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Items: 1 to 20 of 162

1.

New insights into iron homeostasis through the study of non-HFE hereditary haemochromatosis.

Roetto A, Camaschella C.

Best Pract Res Clin Haematol. 2005 Jun;18(2):235-50. Review.

PMID:
15737887
2.

Non-HFE haemochromatosis.

Wallace DF, Subramaniam VN.

World J Gastroenterol. 2007 Sep 21;13(35):4690-8. Review.

3.

Non-HFE hemochromatosis.

Pietrangelo A.

Semin Liver Dis. 2005 Nov;25(4):450-60. Review.

PMID:
16315138
4.

Disrupted hepcidin regulation in HFE-associated haemochromatosis and the liver as a regulator of body iron homoeostasis.

Bridle KR, Frazer DM, Wilkins SJ, Dixon JL, Purdie DM, Crawford DH, Subramaniam VN, Powell LW, Anderson GJ, Ramm GA.

Lancet. 2003 Feb 22;361(9358):669-73.

PMID:
12606179
5.

[Non-HFE-related hereditary iron overload].

Aguilar-Martinez P.

Presse Med. 2007 Sep;36(9 Pt 2):1279-91. Epub 2007 May 30. Review. French.

PMID:
17540536
6.

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
7.

The molecular pathogenesis of hereditary hemochromatosis.

Babitt JL, Lin HY.

Semin Liver Dis. 2011 Aug;31(3):280-92. doi: 10.1055/s-0031-1286059. Epub 2011 Sep 7. Review.

PMID:
21901658
8.

Function of the hemochromatosis protein HFE: Lessons from animal models.

Pantopoulos K.

World J Gastroenterol. 2008 Dec 7;14(45):6893-901.

9.

Genetic haemochromatosis: genes and mutations associated with iron loading.

Camaschella C, Roetto A, De Gobbi M.

Best Pract Res Clin Haematol. 2002 Jun;15(2):261-76. Review.

PMID:
12401307
10.

Review article: the genetic basis of haemochromatosis.

Griffiths WJ.

Aliment Pharmacol Ther. 2007 Aug 1;26(3):331-42. Review.

11.

Hemochromatosis: genetics and pathophysiology.

Beutler E.

Annu Rev Med. 2006;57:331-47. Review.

PMID:
16409153
12.

Defective release of Hepcidin not defective synthesis is the primary pathogenic mechanism in HFE-Haemochromatosis.

Arnold J, Sangwaiya A, Bhatkal B, Arnold A.

Med Hypotheses. 2008;70(6):1197-200. Epub 2007 Dec 3.

PMID:
18054440
13.

Hereditary iron overload: update on pathophysiology, diagnosis, and treatment.

Franchini M.

Am J Hematol. 2006 Mar;81(3):202-9. Review.

14.

[Pathophysiology and genetics of classic HFE (type 1) hemochromatosis].

Loréal O, Ropert M, Mosser A, Déhais V, Deugnier Y, David V, Brissot P, Jouanolle AM.

Presse Med. 2007 Sep;36(9 Pt 2):1271-7. Epub 2007 May 22. Review. French.

PMID:
17521857
15.

Regulatory networks for the control of body iron homeostasis and their dysregulation in HFE mediated hemochromatosis.

Ludwiczek S, Theurl I, Bahram S, Schümann K, Weiss G.

J Cell Physiol. 2005 Aug;204(2):489-99.

PMID:
15744772
16.

Molecular insights into the pathogenesis of hereditary haemochromatosis.

Pietrangelo A.

Gut. 2006 Apr;55(4):564-8. Review. No abstract available.

17.

Genetics, Genetic Testing, and Management of Hemochromatosis: 15 Years Since Hepcidin.

Pietrangelo A.

Gastroenterology. 2015 Oct;149(5):1240-1251.e4. doi: 10.1053/j.gastro.2015.06.045. Epub 2015 Jul 9. Review.

PMID:
26164493
18.

[Hereditary haemochromatosis: novel genes, novel diseases and hepcidin].

Bergmans JP, Kemna EH, Janssen MC, Jacobs EM, Stalenhoef AF, Marx JJ, Swinkels DW.

Ned Tijdschr Geneeskd. 2007 May 19;151(20):1121-7. Review. Dutch.

PMID:
17557668
19.

Interaction of the hereditary hemochromatosis protein HFE with transferrin receptor 2 is required for transferrin-induced hepcidin expression.

Gao J, Chen J, Kramer M, Tsukamoto H, Zhang AS, Enns CA.

Cell Metab. 2009 Mar;9(3):217-27. doi: 10.1016/j.cmet.2009.01.010.

20.

Iron disorders of genetic origin: a changing world.

Brissot P, Bardou-Jacquet E, Jouanolle AM, Loréal O.

Trends Mol Med. 2011 Dec;17(12):707-13. doi: 10.1016/j.molmed.2011.07.004. Epub 2011 Aug 20. Review.

PMID:
21862411

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