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Similar articles for PubMed (Select 17474269)

1.

HFE mutation H63D predicts risk of iron over load in thalassemia intermedia irrespective of blood transfusions.

Sharma V, Panigrahi I, Dutta P, Tyagi S, Choudhry VP, Saxena R.

Indian J Pathol Microbiol. 2007 Jan;50(1):82-5.

PMID:
17474269
2.

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.

3.

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):651-5. Epub 2004 Nov 5.

PMID:
15538648
4.

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.

PMID:
11722599
5.

H63D mutation of the hemochromatosis gene and serum ferritin levels in Thai thalassemia carriers.

Yamsri S, Sanchaisuriya K, Fucharoen S, Fucharoen G, Jetsrisuparb A, Wiangnon S, Changtrakul Y, Sanchaisuriya P.

Acta Haematol. 2007;118(2):99-105. Epub 2007 Jul 18.

PMID:
17637512
6.

Hemochromatosis (HFE) gene mutations in Brazilian chronic hemodialysis patients.

Perícole FV, Alves MA, Saad ST, Costa FF.

Braz J Med Biol Res. 2005 Sep;38(9):1321-4. Epub 2005 Aug 26.

7.

Analysis of HFE gene mutations and HLA-A alleles in Brazilian patients with iron overload.

Cançado RD, Guglielmi AC, Vergueiro CS, Rolim EG, Figueiredo MS, Chiattone CS.

Sao Paulo Med J. 2006 Mar 2;124(2):55-60.

8.

[HFE gene mutations in Tunisian major beta-Thalassemia and iron overload].

Mellouli F, El Borgi W, Kaabi H, Ben Hassen E, Sassi R, Hmida H, Cherif G, Maamar M, Zouari B, Boukef K, Bejaoui M, Hmida S.

Transfus Clin Biol. 2006 Dec;13(6):353-7. Epub 2007 Feb 15. French.

PMID:
17303462
9.

The impact of the mutations of the HFE gene and of the SLC11A3 gene on iron overload in Greek thalassemia intermedia and beta(s)/beta(thal) anemia patients.

Politou M, Kalotychou V, Pissia M, Rombos Y, Sakellaropoulos N, Papanikolaou G.

Haematologica. 2004 Apr;89(4):490-2.

10.

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 Mar-Apr;53(2):117-20.

PMID:
11421105
11.

[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. Slovak.

PMID:
16871764
12.

Individuals homozygous for the H63D mutation have significantly elevated iron indexes.

Samarasena J, Winsor W, Lush R, Duggan P, Xie Y, Borgaonkar M.

Dig Dis Sci. 2006 Apr;51(4):803-7.

PMID:
16615007
13.

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.

PMID:
10870847
14.

Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000).

Martinelli AL, Filho R, Cruz S, Franco R, Tavella M, Secaf M, Ramalho L, Zucoloto S, Rodrigues S, Zago M.

Genet Mol Res. 2005 Mar 31;4(1):31-8.

15.

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.

16.

Iron status and HFE genotype in erythrocyte pyruvate kinase deficiency: study of Italian cases.

Zanella A, Bianchi P, Iurlo A, Boschetti C, Taioli E, Vercellati C, Zappa M, Fermo E, Tavazzi D, Sampietro M.

Blood Cells Mol Dis. 2001 May-Jun;27(3):653-61.

PMID:
11482880
17.

Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorder.

Viprakasit V, Vathesathokit P, Chinchang W, Tachavanich K, Pung-Amritt P, Wimhurst VL, Yenchitsomanus PT, Merryweather-Clarke AT, Tanphaichitr VS.

Eur J Haematol. 2004 Jul;73(1):43-9.

PMID:
15182337
18.

Hereditary hemochromatosis: the clinical significance of the S65C mutation.

Asberg A, Thorstensen K, Hveem K, Bjerve KS.

Genet Test. 2002 Spring;6(1):59-62.

PMID:
12180078
19.

HFE mutations do not account for transfusional iron overload in patients with acute myeloid leukemia.

Parkkila S, Niemelä O, Savolainen ER, Koistinen P.

Transfusion. 2001 Jun;41(6):828-31.

PMID:
11399828
20.

Mutations of the hemochromatosis gene in Italian candidate blood donors with increased transferrin saturation.

Velati C, Marlianici E, Rigamonti D, Barillari G, Chiavilli F, Fugiani P, Garozzo G, Lancieri M, Rinaldi S, Testa D, Sampietro M, Tavazzi D, Delbini P, Fargion S, Fiorelli G.

Hematol J. 2003;4(6):436-40.

PMID:
14671617
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