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[Diagnosis of iron overload].
Deugnier Y, Gandon Y, Juhel C 4th, Olivié D, Jouanolle AM, Turlin B. Deugnier Y, et al. Among authors: jouanolle am. Rev Prat. 2006 Dec 15;56(19):2118-22. Rev Prat. 2006. PMID: 17416048 French.
[Non-HFE related hereditary iron overload].
Brissot P, Jouanolle AM, Le Lan C, Loreal O, Deugnier Y, David V. Brissot P, et al. Among authors: jouanolle am. Gastroenterol Clin Biol. 2005 May;29(5):565-8. doi: 10.1016/s0399-8320(05)82130-x. Gastroenterol Clin Biol. 2005. PMID: 15980752 Free article. Review. French. No abstract available.
Liver iron is a surrogate marker of severe fibrosis in chronic hepatitis C.
Guyader D, Thirouard AS, Erdtmann L, Rakba N, Jacquelinet S, Danielou H, Perrin M, Jouanolle AM, Brissot P, Deugnier Y. Guyader D, et al. Among authors: jouanolle am. J Hepatol. 2007 Apr;46(4):587-95. doi: 10.1016/j.jhep.2006.09.021. Epub 2006 Nov 10. J Hepatol. 2007. PMID: 17156889
[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.
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. Among authors: jouanolle am. 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
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. Among authors: jouanolle am. 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.
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.
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
78 results