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 *

272 related articles for article (PubMed ID: 12952143)

  • 21. Analysis of HFE genes C282Y, H63D, and S65D in patients with hyperferritinemia from northeastern Brazil.
    Leão GD; Freire JM; Cunha Fernandes AL; Moura de Oliveira TM; Leão ND; Gil EA; de Vasconcelos RC; Azevedo JP; de Farias Sales VS; de Araújo Moura Lemos TM; Leão MD; do Nascimento FF; Maciel JF; de Freitas RV; de Souza Paiva A; Cavalcanti GB
    J Clin Lab Anal; 2014 May; 28(3):178-85. PubMed ID: 24395214
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mild iron overload in patients carrying the HFE S65C gene mutation: a retrospective study in patients with suspected iron overload and healthy controls.
    Holmström P; Marmur J; Eggertsen G; Gåfvels M; Stål P
    Gut; 2002 Nov; 51(5):723-30. PubMed ID: 12377814
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The role of HFE mutations on iron metabolism in beta-thalassemia carriers.
    Martins R; Picanço I; Fonseca A; Ferreira L; Rodrigues O; Coelho M; Seixas T; Miranda A; Nunes B; Costa L; Romão L; Faustino P
    J Hum Genet; 2004; 49(12):651-655. PubMed ID: 15538648
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis.
    Milić S; Ristić S; Starčević-Čizmarević N; Brajenović-Milić B; Crnić-Martinović M; Kapović M; Peterlin B; Štimac D
    Med Sci Monit; 2011 Oct; 17(10):CR552-6. PubMed ID: 21959608
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Hereditary hemochromatosis gene (HFE) mutations C282Y, H63D and S65C in patients with idiopathic dilated cardiomyopathy.
    Hannuksela J; Leppilampi M; Peuhkurinen K; Kärkkäinen S; Saastamoinen E; Heliö T; Kaartinen M; Nieminen MS; Nieminen P; Parkkila S
    Eur J Heart Fail; 2005 Jan; 7(1):103-8. PubMed ID: 15642540
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Frequency and biochemical expression of C282Y/H63D hemochromatosis (HFE) gene mutations in the healthy adult population in Italy.
    Cassanelli S; Pignatti E; Montosi G; Garuti C; Mariano M; Campioli D; Carbonieri A; Baldini E; Pietrangelo A
    J Hepatol; 2001 Apr; 34(4):523-8. PubMed ID: 11394651
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Analysis of HFE gene mutations (C282Y, H63D, and S65C) in the Ecuadorian population.
    Leone PE; Giménez P; Collantes JC; Paz-y-Miño C
    Ann Hematol; 2005 Feb; 84(2):103-5. PubMed ID: 15517265
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis.
    Lawless MW; White M; Mankan AK; O'Dwyer MJ; Norris S
    Tissue Antigens; 2007 Oct; 70(4):294-300. PubMed ID: 17767550
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.
    Gottschalk R; Seidl C; Schilling S; Braner A; Seifried E; Hoelzer D; Kaltwasser JP
    Eur J Immunogenet; 2000 Jun; 27(3):129-34. PubMed ID: 10940080
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Screening selected blood donors with biochemical iron overload for hemochromatosis: a regional experience.
    De Gobbi M; D'Antico S; Castagno F; Testa D; Merlini R; Bondi A; Camaschella C
    Haematologica; 2004 Oct; 89(10):1161-7. PubMed ID: 15477198
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis.
    Porto G; Alves H; Rodrigues P; Cabeda JM; Portal C; Ruivo A; Justiça B; Wolff R; De Sousa M
    Immunogenetics; 1998 Apr; 47(5):404-10. PubMed ID: 9510559
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Frequency of the HFE gene mutations in five Italian populations.
    Candore G; Mantovani V; Balistreri CR; Lio D; Colonna-Romano G; Cerreta V; Carru C; Deiana L; Pes G; Menardi G; Perotti L; Miotti V; Bevilacqua E; Amoroso A; Caruso C
    Blood Cells Mol Dis; 2002; 29(3):267-73. PubMed ID: 12547216
    [TBL] [Abstract][Full Text] [Related]  

  • 33. HFE mutations and hemochromatosis in Danish patients admitted for HFE genotyping.
    Koefoed P; Dalhoff K; Dissing J; Kramer I; Milman N; Pedersen P; Simonsen K; Tygstrup N; Nielsen FC
    Scand J Clin Lab Invest; 2002; 62(7):527-35. PubMed ID: 12512743
    [TBL] [Abstract][Full Text] [Related]  

  • 34. HFE mutations, iron deficiency and overload in 10,500 blood donors.
    Jackson HA; Carter K; Darke C; Guttridge MG; Ravine D; Hutton RD; Napier JA; Worwood M
    Br J Haematol; 2001 Aug; 114(2):474-84. PubMed ID: 11529872
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Molecular diagnosis of hereditary hemochromatosis: application of a newly-developed reverse-hybridization assay in the South African population.
    Kotze MJ; de Villiers JN; Bouwens CS; Warnich L; Zaahl MG; van der Merwe S; Oberkanins C
    Clin Genet; 2004 Apr; 65(4):317-21. PubMed ID: 15025725
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Frequencies of C282Y and H63D mutations and transferrin saturation indices in the Korean population.
    Choi SJ; Min WK; Chun S; Park H; Kim JW; Park CJ; Chi HS
    Clin Chem Lab Med; 2002 Jul; 40(7):689-92. PubMed ID: 12241015
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Frequency of the hemochromatosis gene (HFE) variants in a Jordanian Arab population and in diabetics from the same region.
    Alkhateeb A; Uzrail A; Bodoor K
    Dis Markers; 2009; 27(1):17-22. PubMed ID: 19822954
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. [Mutations in the HFE gene (C282Y, H63D, S65C) in alcoholic patients with finding of iron overload].
    Campos Franco J; González Quintela A; Fernández de Trocóniz LL; Barros Angueira F; Pérez-Quintela BV; Pérez Becerra E; Martínez de Rituerto ST; Otero Antón E; Torre Carballada JA
    Rev Clin Esp; 2002 Oct; 202(10):534-9. PubMed ID: 12361551
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Frequency of HFE mutations among Turkish blood donors according to transferrin saturation: genotype screening for hereditary hemochromatosis among voluntary blood donors in Turkey.
    Simsek H; Sumer H; Yilmaz E; Balaban YH; Ozcebe O; Hascelik G; Buyukask Y; Tatar G
    J Clin Gastroenterol; 2004 Sep; 38(8):671-5. PubMed ID: 15319650
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.