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Items: 1 to 20 of 40

1.

Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.

Benyamin B, McRae AF, Zhu G, Gordon S, Henders AK, Palotie A, Peltonen L, Martin NG, Montgomery GW, Whitfield JB, Visscher PM.

Am J Hum Genet. 2009 Jan;84(1):60-5. doi: 10.1016/j.ajhg.2008.11.011. Epub 2008 Dec 11.

2.

[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
3.

[Management of hemochromatosis linked to HFE gene].

Brissot P, De Bels F.

Presse Med. 2007 Sep;36(9 Pt 2):1295-300. Epub 2007 Jun 5. Review. French.

PMID:
17553656
4.

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
5.

The enigmatic role of the hemochromatosis protein (HFE) in iron absorption.

Chorney MJ, Yoshida Y, Meyer PN, Yoshida M, Gerhard GS.

Trends Mol Med. 2003 Mar;9(3):118-25. Review.

PMID:
12657433
6.

Genetic background of primary iron overload syndromes in Japan.

Hayashi H, Wakusawa S, Motonishi S, Miyamoto K, Okada H, Inagaki Y, Ikeda T.

Intern Med. 2006;45(20):1107-11. Epub 2006 Nov 15. Review.

7.

Changing aspects of HFE-related hereditary haemochromatosis and endeavours to early diagnosis.

Jacobs EM, Verbeek AL, Kreeftenberg HG, van Deursen CT, Marx JJ, Stalenhoef AF, Swinkels DW, de Vries RA.

Neth J Med. 2007 Dec;65(11):419-24. Review.

8.

Iron overload syndromes and the liver.

Batts KP.

Mod Pathol. 2007 Feb;20 Suppl 1:S31-9. Review.

9.

Hereditary haemochromatosis.

Janssen MC, Swinkels DW.

Best Pract Res Clin Gastroenterol. 2009;23(2):171-83. doi: 10.1016/j.bpg.2009.02.004. Review.

PMID:
19414144
10.

The regulation of cellular iron metabolism.

Chua AC, Graham RM, Trinder D, Olynyk JK.

Crit Rev Clin Lab Sci. 2007;44(5-6):413-59. Review.

PMID:
17943492
11.

Hereditary hemochromatosis.

Fix OK, Kowdley KV.

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

PMID:
19034258
12.

Hereditary hemochromatosis: pathophysiology, diagnosis, and management.

Fowler C.

Crit Care Nurs Clin North Am. 2008 Jun;20(2):191-201, vi. doi: 10.1016/j.ccell.2008.01.003. Review.

PMID:
18424348
13.

[Novel aspects of pathogenesis of hereditary hemochromatosis].

Raszeja-Wyszomirska J, Ławniczak M, Milkiewicz P.

Pol Merkur Lekarski. 2008 Jan;24(139):54-8. Review. Polish.

PMID:
18634255
14.

Hereditary hemochromatosis.

Franchini M, Veneri D.

Hematology. 2005 Apr;10(2):145-9. Review.

PMID:
16019461
15.

Transferrin receptor 1.

Aisen P.

Int J Biochem Cell Biol. 2004 Nov;36(11):2137-43. Review.

PMID:
15313461
16.

Liver and iron metabolism--a comprehensive hypothesis for the pathogenesis of genetic hemochromatosis.

Stremmel W, Karner M, Manzhalii E, Gilles W, Herrmann T, Merle U.

Z Gastroenterol. 2007 Jan;45(1):71-5. Review.

PMID:
17236123
17.

[Iron metabolism and its exploration in clinical biology].

Brissot P, Pigeon C, Moirand R, Guyader D, Mendler MH, Sapey T, Deugnier Y, Lescoat G, Loréal O.

Ann Biol Clin (Paris). 1998 Jul;56 Spec No:5-10. Review. French. No abstract available.

PMID:
9827209
18.

The molecular regulation of iron metabolism.

Donovan A, Andrews NC.

Hematol J. 2004;5(5):373-80. Review.

PMID:
15448662
19.

[Hemochromatosis--from an underdiagnosed curiosity to a common disease].

Hagve TA, Asberg A, Ulvik R, Borch-Iohnsen B, Thorstensen K.

Tidsskr Nor Laegeforen. 2009 Apr 30;129(9):863-6. doi: 10.4045/tidsskr.08.0084. Review. Norwegian.

20.

Diagnostic value of transferrin.

Szőke D, Panteghini M.

Clin Chim Acta. 2012 Aug 16;413(15-16):1184-9. doi: 10.1016/j.cca.2012.04.021. Epub 2012 Apr 23. Review.

PMID:
22546612
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