768 related articles for article (PubMed ID: 10942923)
1. Abnormal regulation of HFE mRNA expression does not contribute to primary iron overload.
Vercesi E; Cerani P; Rolandi V; Rovati A; Bergamaschi G
Haematologica; 2000 Aug; 85(8):787-91. PubMed ID: 10942923
[TBL] [Abstract][Full Text] [Related]
2. Differential HFE allele expression in hemochromatosis heterozygotes.
Rosmorduc O; Poupon R; Nion I; Wendum D; Feder J; Béréziat G; Hermelin B
Gastroenterology; 2000 Oct; 119(4):1075-86. PubMed ID: 11040194
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Clinical and genetic heterogeneity in hereditary haemochromatosis: association between lymphocyte counts and expression of iron overload.
Porto G; Cardoso CS; Gordeuk V; Cruz E; Fraga J; Areias J; Oliveira JC; Bravo F; Gangaidzo IT; MacPhail AP; Gomo ZA; Moyo VM; Melo G; Silva C; Justiça B; de Sousa M
Eur J Haematol; 2001 Aug; 67(2):110-8. PubMed ID: 11722599
[TBL] [Abstract][Full Text] [Related]
6. Mutation analysis of the HFE gene associated with hereditary hemochromatosis in a Venezuelan sample.
Vizzi E; Loureiro CL; Gerder M; de las Nieves Garcia-Casal M; Rodríguez-Larralde A; Gerace L; Ludert JE; Liprandi F; Pujol FH
Ann Hematol; 2005 Nov; 84(12):802-6. PubMed ID: 15995871
[TBL] [Abstract][Full Text] [Related]
7. [Molecular genetic diagnostics and screening of hereditary hemochromatosis].
Zlocha J; Kovács L; Pozgayová S; Kupcová V; Durínová S
Vnitr Lek; 2006 Jun; 52(6):602-8. PubMed ID: 16871764
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
12. A primer for predicting risk of disease in HFE-linked hemochromatosis.
Adams PC; Walker AP; Acton RT
Genet Test; 2001; 5(4):311-6. PubMed ID: 11960576
[TBL] [Abstract][Full Text] [Related]
13. Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population.
Kucinskas L; Juzenas S; Sventoraityte J; Cedaviciute R; Vitkauskiene A; Kalibatas V; Kondrackiene J; Kupcinskas L
Ann Hematol; 2012 Apr; 91(4):491-5. PubMed ID: 21947086
[TBL] [Abstract][Full Text] [Related]
14. Mutation analysis of the HFE gene in German hemochromatosis patients and controls using automated SSCP-based capillary electrophoresis and a new PCR-ELISA technique.
Hellerbrand C; Bosserhoff AK; Seegers S; Lingner G; Wrede C; Lock G; Schölmerich J; Büttner R
Scand J Gastroenterol; 2001 Nov; 36(11):1211-6. PubMed ID: 11686223
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. HFE based re-evaluation of heterozygous hemochromatosis.
Moirand R; Guyader D; Mendler MH; Jouanolle AM; Le Gall JY; David V; Brissot P; Deugnier Y
Am J Med Genet; 2002 Sep; 111(4):356-61. PubMed ID: 12210292
[TBL] [Abstract][Full Text] [Related]
17. A genotypic study of 217 unrelated probands diagnosed as "genetic hemochromatosis" on "classical" phenotypic criteria.
Brissot P; Moirand R; Jouanolle AM; Guyader D; Le Gall JY; Deugnier Y; David V
J Hepatol; 1999 Apr; 30(4):588-93. PubMed ID: 10207799
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. Update on hereditary hemochromatosis and the HFE gene.
Brandhagen DJ; Fairbanks VF; Batts KP; Thibodeau SN
Mayo Clin Proc; 1999 Sep; 74(9):917-21. PubMed ID: 10488796
[TBL] [Abstract][Full Text] [Related]
20. Compound heterozygotes for hemochromatosis gene mutations: may they help to understand the pathophysiology of the disease?
Aguilar Martinez P; Biron C; Blanc F; Masmejean C; Jeanjean P; Michel H; Schved JF
Blood Cells Mol Dis; 1997 Aug; 23(2):269-76. PubMed ID: 9410470
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]