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 *

103 related articles for article (PubMed ID: 14576578)

  • 21. Testing families with HFE-related hereditary haemochromatosis.
    Siezenga MA; Rasp E; Wijermans PW
    Neth J Med; 2004 May; 62(5):156-9. PubMed ID: 15366698
    [TBL] [Abstract][Full Text] [Related]  

  • 22. What is HFE haemochromatosis?
    Marjot T; Collier J; Ryan JD
    Br J Hosp Med (Lond); 2016 Jun; 77(6):C91-5. PubMed ID: 27269766
    [No Abstract]   [Full Text] [Related]  

  • 23. 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]  

  • 24. Review article: the modern diagnosis and management of haemochromatosis.
    Adams PC
    Aliment Pharmacol Ther; 2006 Jun; 23(12):1681-91. PubMed ID: 16817911
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Clinical usefulness of the detection of mutations of the HFE gene in hemochromatosis].
    Oliva R; Sánchez M; Bruguera M; Rodés J
    Gastroenterol Hepatol; 2000 Nov; 23(9):433-5. PubMed ID: 11126040
    [No Abstract]   [Full Text] [Related]  

  • 26. [Diagnosis and treatment of genetic haemochromatosis].
    Milman NT
    Ugeskr Laeger; 2013 Apr; 175(16):1109-12. PubMed ID: 23651749
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prevalence of C282Y, H63D and S65C mutations of the hemochromatosis (HFE) gene in a population from southeastern Spain (Murcia Region).
    Muro M; Moya-Quiles MR; Botella C; Alvarez-López MR
    Clin Genet; 2007 Jan; 71(1):97-8. PubMed ID: 17204056
    [No Abstract]   [Full Text] [Related]  

  • 28. Frequency of hemochromatosis gene (HFE) mutations in Corsica (France).
    Piras I; Melis A; Falchi A; Varesi L; Calò CM; Vona G
    Clin Genet; 2007 Sep; 72(3):268-70. PubMed ID: 17718867
    [No Abstract]   [Full Text] [Related]  

  • 29. Haemochromatosis... definite maybe!
    Nat Genet; 1996 Aug; 13(4):375-6. PubMed ID: 8696321
    [No Abstract]   [Full Text] [Related]  

  • 30. 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]  

  • 31. Transferrin saturation phenotype and HFE genotype screening for hemochromatosis and primary iron overload: predictions from a model based on national, racial, and ethnic group composition in central Alabama.
    Barton JC; Acton RT
    Genet Test; 2000; 4(2):199-206. PubMed ID: 10953960
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Homozygous G320V mutation in the HJV gene causing juvenile hereditary haemochromatosis type A. A case report.
    Militaru MS; Popp RA; Trifa AP
    J Gastrointestin Liver Dis; 2010 Jun; 19(2):191-3. PubMed ID: 20593054
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Transferrin saturation should not be corrected for body mass index in screening studies for haemochromatosis.
    Thorstensen K; Asberg A
    J Hepatol; 2006 May; 44(5):1003-4. PubMed ID: 16551484
    [No Abstract]   [Full Text] [Related]  

  • 34. Prevalence of HFE (hemochromatosis) gene mutations C282Y and H63D in a Romanian population.
    Voicu PM; Cojocariu C; Petrescu-Danila E; Covic M; Stanciu C; Rusu M
    Blood Cells Mol Dis; 2009; 42(1):14-5. PubMed ID: 18842428
    [No Abstract]   [Full Text] [Related]  

  • 35. [Hemochromatosis].
    Lefrère F
    Rev Prat; 2007 Dec; 57(20):2291-6. PubMed ID: 18320752
    [No Abstract]   [Full Text] [Related]  

  • 36. Prevalence of H63D, S65C and C282Y mutations of the HFE gene in 1120 voluntary blood donors from Antioquia region of northwest Colombia.
    Avila-Gomez IC; Aristizabal-Bernal B; Jimenez-Del-Rio M; Velez-Pardo C
    Blood Cells Mol Dis; 2008; 40(3):449-51. PubMed ID: 18289891
    [No Abstract]   [Full Text] [Related]  

  • 37. Hereditary hemochromatosis: detection of C282Y and H63D mutations in HFE gene by means of guthrie cards in population of Czech Republic.
    Cimburova M; Putova I; Provaznikova H; Horak J
    Genet Epidemiol; 2002 Oct; 23(3):260-3. PubMed ID: 12384978
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Hereditary hemochromatosis--new developments after discovery of the HFE gene].
    Erhardt A; Niederau C; Osman Y; Häussinger D
    Z Gastroenterol; 1999 Dec; 37(12):1179-85. PubMed ID: 10666843
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Hemochromatosis case definition: out of focus?
    Adams PC
    Nat Clin Pract Gastroenterol Hepatol; 2006 Apr; 3(4):178-9. PubMed ID: 16582939
    [No Abstract]   [Full Text] [Related]  

  • 40. Hereditary iron overload: update on pathophysiology, diagnosis, and treatment.
    Franchini M
    Am J Hematol; 2006 Mar; 81(3):202-9. PubMed ID: 16493621
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.