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authFullName_s : Anne-Marie Jouanolle

Iron disorders of genetic origin: a changing world.

Pierre Brissot , Edouard Bardou-Jacquet , Anne-Marie Jouanolle , Olivier Loréal
Trends in Molecular Medicine, 2011, 17 (12), pp.707-13. ⟨10.1016/j.molmed.2011.07.004⟩
Journal articles istex hal-00739428v1
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Monoclonal anti-transferrin antibody: A paradigm for better understanding of iron metabolism.

Martine Ropert , Lénaïck Détivaud , Béatrice Fimbel d'Hauthuille , Mathilde Gautier , Patricia Leroyer et al.
American Journal of Hematology, 2015, 90 (6), pp.E129-E130. ⟨10.1002/ajh.24004⟩
Journal articles hal-01134382v1

Ferroportin diseases: functional studies, a link between genetic and clinical phenotype.

Lénaïck Détivaud , Marie-Laure Island , Anne-Marie Jouanolle , Martine Ropert , Edouard Bardou-Jacquet et al.
Human Mutation, 2013, 34 (11), pp.1529-36. ⟨10.1002/humu.22396⟩
Journal articles istex hal-00876616v1
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Heterozygous Mutations in BMP6 Pro-peptide Lead to Inappropriate Hepcidin Synthesis and Moderate Iron Overload in Humans

Raed Daher , Caroline Kannengiesser , Dounia Houamel , Thibaud Lefebvre , Edouard Bardou-Jacquet et al.
Gastroenterology, 2016, 150 (3), pp.672-683. ⟨10.1053/j.gastro.2015.10.049⟩
Journal articles hal-01231430v1

Iron excess treatable by copper supplementation in acquired aceruloplasminemia: a new form of secondary human iron overload?

Dorothée Videt-Gibou , Serge Belliard , Edouard Bardou-Jacquet , Marie-Bérengère Troadec , Caroline Le Lan et al.
Blood, 2009, 114 (11), pp.2360-1. ⟨10.1182/blood-2009-06-226175⟩
Journal articles inserm-00864014v1
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Hereditary hypotransferrinemia can lead to elevated transferrin saturation and, when associated to HFE or HAMP mutations, to iron overload

Marie-Pascale Beaumont-Epinette , Jean-Bernard Delobel , Martine Ropert , Yves Deugnier , Olivier Loréal et al.
Blood Cells, Molecules and Diseases, 2015, 54 (2), pp.151-154. ⟨10.1016/j.bcmd.2014.11.020⟩
Journal articles hal-01120455v1

Variable age of onset and clinical severity in transferrin receptor 2 related haemochromatosis: novel observations

Edouard Bardou-Jacquet , Severine Cunat , Marie-Pascale Beaumont-Epinette , Caroline Kannengiesser , Xavier Causse et al.
British Journal of Haematology, 2013, 162 (2), pp.278-81. ⟨10.1111/bjh.12350⟩
Journal articles inserm-00836894v1

Molecular diagnosis of genetic iron-overload disorders.

Pierre Brissot , Edouard Bardou-Jacquet , Marie-Bérengère Troadec , Annick Mosser , Marie-Laure Island et al.
Expert Review of Molecular Diagnostics, 2010, 10 (6), pp.755-63. ⟨10.1586/erm.10.55⟩
Journal articles inserm-00863844v1
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Decreased Cardiovascular and Extrahepatic Cancer-Related Mortality In Treated Patients with Mild HFE Hemochromatosis.

Edouard Bardou-Jacquet , Jeff Morcet , Ghislain Manet , Fabrice Lainé , Michèle Perrin et al.
Journal of Hepatology, 2015, 62 (3), pp.682-689. ⟨10.1016/j.jhep.2014.10.025⟩
Journal articles hal-01091479v1

A simple clinical and biological score to promote and enhance Ferroportine disease screening.

Amandine Landemaine , Houda Hamdi-Roze , Véronique Loustaud-Ratti , Xavier Causse , Bernard Drenou et al.
Hepatology, 2017, 66, pp.430A-431A
Journal articles hal-01671423v1

Sex and acquired cofactors determine phenotypes of ferroportin disease.

Caroline Le Lan , Annick Mosser , Martine Ropert , Lénaïck Detivaud , Véronique Loustaud-Ratti et al.
Gastroenterology, 2011, 140 (4), pp.1199-1207.e1-2. ⟨10.1053/j.gastro.2010.12.049⟩
Journal articles inserm-00554693v1

The Monoclonal Anti-Transferrin Antibody Syndrome: A Way for a Better Understanding of Iron Metabolism

Pierre Brissot , Martine Ropert , Lénaïck Détivaud , Beatrice Fimbel d'Hauthuille , Mathilde Gautier et al.
American Journal of Hematology, 2016, 91 (3), pp.E55--E55
Journal articles hal-01300799v1
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Non-HFE hemochromatosis: Pathophysiological and diagnostic aspects.

Edouard Bardou-Jacquet , Zeineb Ben Ali , Marie-Pascale Beaumont-Epinette , Olivier Loréal , Anne-Marie Jouanolle et al.
Clinics and Research in Hepatology and Gastroenterology, 2013, 38 (2), pp.143-154. ⟨10.1016/j.clinre.2013.11.003⟩
Journal articles hal-00925741v1

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.

Edouard Bardou-Jacquet , Marie-Laure Island , Anne-Marie Jouanolle , Lénaïck Détivaud , Nadia Fatih et al.
Blood Cells, Molecules and Diseases, 2011, 47 (4), pp.243-8. ⟨10.1016/j.bcmd.2011.07.004⟩
Journal articles istex hal-00739367v1
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A new mutation in the hepcidin promoter impairs its BMP response and contributes to a severe phenotype in HFE related hemochromatosis.

Marie-Laure Island , Anne-Marie Jouanolle , Annick Mosser , Yves Deugnier , Véronique David et al.
Haematologica, 2009, 94 (5), pp.720-4. ⟨10.3324/haematol.2008.001784⟩
Journal articles inserm-00372237v1
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Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis

Marie de Tayrac , Marie-Paule Roth , Anne-Marie Jouanolle , Hélène Coppin , Gérald Le Gac et al.
Journal of Hepatology, 2015, 62 (3), pp.664-672. ⟨10.1016/j.jhep.2014.10.017⟩
Journal articles hal-01091987v1