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Page 1
Current approach to hemochromatosis.
Brissot P, Troadec MB, Bardou-Jacquet E, Le Lan C, Jouanolle AM, Deugnier Y, Loréal O. Brissot P, et al. Among authors: jouanolle am. Blood Rev. 2008 Jul;22(4):195-210. doi: 10.1016/j.blre.2008.03.001. Epub 2008 Apr 21. Blood Rev. 2008. PMID: 18430498 Review.
HFE based re-evaluation of heterozygous hemochromatosis.
Moirand R, Guyader D, Mendler MH, Jouanolle AM, Le Gall JY, David V, Brissot P, Deugnier Y. Moirand R, et al. Among authors: jouanolle am. Am J Med Genet. 2002 Sep 1;111(4):356-61. doi: 10.1002/ajmg.10547. Am J Med Genet. 2002. PMID: 12210292
[Genetic iron overload diseases: a deeply changing world].
Brissot P, Troadec MB, Le Lan C, Lorho R, Gaboriau F, Lescoat G, Jouanolle AM, Loréal O. Brissot P, et al. Among authors: jouanolle am. Nephrol Ther. 2006 Nov;2 Suppl 5:S298-303. Nephrol Ther. 2006. PMID: 17373274 Review. French.
[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. Loréal O, et al. Among authors: jouanolle am. Presse Med. 2007 Sep;36(9 Pt 2):1271-7. doi: 10.1016/j.lpm.2007.03.038. Epub 2007 May 22. Presse Med. 2007. PMID: 17521857 Review. French.
[Screening for hereditary HFE hemochromatosis].
Deugnier Y, Jouanolle AM. Deugnier Y, et al. Among authors: jouanolle am. Presse Med. 2007 Sep;36(9 Pt 2):1292-4. doi: 10.1016/j.lpm.2006.12.037. Epub 2007 Jun 4. Presse Med. 2007. PMID: 17544612 French.
Iron disorders of genetic origin: a changing world.
Brissot P, Bardou-Jacquet E, Jouanolle AM, Loréal O. Brissot P, et al. Among authors: jouanolle am. Trends Mol Med. 2011 Dec;17(12):707-13. doi: 10.1016/j.molmed.2011.07.004. Epub 2011 Aug 20. Trends Mol Med. 2011. PMID: 21862411 Review.
A novel N491S mutation in the human SLC11A2 gene impairs protein trafficking and in association with the G212V mutation leads to microcytic anemia and liver iron overload.
Bardou-Jacquet E, Island ML, Jouanolle AM, Détivaud L, Fatih N, Ropert M, Brissot E, Mosser A, Maisonneuve H, Brissot P, Loréal O. Bardou-Jacquet E, et al. Among authors: jouanolle am. Blood Cells Mol Dis. 2011 Dec 15;47(4):243-8. doi: 10.1016/j.bcmd.2011.07.004. Epub 2011 Aug 26. Blood Cells Mol Dis. 2011. PMID: 21871825
Non-HFE hemochromatosis: pathophysiological and diagnostic aspects.
Bardou-Jacquet E, Ben Ali Z, Beaumont-Epinette MP, Loreal O, Jouanolle AM, Brissot P. Bardou-Jacquet E, et al. Among authors: jouanolle am. Clin Res Hepatol Gastroenterol. 2014 Apr;38(2):143-54. doi: 10.1016/j.clinre.2013.11.003. Epub 2013 Dec 8. Clin Res Hepatol Gastroenterol. 2014. PMID: 24321703 Free article. Review.
Hereditary hypotransferrinemia can lead to elevated transferrin saturation and, when associated to HFE or HAMP mutations, to iron overload.
Beaumont-Epinette MP, Delobel JB, Ropert M, Deugnier Y, Loréal O, Jouanolle AM, Brissot P, Bardou-Jacquet E. Beaumont-Epinette MP, et al. Among authors: jouanolle am. Blood Cells Mol Dis. 2015 Feb;54(2):151-4. doi: 10.1016/j.bcmd.2014.11.020. Epub 2014 Nov 26. Blood Cells Mol Dis. 2015. PMID: 25486930 Free article.
78 results