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Items: 1 to 20 of 117

1.

Iron storage disease in Asia-Pacific populations: the importance of non-HFE mutations.

McDonald CJ, Wallace DF, Crawford DH, Subramaniam VN.

J Gastroenterol Hepatol. 2013 Jul;28(7):1087-94. doi: 10.1111/jgh.12222. Review.

PMID:
23577916
2.

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
3.

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.

5.

Analysis of HFE and non-HFE gene mutations in Brazilian patients with hemochromatosis.

Bittencourt PL, Marin ML, Couto CA, Cançado EL, Carrilho FJ, Goldberg AC.

Clinics (Sao Paulo). 2009;64(9):837-41. doi: 10.1590/S1807-59322009000900003.

6.

Hepatic iron metabolism gene expression profiles in HFE associated hereditary hemochromatosis.

Gleeson F, Ryan E, Barrett S, Russell J, Crowe J.

Blood Cells Mol Dis. 2007 Jan-Feb;38(1):37-44. Epub 2006 Nov 13.

PMID:
17098454
7.

Mutations of the HFE gene among Turkish hereditary hemochromatosis patients.

Simsek H, Balaban YH, Yilmaz E, Sumer H, Buyukasik Y, Cengiz C, Ozcebe O, Hascelik G, Tatar G.

Ann Hematol. 2005 Oct;84(10):646-9. Epub 2005 May 4.

PMID:
15871018
8.

Impact of HFE genetic testing on clinical presentation of hereditary hemochromatosis: new epidemiological data.

Scotet V, Le Gac G, Mérour MC, Mercier AY, Chanu B, Ka C, Mura C, Nousbaum JB, Férec C.

BMC Med Genet. 2005 Jun 1;6:24.

9.

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.

10.

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.

PMID:
11686223
11.

HFE and non-HFE hemochromatosis.

Anderson GJ, Powell LW.

Int J Hematol. 2002 Oct;76(3):203-7. Review.

PMID:
12416729
12.

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.

PMID:
12952143
13.

Hereditary hemochromatosis.

Fix OK, Kowdley KV.

Minerva Med. 2008 Dec;99(6):605-17. Review.

PMID:
19034258
14.

The haemochromatosis gene: a global perspective and implications for the Asia-Pacific region.

Mortimore M, Merryweather-Clarke AT, Robson KJ, Powell LW.

J Gastroenterol Hepatol. 1999 Sep;14(9):838-43. Review.

PMID:
10535463
15.

Analysis of haemochromatosis gene mutations in a population from the Mediterranean Basin.

Campo S, Restuccia T, Villari D, Raffa G, Cucinotta D, Squadrito G, Pollicino T, Raimondo G.

Liver. 2001 Aug;21(4):233-6.

PMID:
11454185
16.

HFE, hepcidin and ferroportin gene mutations are not present in Indian patients with primary haemochromatosis.

Shukla P, Julka S, Bhatia E, Shah S, Nagral A, Aggarwal R.

Natl Med J India. 2006 Jan-Feb;19(1):20-3.

PMID:
16570681
17.

HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing?

Santos PC, Pereira AC, Cançado RD, Schettert IT, Sobreira TJ, Oliveira PS, Hirata RD, Hirata MH, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM.

Blood Cells Mol Dis. 2010 Dec 15;45(4):302-7. doi: 10.1016/j.bcmd.2010.08.008. Epub 2010 Sep 16.

PMID:
20843714
18.

Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis.

Porto G, Alves H, Rodrigues P, Cabeda JM, Portal C, Ruivo A, Justiça B, Wolff R, De Sousa M.

Immunogenetics. 1998 Apr;47(5):404-10.

PMID:
9510559
19.

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.

20.

Screening for iron overload in the Turkish population.

Barut G, Balci H, Bozdayi M, Hatemi I, Ozcelik D, Senturk H.

Dig Dis. 2003;21(3):279-85.

PMID:
14571105
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