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E Cadet

Showing results (1-10 of 9) with videos related to

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La Revue De Medecine Interne|December 13, 2005
[Screening for HFE C282Y mutation at birth?]J Rochette, E Cadet
Critical Reviews in Oncology/Hematology|April 23, 2015
The mechanisms of genetically modified vaccinia viruses for the treatment of cancerArtrish Jefferson, Valerie E Cadet, Abigail Hielscher
La Revue De Medecine Interne|April 12, 2005
[Advances in iron metabolism: a transition state]E Cadet, M Gadenne, D Capron, et al.
La Revue De Medecine Interne|May 17, 2005
[Molecular basis in hereditary haemochromatosis]E Cadet, A S Perez, D Capron, et al.
Journal of Medical Genetics|May 3, 2005
Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?E Cadet, D Capron, M Gallet, et al.
Journal of Medical Genetics|October 7, 2004
Recent advances in understanding haemochromatosis: a transition stateK J H Robson, A T Merryweather-Clarke, E Cadet, et al.
Journal of Reproductive Immunology|September 16, 2016
Antibodies directed against annexin A2 and obstetric morbidityV Salle, J Schmidt, A Smail, et al.
Journal of Medical Genetics|January 20, 2004
The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loadingK J Livesey, V L C Wimhurst, K Carter, et al.
Journal of Internal Medicine|January 25, 2003
A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosisE Cadet, D Capron, A S Perez, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
La Revue De Medecine Interne|December 13, 2005
[Screening for HFE C282Y mutation at birth?]J Rochette, E Cadet
Critical Reviews in Oncology/Hematology|April 23, 2015
The mechanisms of genetically modified vaccinia viruses for the treatment of cancerArtrish Jefferson, Valerie E Cadet, Abigail Hielscher
La Revue De Medecine Interne|April 12, 2005
[Advances in iron metabolism: a transition state]E Cadet, M Gadenne, D Capron, et al.
La Revue De Medecine Interne|May 17, 2005
[Molecular basis in hereditary haemochromatosis]E Cadet, A S Perez, D Capron, et al.
Journal of Medical Genetics|May 3, 2005
Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?E Cadet, D Capron, M Gallet, et al.
Journal of Medical Genetics|October 7, 2004
Recent advances in understanding haemochromatosis: a transition stateK J H Robson, A T Merryweather-Clarke, E Cadet, et al.
Journal of Reproductive Immunology|September 16, 2016
Antibodies directed against annexin A2 and obstetric morbidityV Salle, J Schmidt, A Smail, et al.
Journal of Medical Genetics|January 20, 2004
The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loadingK J Livesey, V L C Wimhurst, K Carter, et al.
Journal of Internal Medicine|January 25, 2003
A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosisE Cadet, D Capron, A S Perez, et al.
Pageof 1