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Items: 1 to 20 of 95

1.

High prevalence of fibromyalgia in patients with HFE-related hereditary hemochromatosis.

Mohammad A, Carey JJ, Storan E, Scarry M, Coughlan RJ, Lee JM.

J Clin Gastroenterol. 2013 Jul;47(6):559-64. doi: 10.1097/MCG.0b013e31826f7ad7.

PMID:
23188073
2.

Prevalence of fibromyalgia among patients with chronic hepatitis C infection: relationship to viral characteristics and quality of life.

Mohammad A, Carey JJ, Storan E, Scarry M, Coughlan RJ, Lee JM.

J Clin Gastroenterol. 2012 May-Jun;46(5):407-12. doi: 10.1097/MCG.0b013e3182485528.

PMID:
22499073
4.

Mutations in HFE causing hemochromatosis are associated with primary hypertriglyceridemia.

Solanas-Barca M, Mateo-Gallego R, Calmarza P, Jarauta E, Bea AM, Cenarro A, Civeira F.

J Clin Endocrinol Metab. 2009 Nov;94(11):4391-7. doi: 10.1210/jc.2009-0814. Epub 2009 Oct 9.

PMID:
19820015
5.

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.

6.

Patatin-like phospholipase domain containing-3 gene I148M polymorphism, steatosis, and liver damage in hereditary hemochromatosis.

Valenti L, Maggioni P, Piperno A, Rametta R, Pelucchi S, Mariani R, Dongiovanni P, Fracanzani AL, Fargion S.

World J Gastroenterol. 2012 Jun 14;18(22):2813-20. doi: 10.3748/wjg.v18.i22.2813.

8.

HFE C282Y/H63D compound heterozygotes are at low risk of hemochromatosis-related morbidity.

Gurrin LC, Bertalli NA, Dalton GW, Osborne NJ, Constantine CC, McLaren CE, English DR, Gertig DM, Delatycki MB, Nicoll AJ, Southey MC, Hopper JL, Giles GG, Anderson GJ, Olynyk JK, Powell LW, Allen KJ; HealthIron Study Investigators.

Hepatology. 2009 Jul;50(1):94-101. doi: 10.1002/hep.22972.

9.

HFE Cys282Tyr homozygotes with serum ferritin concentrations below 1000 microg/L are at low risk of hemochromatosis.

Allen KJ, Bertalli NA, Osborne NJ, Constantine CC, Delatycki MB, Nisselle AE, Nicoll AJ, Gertig DM, McLaren CE, Giles GG, Hopper JL, Anderson GJ, Olynyk JK, Powell LW, Gurrin LC; HealthIron Study Investigators.

Hepatology. 2010 Sep;52(3):925-33. doi: 10.1002/hep.23786.

10.

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
11.

Association of porphyria cutanea tarda with hereditary hemochromatosis.

Mehrany K, Drage LA, Brandhagen DJ, Pittelkow MR.

J Am Acad Dermatol. 2004 Aug;51(2):205-11.

PMID:
15280838
12.

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.

13.

Non-alcoholic steatohepatitis and iron: increased prevalence of mutations of the HFE gene in non-alcoholic steatohepatitis.

Bonkovsky HL, Jawaid Q, Tortorelli K, LeClair P, Cobb J, Lambrecht RW, Banner BF.

J Hepatol. 1999 Sep;31(3):421-9.

PMID:
10488699
14.

Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis.

Lawless MW, White M, Mankan AK, O'Dwyer MJ, Norris S.

Tissue Antigens. 2007 Oct;70(4):294-300.

PMID:
17767550
15.

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
16.

Hereditary hemochromatosis: awareness and genetic testing acceptability in Western Romania.

Neghina AM, Anghel A.

Genet Test Mol Biomarkers. 2010 Dec;14(6):847-50. doi: 10.1089/gtmb.2010.0109. Epub 2010 Oct 28.

PMID:
20979574
17.

Iron-overload-related disease in HFE hereditary hemochromatosis.

Allen KJ, Gurrin LC, Constantine CC, Osborne NJ, Delatycki MB, Nicoll AJ, McLaren CE, Bahlo M, Nisselle AE, Vulpe CD, Anderson GJ, Southey MC, Giles GG, English DR, Hopper JL, Olynyk JK, Powell LW, Gertig DM.

N Engl J Med. 2008 Jan 17;358(3):221-30. doi: 10.1056/NEJMoa073286.

18.

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.

19.

Prevalence of coronary heart disease associated with HFE mutations in adults attending a health appraisal center.

Waalen J, Felitti V, Gelbart T, Ho NJ, Beutler E.

Am J Med. 2002 Oct 15;113(6):472-9.

PMID:
12427496

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