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Items: 1 to 20 of 110

1.

Molecular epidemiology of HFE gene polymorphic variants (C282Y, H63D and S65C) in the population of Espírito Santo, Brazil.

Alves LN, Santos EV, Stur E, Silva Conforti AM, Louro ID.

Genet Mol Res. 2016 Apr 27;15(2). doi: 10.4238/gmr.15028189.

3.

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.

4.

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.

5.

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. Epub 2004 Oct 29.

PMID:
15517265
6.

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. doi: 10.1007/s00277-011-1338-5. Epub 2011 Sep 27.

PMID:
21947086
7.

Analysis of the HFE gene (C282Y, H63D and S65C) mutations in a general Chinese Han population.

Lin A, Yan WH, Xu HH, Zhu M, Zhou MY.

Tissue Antigens. 2007 Sep;70(3):252-5.

PMID:
17661915
8.

Frequency of HFE H63D, S65C, and C282Y mutations in patients with iron overload and controls from Toledo, Spain.

de Diego C, Murga MJ, Martínez-Castro P.

Genet Test. 2004 Fall;8(3):263-7.

PMID:
15727249
9.

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. doi: 10.3233/DMA-2009-0642.

10.

Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients.

Santos PC, Cançado RD, Pereira AC, Schettert IT, Soares RA, Pagliusi RA, Hirata RD, Hirata MH, Teixeira AC, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM.

Blood Cells Mol Dis. 2011 Apr 15;46(4):302-7. doi: 10.1016/j.bcmd.2011.02.008.

PMID:
21411349
11.

Prevalence of H63D, S65C, and C282Y hereditary hemochromatosis gene variants in Madeira Island (Portugal).

Spínola C, Brehm A, Spínola H.

Ann Hematol. 2011 Jan;90(1):29-32. doi: 10.1007/s00277-010-1034-x. Epub 2010 Aug 17.

PMID:
20714725
12.

Frequency of the hemochromatosis HFE mutations C282Y, H63D, and S65C in blood donors in the Faroe Islands.

Milman N, á Steig T, Koefoed P, Pedersen P, Fenger K, Nielsen FC.

Ann Hematol. 2005 Mar;84(3):146-9. Epub 2004 Mar 23.

PMID:
15042317
13.

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 Jr, Maciel JF, de Freitas RV, de Souza Paiva A, Cavalcanti GB Jr.

J Clin Lab Anal. 2014 May;28(3):178-85. doi: 10.1002/jcla.21663. Epub 2014 Jan 6.

14.

[The importance of DNA analysis of C282Y, H63D and S65C mutations in the HFE gene].

Drastíková M, Beránek M, Hegerová J, Putzová D.

Cas Lek Cesk. 2012;151(9):428-31. Czech.

PMID:
23102134
15.

Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants.

Pedersen P, Milman N.

Ann Hematol. 2009 Aug;88(8):775-84. doi: 10.1007/s00277-008-0679-1. Epub 2009 Jan 22.

PMID:
19159930
16.

S65C and other mutations in the haemochromatosis gene in the Czech population.

Cimburová M, Půtová I, Provazníková H, Pintérová D, Horák J.

Folia Biol (Praha). 2005;51(6):172-6.

17.
18.

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.

19.

Simultaneous detection of HFE C282Y, H63D and S65C mutations associated with type 1 haemochromatosis using a multiplex luminex bead assay.

Cardoso SP, Patel R, Brown C, Navarrete C.

Tissue Antigens. 2011 Sep;78(3):171-7. doi: 10.1111/j.1399-0039.2011.01736.x. Epub 2011 Jul 8.

PMID:
21736562
20.

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. Epub 2005 Nov 12.

PMID:
15995871

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