11270839
    [No Abstract]   [Full Text] [Related]  

  • 12. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
    Gomez PS; Parks S; Ries R; Tran TC; Gomez PF; Press RD
    Nat Genet; 1999 Nov; 23(3):272. PubMed ID: 10545944
    [No Abstract]   [Full Text] [Related]  

  • 13. Detecting genetic haemochromatosis.
    Dooley JS; Walker AP
    Practitioner; 2007 May; 251(1694):82, 84, 86 passim. PubMed ID: 17564138
    [No Abstract]   [Full Text] [Related]  

  • 14. Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?
    Cadet E; Capron D; Gallet M; Omanga-Léké ML; Boutignon H; Julier C; Robson KJ; Rochette J
    J Med Genet; 2005 May; 42(5):390-5. PubMed ID: 15863667
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Screening for hereditary haemochromatosis within families and beyond.
    McCune CA; Ravine D; Worwood M; Jackson HA; Evans HM; Hutton D
    Lancet; 2003 Dec; 362(9399):1897-8. PubMed ID: 14667749
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Review article: targeted screening for hereditary haemochromatosis in high-risk groups.
    DuBois S; Kowdley KV
    Aliment Pharmacol Ther; 2004 Jul; 20(1):1-14. PubMed ID: 15225165
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Early detection of genetic hemochromatosis: should all young adults be offered the genetic test?
    Worwood M
    Genet Test; 2000; 4(2):219-28. PubMed ID: 10953963
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Frequency of HFE gene mutations and genotype-phenotype correlations in patients with hereditary hemochromatosis in Switzerland].
    Himmelmann A; Bortoluzzi L; Jansen S; Fehr J
    Schweiz Med Wochenschr; 2000 Aug; 130(31-32):1112-9. PubMed ID: 11008304
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Haemochromatosis and family testing. What should a GP do?
    Newstead J; Delatycki M; Aitken MA
    Aust Fam Physician; 2002 Jun; 31(6):533-7. PubMed ID: 12154600
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Automated measurement of unsaturated iron binding capacity is an effective screening strategy for C282Y homozygous haemochromatosis.
    Hickman PE; Hourigan LF; Powell LW; Cordingley F; Dimeski G; Ormiston B; Shaw J; Ferguson W; Johnson M; Ascough J; McDonell K; Pink A; Crawford DH
    Gut; 2000 Mar; 46(3):405-9. PubMed ID: 10673305
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.