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Current approach to hemochromatosis.
Brissot P, Troadec MB, Bardou-Jacquet E, Le Lan C, Jouanolle AM, Deugnier Y, Loréal O. Brissot P, et al. 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.
A new missense mutation in the L ferritin coding sequence associated with elevated levels of glycosylated ferritin in serum and absence of iron overload.
Kannengiesser C, Jouanolle AM, Hetet G, Mosser A, Muzeau F, Henry D, Bardou-Jacquet E, Mornet M, Brissot P, Deugnier Y, Grandchamp B, Beaumont C. Kannengiesser C, et al. Haematologica. 2009 Mar;94(3):335-9. doi: 10.3324/haematol.2008.000125. Epub 2009 Jan 27. Haematologica. 2009. PMID: 19176363 Free PMC article.
[Hyperferritinemia not related to hemochromatosis].
Deugnier Y, Bardou-Jacquet E, Le Lan C, Brissot P. Deugnier Y, et al. Gastroenterol Clin Biol. 2009 Apr;33(4):323-6. doi: 10.1016/j.gcb.2009.02.009. Epub 2009 Mar 24. Gastroenterol Clin Biol. 2009. PMID: 19321282 Free article. French. No abstract available.
[Hereditary iron overload].
Brissot P, Bardou-Jacquet E, Latournerie M, Ropert-Bouchet M, Island ML, Loréal O, Jouanolle AM. Brissot P, et al. Pathol Biol (Paris). 2010 Oct;58(5):316-23. doi: 10.1016/j.patbio.2009.10.011. Epub 2009 Nov 25. Pathol Biol (Paris). 2010. PMID: 19942367 Review. French.
Molecular diagnosis of genetic iron-overload disorders.
Brissot P, Bardou-Jacquet E, Troadec MB, Mosser A, Island ML, Detivaud L, Loréal O, Jouanolle AM. Brissot P, et al. Expert Rev Mol Diagn. 2010 Sep;10(6):755-63. doi: 10.1586/erm.10.55. Expert Rev Mol Diagn. 2010. PMID: 20843199 Review.
Sex and acquired cofactors determine phenotypes of ferroportin disease.
Le Lan C, Mosser A, Ropert M, Detivaud L, Loustaud-Ratti V, Vital-Durand D, Roget L, Bardou-Jacquet E, Turlin B, David V, Loréal O, Deugnier Y, Brissot P, Jouanolle AM. Le Lan C, et al. Gastroenterology. 2011 Apr;140(4):1199-1207.e1-2. doi: 10.1053/j.gastro.2010.12.049. Epub 2011 Jan 1. Gastroenterology. 2011. PMID: 21199650
100 results