Comprehensive functional annotation of 18 missense mutations found in suspected hemochromatosis type 4 patients
Callebaut, Isabelle, Joubrel, Rozenn, Pissard, Serge, Kannengiesser, Caroline, Gérolami, Victoria, Ged, Cécile, Cadet, Estelle, Cartault, François, Ka, Chandran, Gourlaouen, Isabelle, Gourhant, Lénaick, Oudin, Claire, Goossens, Michel, Grandchamp, Bernard, De Verneuil, Hubert, Rochette, Jacques, Férec, Claude, Le Gac, Gérald
Published in Human molecular genetics (01.09.2014)
Published in Human molecular genetics (01.09.2014)
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The mechanisms of genetically modified vaccinia viruses for the treatment of cancer
Jefferson, Artrish, Cadet, Valerie E, Hielscher, Abigail
Published in Critical reviews in oncology/hematology (01.09.2015)
Published in Critical reviews in oncology/hematology (01.09.2015)
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Journal Article
Recent advances in understanding haemochromatosis: a transition state
Robson, K J H, Merryweather-Clarke, A T, Cadet, E, Viprakasit, V, Zaahl, M G, Pointon, J J, Weatherall, D J, Rochette, J
Published in Journal of Medical Genetics (01.10.2004)
Published in Journal of Medical Genetics (01.10.2004)
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Book Review
Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?
Cadet, E, Capron, D, Gallet, M, Omanga-Léké, M-L, Boutignon, H, Julier, C, Robson, K J H, Rochette, J
Published in Journal of medical genetics (01.05.2005)
Published in Journal of medical genetics (01.05.2005)
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Journal Article
The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading
Livesey, K J, Wimhurst, V L C, Carter, K, Worwood, M, Cadet, E, Rochette, J, Roberts, A G, Pointon, J J, Merryweather-Clarke, A T, Bassett, M L, Jouanolle, A-M, Mosser, A, David, V, Poulton, J, Robson, K J H
Published in Journal of medical genetics (01.01.2004)
Published in Journal of medical genetics (01.01.2004)
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Journal Article
In-Office Needle Arthroscopy: A Systematic Review of Indications and Clinical Utility
Zhang, Kailai, Crum, Raphael J., Samuelsson, Kristian, Cadet, Edwin, Ayeni, Olufemi Rolland, de SA, Darren
Published in Arthroscopy (01.09.2019)
Published in Arthroscopy (01.09.2019)
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Journal Article
A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosis
Cadet, E., Capron, D., Perez, A. S., Crépin, S. N., Arlot, S., Ducroix, J.‐P., Dautréaux, M., Fardellone, P., Leflon, P., Merryweather‐Clarke, A. T., Livesey, K. J., Pointon, J. J., Rose, P., Harcourt, J., Emery, J., Sueur, J. M., Feyt, R., Robson, K. J. H., Rochette, J.
Published in Journal of internal medicine (01.02.2003)
Published in Journal of internal medicine (01.02.2003)
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Closure, Anticoagulation, or Antiplatelet Therapy for Cryptogenic Stroke With Patent Foramen Ovale: Systematic Review of Randomized Trials, Sequential Meta-Analysis, and New Insights From the CLOSE Study
Turc, Guillaume, Calvet, David, Guérin, Patrice, Sroussi, Marjorie, Chatellier, Gilles, Mas, Jean-Louis
Published in Journal of the American Heart Association (17.06.2018)
Published in Journal of the American Heart Association (17.06.2018)
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Journal Article
Données récentes sur le métabolisme du fer : un état de transition
Cadet, E., Gadenne, M., Capron, D., Rochette, J.
Published in La revue de medecine interne (01.04.2005)
Published in La revue de medecine interne (01.04.2005)
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Journal Article
Bases moléculaires des hémochromatoses génétiques
Cadet, E., Perez, A.S., Capron, D., Rochette, J.
Published in La revue de medecine interne (01.05.2005)
Published in La revue de medecine interne (01.05.2005)
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Journal Article
Proximal humerus and humeral shaft nonunions
Cadet, Edwin R, Yin, Bob, Schulz, Brian, Ahmad, Christopher S, Rosenwasser, Melvin P
Published in Journal of the American Academy of Orthopaedic Surgeons (01.09.2013)
Published in Journal of the American Academy of Orthopaedic Surgeons (01.09.2013)
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Journal Article
Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis
Merryweather-Clarke, Alison T., Cadet, Estelle, Bomford, Adrian, Capron, Dominique, Viprakasit, Vip, Miller, Anne, McHugh, Paddy J., Chapman, Roger W., Pointon, Jennifer J., Wimhurst, Victoria L.C., Livesey, Karen J., Tanphaichitr, Voravarn, Rochette, Jacques, Robson, Kathryn J.H.
Published in Human molecular genetics (01.09.2003)
Published in Human molecular genetics (01.09.2003)
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Journal Article
Iron overload in HFE C282Y heterozygotes at first genetic testing: a strategy for identifying rare HFE variants
AGUILAR-MARTINEZ, Patricia, GRANDCHAMP, Bernard, CUNAT, Séverine, CADET, Estelle, BLANC, François, NOURRIT, Marlène, LASSOUED, Kaiss, SCHVED, Jean-François, ROCHETTE, Jacques
Published in Haematologica (Roma) (01.04.2011)
Published in Haematologica (Roma) (01.04.2011)
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Journal Article
Novel mutation in ferroportin 1 gene is associated with autosomal dominant iron overload
Jouanolle, Anne-Marie, Douabin-Gicquel, Véronique, Halimi, Chantal, Loréal, Olivier, Fergelot, Patricia, Delacour, Thierry, de Lajarte-Thirouard, Anne-Sophie, Turlin, Bruno, Le Gall, Jean-Yves, Cadet, Estelle, Rochette, Jacques, David, Véronique, Brissot, Pierre
Published in Journal of hepatology (01.08.2003)
Published in Journal of hepatology (01.08.2003)
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Journal Article
Des génotypes rouillés
CADET, Estelle, WARIN, Renaud, PEREZ, Anne-Sophie, CAPRON, Dominique, ROCHETTE, Jacques
Published in M.S. Médecine sciences (2001)
Published in M.S. Médecine sciences (2001)
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