Bardou-Jacquet E - Search Results

1

Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis.

de Tayrac M, Roth MP, Jouanolle AM, Coppin H, le Gac G, Piperno A, Férec C, Pelucchi S, Scotet V, Bardou-Jacquet E, Ropert M, Bouvet R, Génin E, Mosser J, Deugnier Y. de Tayrac M, et al. J Hepatol. 2015 Mar;62(3):664-72. doi: 10.1016/j.jhep.2014.10.017. Epub 2014 Oct 18. J Hepatol. 2015. PMID: 25457201 Free article.

2

[Treatment of hemochromatosis and its complications].

Brissot P, Bardou-Jacquet E, Ropert M, Loréal O. Brissot P, et al. Soins. 2007 Jun;(716):40-2. Soins. 2007. PMID: 17718032 French. No abstract available.

3

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.

4

Serum transferrin saturation increase is associated with decrease of antibacterial activity of serum in patients with HFE-related genetic hemochromatosis.

Jolivet-Gougeon A, Loréal O, Ingels A, Danic B, Ropert M, Bardou-Jacquet E, Aqodad N, Aussant-Bertel F, Ferec C, Brissot P. Jolivet-Gougeon A, et al. Am J Gastroenterol. 2008 Oct;103(10):2502-8. doi: 10.1111/j.1572-0241.2008.02036.x. Epub 2008 Aug 5. Am J Gastroenterol. 2008. PMID: 18684194

5

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.

6

[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.

7

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.

8

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

9

Iron disorders of genetic origin: a changing world.

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

10

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. 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

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