Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Marie-Christine Mérour"'
Autor:
Philippe Saliou, Gérald Le Gac, Anne-Yvonne Mercier, Brigitte Chanu, Paul Guéguen, Marie-Christine Mérour, Isabelle Gourlaouen, Sandrine Autret, Cédric Le Maréchal, Karen Rouault, Jean-Baptiste Nousbaum, Claude Férec, Virginie Scotet
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e81128 (2013)
Despite type I haemochromatosis (HC) is mainly associated with the HFE C282Y/C282Y genotype, a second genotype -C282Y/H63D- has mostly been described in other patients. Its association with HC, apart from any associated co-morbid factors, remains unc
Externí odkaz:
https://doaj.org/article/3696df7408e14e219065d8c0cc60737c
Autor:
Khadidja Rebah, Hervé Puy, Katell Peoc'h, Thibaud Lefebvre, Suzanne Assari, Gérald Le Gac, C. L'Hostis, Claude Férec, Dimitri Tchernitchko, Virginie Scotet, Marie-Christine Mérour, Isabelle Gourlaouen
Publikováno v:
Hepatology. 65:1069-1071
Autor:
Kevin Uguen, Virginie Scotet, Claude Férec, Gérald Le Gac, C. L'Hostis, Marie-Christine Mérour, Isabelle Gourlaouen, Tania Cuppens, Chandran Ka
Publikováno v:
American journal of hematology. 92(12)
Autor:
Jean-Baptiste Nousbaum, Claude Férec, Gérald Le Gac, Virginie Scotet, Céline Tripogney, Isabelle Gourlaouen, Marie-Christine Mérour, Brigitte Chanu, Philippe Saliou
Publikováno v:
Annals of hematology. 94(7)
Autor:
Gérald Le Gac, Marie-Christine Mérour, Virginie Scotet, Suzanne Assari, C. L'Hostis, Claude Férec, Isabelle Gourlaouen
Publikováno v:
Transfusion Clinique et Biologique. 24:309
Introduction L’EFS assure la majorite des actes de saignees iteratives proposes dans le cadre d’une hyperferritinemie. Differentes etiologies sont possibles, aux premiers rangs desquelles l’hemochromatose, le syndrome metabolique, la consommati
Autor:
Sandrine Autret, Gérald Le Gac, Claude Férec, Isabelle Gourlaouen, Cédric Le Maréchal, Philippe Saliou, Brigitte Chanu, Jean-Baptiste Nousbaum, Anne-Yvonne Mercier, Marie-Christine Mérour, Karen Rouault, Virginie Scotet, Paul Gueguen
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 12, p e81128 (2013)
PLoS ONE, Vol 8, Iss 12, p e81128 (2013)
Despite type I haemochromatosis (HC) is mainly associated with the HFE C282Y/C282Y genotype, a second genotype -C282Y/H63D- has mostly been described in other patients. Its association with HC, apart from any associated co-morbid factors, remains unc
Autor:
Isabelle Gourlaouen, Virginie Scotet, Marie-Christine Mérour, Suzanne Assari, Claude Férec, Médecins Investigateurs, G. Le Gac, C. L'Hostis
Publikováno v:
Transfusion Clinique et Biologique. 22:216
L’etude EMSAI a ete mise en place a la suite de l’APR-EFS 2010 et de l’arrete du 12 janvier 2009 permettant de proposer une partie des patients atteints d’hemochromatose au don du sang benevole. Deux faits essentiels supportent cette etude :
Autor:
Marie-Christine Mérour, Chandran Ka, Jean-Baptiste Nousbaum, Virginie Scotet, Brigitte Chanu, Catherine Mura, Anne-Yvonne Mercier, Gérald Le Gac, Claude Férec
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, BioMed Central, 2005, 6, pp.24. ⟨10.1186/1471-2350-6-24⟩
BMC Medical Genetics, Vol 6, Iss 1, p 24 (2005)
BMC Medical Genetics, BioMed Central, 2005, 6, pp.24. ⟨10.1186/1471-2350-6-24⟩
BMC Medical Genetics, Vol 6, Iss 1, p 24 (2005)
Background Hereditary hemochromatosis (HH) is a common inherited disorder of iron metabolism in Northern European populations. The discovery of a candidate gene in 1996 (HFE), and of its main mutation (C282Y), has radically altered the way to diagnos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab709bd1e71219a5f76dea1979010d8c
https://doi.org/10.1186/1471-2350-6-24
https://doi.org/10.1186/1471-2350-6-24
Autor:
C. Berquier, Claude Férec, Virginie Scotet, G. Le Gac, Anne-Yvonne Mercier, Marie-Christine Mérour, Philippe Saliou, Brigitte Chanu
Publikováno v:
Transfusion Clinique et Biologique. 20:264
Autor:
Virginie Scotet, Philippe Saliou, Marianne Uguen, Carine L’Hostis, Marie-Christine Merour, Céline Triponey, Brigitte Chanu, Jean-Baptiste Nousbaum, Gerald Le Gac, Claude Ferec
Publikováno v:
BMC Pregnancy and Childbirth, Vol 18, Iss 1, Pp 1-8 (2018)
Abstract Background HFE hemochromatosis is an inborn error of iron metabolism linked to a defect in the regulation of hepcidin synthesis. This autosomal recessive disease typically manifests later in women than men. Although it is commonly stated tha
Externí odkaz:
https://doaj.org/article/9e94fe8d36ec40ceab6896fc13f43ddd