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 *

112 related articles for article (PubMed ID: 14576578)

  • 1. [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]  

  • 2. HFE gene mutations are extremely rare in Western sub-Saharan Africa.
    Martins R; Picanço I; Nunes B; Romão L; Faustino P
    Ann Hematol; 2005 Oct; 84(10):686-8. PubMed ID: 15834568
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. [Arthropathy of hereditary hemochromatosis].
    Rihl M; Kellner H
    Z Rheumatol; 2004 Feb; 63(1):22-9. PubMed ID: 14991275
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Haemochromatosis and HLA-H.
    Jouanolle AM; Gandon G; Jézéquel P; Blayau M; Campion ML; Yaouanq J; Mosser J; Fergelot P; Chauvel B; Bouric P; Carn G; Andrieux N; Gicquel I; Le Gall JY; David V
    Nat Genet; 1996 Nov; 14(3):251-2. PubMed ID: 8896550
    [No Abstract]   [Full Text] [Related]  

  • 6. Population genetic screening for hereditary haemochromatosis: are we a step closer?
    Allen KJ
    Med J Aust; 2008 Sep; 189(6):300-1. PubMed ID: 18803529
    [No Abstract]   [Full Text] [Related]  

  • 7. Haemochromatosis: pathological or beneficial.
    Worwood M
    Schweiz Med Wochenschr; 1998 Dec; 128(49):1925-35. PubMed ID: 9887470
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Hereditary hemochromatosis: biochemical and genetic diagnosis].
    Quintero E
    Gastroenterol Hepatol; 1999 Feb; 22 Suppl 1():1-5. PubMed ID: 10085593
    [No Abstract]   [Full Text] [Related]  

  • 9. [Hemochromatosis, a public health problem].
    Aguilar Martinez P
    Soins; 2007 Jun; (716):34-5. PubMed ID: 17718029
    [No Abstract]   [Full Text] [Related]  

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

  • 11. Hereditary haemochromatosis.
    Janssen MC; Swinkels DW
    Best Pract Res Clin Gastroenterol; 2009; 23(2):171-83. PubMed ID: 19414144
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genotype-phenotype correlation in a Spanish population homozygous for the H63D mutation of the HFE gene.
    Remacha AF; Sardà MP; Barceló MJ; Bach V; Altès A; Baiget M; Guarner C; Blesa I
    Ann Hematol; 2006 May; 85(5):340-2. PubMed ID: 16523311
    [No Abstract]   [Full Text] [Related]  

  • 13. The importance of screening for hemochromatosis.
    Dubois S; Kowdley KV
    Arch Intern Med; 2003 Nov; 163(20):2424-6; author reply 2426. PubMed ID: 14609776
    [No Abstract]   [Full Text] [Related]  

  • 14. [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]  

  • 15. 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]  

  • 16. 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]  

  • 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. The geography of HFE mutations: molecular diagnosis of haemochromatosis and the globalization of genetic testing.
    Salto-Tellez M; Siew-Chuan Koay E
    Eur J Hum Genet; 2004 Nov; 12(11):877-8. PubMed ID: 15340365
    [No Abstract]   [Full Text] [Related]  

  • 19. Hemochromatosis: a genetic defect in iron metabolism.
    Jazwinska EC
    Bioessays; 1998 Jul; 20(7):562-8. PubMed ID: 9723005
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Lessons from a survey of genotyping for hereditary haemochromatosis.
    Francis S; Thachil J
    J Clin Pathol; 2015 Jul; 68(7):578. PubMed ID: 25935547
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.