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Iron disorders of genetic origin: a changing world.
Pierre Brissot
,
Edouard Bardou-Jacquet
,
Anne-Marie Jouanolle
,
Olivier Loréal
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.
Journal articles
hal-01134382v1
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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.
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.
Journal articles
hal-01231430v1
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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.
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.
Journal articles
hal-01120455v1
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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.
Journal articles
inserm-00836894v1
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Molecular diagnosis of genetic iron-overload disorders.
Pierre Brissot
,
Edouard Bardou-Jacquet
,
Marie-Bérengère Troadec
,
Annick Mosser
,
Marie-Laure Island
et al.
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 articles
hal-01091479v1
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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
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Sex and acquired cofactors determine phenotypes of ferroportin disease.
Caroline Le Lan
,
Annick Mosser
,
Martine Ropert
,
Lénaïck Detivaud
,
Véronique Loustaud-Ratti
et al.
Journal articles
inserm-00554693v1
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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.
Journal articles
hal-00925741v1
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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.
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.
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 articles
hal-01091987v1
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