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 *

298 related articles for article (PubMed ID: 11122155)

  • 1. Haemochromatosis in patients with beta-thalassaemia trait.
    Piperno A; Mariani R; Arosio C; Vergani A; Bosio S; Fargion S; Sampietro M; Girelli D; Fraquelli M; Conte D; Fiorelli G; Camaschella C
    Br J Haematol; 2000 Dec; 111(3):908-14. PubMed ID: 11122155
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Heterozygosity for the H63D mutation in the hereditary hemochromatosis (HFE) gene may lead into severe iron overload in beta-thalassemia minor: observations in a thalassemic kindred.
    Ruiz-Argüelles GJ; Garcés-Eisele J; Reyes-Núñez V; Sánchez-Anzaldo J; Ruiz-Delgado GJ; Jiménez-González C; Carrera B
    Rev Invest Clin; 2001; 53(2):117-20. PubMed ID: 11421105
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The influence of hemochromatosis mutations on iron overload of thalassemia major.
    Longo F; Zecchina G; Sbaiz L; Fischer R; Piga A; Camaschella C
    Haematologica; 1999 Sep; 84(9):799-803. PubMed ID: 10477452
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Distribution of C282Y and H63D mutations in the HFE gene in healthy Asian Indians and patients with thalassaemia major.
    Kaur G; Rapthap CC; Xavier M; Saxena R; Choudhary VP; Reuben SK; Mehra NK
    Natl Med J India; 2003; 16(6):309-10. PubMed ID: 14765621
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Noniatrogenic haemochromatosis in congenital dyserythropoietic anaemia type II is not related to C282Y and H63D mutations in the HFE gene: report on two brothers.
    Van Steenbergen W; Matthijs G; Roskams T; Fevery J
    Acta Clin Belg; 2002; 57(2):79-84. PubMed ID: 12152243
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. HFE haemochromatosis gene mutations in liver transplant patients.
    Halme L; Heliö T; Mäkinen J; Höckerstedt K; Färkkilä M; Piippo K; Krusius T; Kontula K
    Scand J Gastroenterol; 2001 Aug; 36(8):881-5. PubMed ID: 11495086
    [TBL] [Abstract][Full Text] [Related]  

  • 8. DNA testing for haemochromatosis: diagnostic, predictive and screening implications.
    Trent RJ; Le H; Yu B; Young G; Bowden DK
    Pathology; 2000 Nov; 32(4):274-9. PubMed ID: 11186424
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The C282Y mutation of the HFE gene is not found in Chinese haemochromatotic patients: multicentre retrospective study.
    Tsui WM; Lam PW; Lee KC; Ma KF; Chan YK; Wong MW; Yip SP; Wong CS; Chow AS; Lo ST
    Hong Kong Med J; 2000 Jun; 6(2):153-8. PubMed ID: 10895137
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Frequency of HFE gene mutations in Iranian beta-thalassaemia minor patients.
    Jazayeri M; Bakayev V; Adibi P; Haghighi Rad F; Zakeri H; Kalantar E; Zali MR
    Eur J Haematol; 2003 Dec; 71(6):408-11. PubMed ID: 14703689
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hereditary haemochromatosis: diagnosis and management in the gene era.
    Olynyk JK
    Liver; 1999 Apr; 19(2):73-80. PubMed ID: 10220735
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Haemochromatosis and HFE gene.
    Moirand R; Deugnier Y; Brissot P
    Acta Gastroenterol Belg; 1999; 62(4):403-9. PubMed ID: 10692770
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Iron in the era of molecular biology].
    Deugnier Y; Moirand R; Brissot P; David V
    Pathol Biol (Paris); 1999 Nov; 47(9):938-44. PubMed ID: 10609274
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Effect of co-inheritance of β-thalassemia and hemochromatosis mutations on iron overload.
    López-Escribano H; Ferragut JF; Parera MM; Guix P; Castro JA; Ramon MM; Picornell A
    Hemoglobin; 2012; 36(1):85-92. PubMed ID: 22122796
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Inherited HFE-unrelated hemochromatosis in Italian families.
    Camaschella C; Fargion S; Sampietro M; Roetto A; Bosio S; Garozzo G; Arosio C; Piperno A
    Hepatology; 1999 May; 29(5):1563-4. PubMed ID: 10216143
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Relation between HFE mutations and mild iron-overload expression.
    Mura C; Le Gac G; Raguénes O; Mercier AY; Le Guen A; Férec C
    Mol Genet Metab; 2000 Apr; 69(4):295-301. PubMed ID: 10870847
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Role of HFE gene mutations on developing iron overload in beta-thalassaemia carriers in Egypt.
    Madani HA; Afify RA; Abd El-Aal AA; Salama N; Ramy N
    East Mediterr Health J; 2011 Jun; 17(6):546-51. PubMed ID: 21796974
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Haemochromatosis gene mutations and risk of coronary artery disease.
    Battiloro E; Ombres D; Pascale E; D'Ambrosio E; Verna R; Arca M
    Eur J Hum Genet; 2000 May; 8(5):389-92. PubMed ID: 10854101
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prevalence and clinical significance of HFE gene mutations in patients with iron overload.
    Brandhagen DJ; Fairbanks VF; Baldus WP; Smith CI; Kruckeberg KE; Schaid DJ; Thibodeau SN
    Am J Gastroenterol; 2000 Oct; 95(10):2910-4. PubMed ID: 11051367
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.