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Items: 1 to 20 of 168

1.

Hereditary hemochromatosis.

Crownover BK, Covey CJ.

Am Fam Physician. 2013 Feb 1;87(3):183-90. Review.

2.

[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
3.

Recent advances in hereditary hemochromatosis.

Franchini M, Veneri D.

Ann Hematol. 2005 Jun;84(6):347-52. Review.

PMID:
15747119
4.

Hemochromatosis and iron-overload screening in a racially diverse population.

Adams PC, Reboussin DM, Barton JC, McLaren CE, Eckfeldt JH, McLaren GD, Dawkins FW, Acton RT, Harris EL, Gordeuk VR, Leiendecker-Foster C, Speechley M, Snively BM, Holup JL, Thomson E, Sholinsky P; Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators..

N Engl J Med. 2005 Apr 28;352(17):1769-78.

5.

A population-based study of the clinical expression of the hemochromatosis gene.

Olynyk JK, Cullen DJ, Aquilia S, Rossi E, Summerville L, Powell LW.

N Engl J Med. 1999 Sep 2;341(10):718-24.

6.

[Hereditary hemochromatosis].

Niederau C.

Med Klin (Munich). 2009 Dec 15;104(12):931-46. doi: 10.1007/s00063-009-1192-6. Review. German.

PMID:
20039160
7.

HFE-associated hereditary hemochromatosis.

Alexander J, Kowdley KV.

Genet Med. 2009 May;11(5):307-13. doi: 10.1097/GIM.0b013e31819d30f2. Review.

PMID:
19444013
8.

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.

9.

Correlation between iron status and genetic hemochromatosis (codon C282Y) in a large German population.

Wrede CE, Hutzler S, Bollheimer LC, Buettner R, Hellerbrand C, Schöelmerich J, Palitzsch KD.

Isr Med Assoc J. 2004 Jan;6(1):30-3.

10.

[Hereditary hemochromatosis].

Dantas W.

Rev Gastroenterol Peru. 2001 Jan-Mar;21(1):42-55. Review. Portuguese.

PMID:
12170286
11.

Diagnosis and treatment of hereditary hemochromatosis: an update.

Kanwar P, Kowdley KV.

Expert Rev Gastroenterol Hepatol. 2013 Aug;7(6):517-30. doi: 10.1586/17474124.2013.816114. Review. Erratum in: Expert Rev Gastroenterol Hepatol. 2013 Nov;7(8):767.

PMID:
23985001
12.

When and how should we screen for hereditary hemochromatosis?

Chalès G, Guggenbuhl P.

Joint Bone Spine. 2003 Aug;70(4):263-70. Review.

PMID:
12951308
13.

Diagnosis and management of hereditary hemochromatosis.

Salgia RJ, Brown K.

Clin Liver Dis. 2015 Feb;19(1):187-98. doi: 10.1016/j.cld.2014.09.011. Review.

PMID:
25454304
14.

Hereditary hemochromatosis: missed diagnosis or misdiagnosis?

Cherfane CE, Hollenbeck RD, Go J, Brown KE.

Am J Med. 2013 Nov;126(11):1010-5. doi: 10.1016/j.amjmed.2013.07.013.

PMID:
24054178
15.

Examining the clinical use of hemochromatosis genetic testing.

Lanktree MB, Lanktree BB, Paré G, Waye JS, Sadikovic B, Crowther MA.

Can J Gastroenterol Hepatol. 2015 Jan-Feb;29(1):41-5.

16.

Hereditary hemochromatosis: insights from the Hemochromatosis and Iron Overload Screening (HEIRS) Study.

McLaren GD, Gordeuk VR.

Hematology Am Soc Hematol Educ Program. 2009:195-206. doi: 10.1182/asheducation-2009.1.195.

17.

HFE mutations in Caucasian participants of the Hemochromatosis and Iron Overload Screening study with serum ferritin level <1000 µg/L.

Adams PC, McLaren CE, Speechley M, McLaren GD, Barton JC, Eckfeldt JH.

Can J Gastroenterol. 2013 Jul;27(7):390-2.

18.

[Diagnosis of 5 patients with possible primary hemochromatosis].

Jacobs EM, de Vries RA, Elving LD, Stalenhoef AF, Swinkels DW.

Ned Tijdschr Geneeskd. 2003 Apr 5;147(14):666-70. Dutch.

PMID:
12712652
19.
20.

Increased risk of death from iron overload among 422 treated probands with HFE hemochromatosis and serum levels of ferritin greater than 1000 μg/L at diagnosis.

Barton JC, Barton JC, Acton RT, So J, Chan S, Adams PC.

Clin Gastroenterol Hepatol. 2012 Apr;10(4):412-6. doi: 10.1016/j.cgh.2011.11.032.

PMID:
22265917
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