Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Marie‐Christine Merour"'
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
Autor:
Gérald Le Gac, Virginie Scotet, Isabelle Gourlaouen, Carine L'Hostis, Marie‐Christine Merour, Zoubida Karim, Yves Deugnier, Edouard Bardou‐Jacquet, Thibaud Lefebvre, Suzanne Assari, Claude Ferec
Publikováno v:
Alimentary Pharmacology and Therapeuthics
Alimentary Pharmacology and Therapeuthics, 2022, 55 (8), pp.1016-1027. ⟨10.1111/apt.16775⟩
Alimentary Pharmacology and Therapeuthics, 2022, 55 (8), pp.1016-1027. ⟨10.1111/apt.16775⟩
International audience; Background: Venesection is the key therapy in haemochromatosis, but it remains controversial in hyperferritinaemia with moderate iron accumulation. There is substantial evidence that the results of HFE genotyping are routinely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f7875f20d8799b90035d1b871299eb8
https://doi.org/10.1111/apt.16775
https://doi.org/10.1111/apt.16775
Autor:
Jean Baptiste Nousbaum, Gérald Le Gac, Marianne Uguen, Virginie Scotet, Marie Christine Merour, Brigitte Chanu, Claude Férec, C. L'Hostis, Céline Triponey, Philippe Saliou
Publikováno v:
BMC Pregnancy and Childbirth
BMC Pregnancy and Childbirth, BioMed Central, 2018, 18 (1), pp.53. ⟨10.1186/s12884-018-1684-6⟩
BMC Pregnancy and Childbirth, Vol 18, Iss 1, Pp 1-8 (2018)
BMC Pregnancy and Childbirth, BioMed Central, 2018, 18 (1), pp.53. ⟨10.1186/s12884-018-1684-6⟩
BMC Pregnancy and Childbirth, Vol 18, Iss 1, Pp 1-8 (2018)
International audience; 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 comm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b54090c41e934e6d1ccbffd77da28c3c
https://doi.org/10.1186/s12884-018-1684-6
https://doi.org/10.1186/s12884-018-1684-6
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