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 *

149 related articles for article (PubMed ID: 10627947)

  • 1. Evidence from a Ghanaian population of known African descent to support the proposition that hemochromatosis is a Caucasian disorder.
    Jeffery S; Crosby A; Plange-Rhule J; Amoah-Danquah J; Acheampong JW; Eastwood JB; Malik AK
    Genet Test; 1999; 3(4):375-7. PubMed ID: 10627947
    [TBL] [Abstract][Full Text] [Related]  

  • 2. HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology.
    Hanson EH; Imperatore G; Burke W
    Am J Epidemiol; 2001 Aug; 154(3):193-206. PubMed ID: 11479183
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis.
    Bittencourt PL; Palácios SA; Couto CA; Cançado EL; Carrilho FJ; Laudanna AA; Kalil J; Gayotto LC; Goldberg AC
    Braz J Med Biol Res; 2002 Mar; 35(3):329-35. PubMed ID: 11887210
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Transferrin receptor-2 (TFR2) mutation Y250X in Alabama Caucasian and African American subjects with and without primary iron overload.
    Barton EH; West PA; Rivers CA; Barton JC; Acton RT
    Blood Cells Mol Dis; 2001; 27(1):279-84. PubMed ID: 11358388
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inheritance of two HFE mutations in African Americans: cases with hemochromatosis phenotypes and estimates of hemochromatosis phenotype frequency.
    Barton JC; Acton RT
    Genet Med; 2001; 3(4):294-300. PubMed ID: 11478530
    [TBL] [Abstract][Full Text] [Related]  

  • 7. HFE gene mutations an Apulian population: allele frequencies.
    Pietrapertosa A; Vitucci A; Campanale D; Palma A; Renni R; Delios G; Tannoia N
    Eur J Epidemiol; 2003; 18(7):685-9. PubMed ID: 12952143
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay.
    Cukjati M; Vaupotic T; Rupreht R; Curin-Serbec V
    BMC Med Genet; 2007 Nov; 8():69. PubMed ID: 18036208
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Prevalence of hemochromatosis-associated mutations in the hemochromatosis gene in the Danish population].
    Larsen LE; Ellervik C; Appleyard M; Nordestgaard BG; Birgens H; Tybjaerg-Hansen A
    Ugeskr Laeger; 2002 Sep; 164(39):4545-7. PubMed ID: 12380399
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prevalence and penetrance of HFE mutations in 4865 unselected primary care patients.
    Phatak PD; Ryan DH; Cappuccio J; Oakes D; Braggins C; Provenzano K; Eberly S; Sham RL
    Blood Cells Mol Dis; 2002; 29(1):41-7. PubMed ID: 12482402
    [TBL] [Abstract][Full Text] [Related]  

  • 11. HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania.
    Trifa AP; Popp RA; Militaru MS; Farcaş MF; Crişan TO; Gana I; Cucuianu A; Pop IV
    J Gastrointestin Liver Dis; 2012 Jun; 21(2):177-80. PubMed ID: 22720307
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.
    Aguilar-Martinez P; Esculié-Coste C; Bismuth M; Giansily-Blaizot M; Larrey D; Schved JF
    Blood Cells Mol Dis; 2001; 27(1):290-3. PubMed ID: 11358390
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prevalence of HFE gene C282Y and H63D mutations in a French-Canadian population of neonates and in referred patients.
    Girouard J; Giguère Y; Delage R; Rousseau F
    Hum Mol Genet; 2002 Jan; 11(2):185-9. PubMed ID: 11809727
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Geography of HFE C282Y and H63D mutations.
    Merryweather-Clarke AT; Pointon JJ; Jouanolle AM; Rochette J; Robson KJ
    Genet Test; 2000; 4(2):183-98. PubMed ID: 10953959
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation.
    Gochee PA; Powell LW; Cullen DJ; Du Sart D; Rossi E; Olynyk JK
    Gastroenterology; 2002 Mar; 122(3):646-51. PubMed ID: 11874997
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
    Sham RL; Ou CY; Cappuccio J; Braggins C; Dunnigan K; Phatak PD
    Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutation analysis of the HFE gene in Brazilian populations.
    Agostinho MF; Arruda VR; Basseres DS; Bordin S; Soares MC; Menezes RC; Costa FF; Saad ST
    Blood Cells Mol Dis; 1999; 25(5-6):324-7. PubMed ID: 10660479
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Geographic and racial/ethnic differences in HFE mutation frequencies in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.
    Acton RT; Barton JC; Snively BM; McLaren CE; Adams PC; Harris EL; Speechley MR; McLaren GD; Dawkins FW; Leiendecker-Foster C; Holup JL; Balasubramanyam A;
    Ethn Dis; 2006; 16(4):815-21. PubMed ID: 17061732
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote.
    Wallace DF; Dooley JS; Walker AP
    Gastroenterology; 1999 Jun; 116(6):1409-12. PubMed ID: 10348824
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.