Anne-marie Jouanolle

Rennes, 35000, France

Last Updated: 09/26/2026

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Found 10 publications

Rare HFE variants are the most frequent cause of hemochromatosis in non-c282y homozygous patients with hemochromatosis.

Rare HFE variants are the most frequent cause of hemochromatosis in non-c282y homozygous patients with hemochromatosis.

Journal: American journal of hematology

Published: May 06, 2016

Monoclonal anti-transferrin antibody: a paradigm for better understanding of iron metabolism.

Monoclonal anti-transferrin antibody: a paradigm for better understanding of iron metabolism.

Journal: American journal of hematology

Published: March 04, 2015

Heterozygous Mutations in BMP6 Pro-peptide Lead to Inappropriate Hepcidin Synthesis and Moderate Iron Overload in Humans.

Heterozygous Mutations in BMP6 Pro-peptide Lead to Inappropriate Hepcidin Synthesis and Moderate Iron Overload in Humans.

Journal: Gastroenterology

Published: October 09, 2014

Hereditary hypotransferrinemia can lead to elevated transferrin saturation and, when associated to HFE or HAMP mutations, to iron overload.

Hereditary hypotransferrinemia can lead to elevated transferrin saturation and, when associated to HFE or HAMP mutations, to iron overload.

Journal: Blood cells, molecules & diseases

Published: September 07, 2014

Decreased cardiovascular and extrahepatic cancer-related mortality in treated patients with mild HFE hemochromatosis.

Decreased cardiovascular and extrahepatic cancer-related mortality in treated patients with mild HFE hemochromatosis.

Journal: Journal of hepatology

Published: April 29, 2014

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

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

Journal: Journal of hepatology

Published: February 25, 2014

Non-HFE hemochromatosis: pathophysiological and diagnostic aspects.

Non-HFE hemochromatosis: pathophysiological and diagnostic aspects.

Journal: Clinics and research in hepatology and gastroenterology

Published: August 20, 2013

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

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

Journal: British journal of haematology

Published: April 23, 2013

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

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

Journal: Human mutation

Published: April 04, 2013

Molecular diagnosis of HFE mutations in routine laboratories. Results of a survey from reference laboratories in France

Molecular diagnosis of HFE mutations in routine laboratories. Results of a survey from reference laboratories in France

Journal: Annales de biologie clinique

Published: May 09, 2012

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Last Updated: 09/26/2026