Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Beatrice Saposnik"'
Autor:
Alain Stepanian, Laurent Mandelbrot, Edith Peynaud-Debayle, Gabriel Baron, Beatrice Saposnik, Maud Simansour, Sophie Gandrille, Dominique de Prost
Publikováno v:
Thrombosis Research. 129:152-157
The endothelial protein C receptor (EPCR) plays a crucial role in the anticoagulant and anti-inflammatory effects of the protein C pathway, whereas its soluble form (sEPCR) exhibits opposite properties. High plasma levels of sEPCR have been observed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4854f88038680f54c40589cabd38b56
https://doi.org/10.1016/j.thromres.2011.07.023
https://doi.org/10.1016/j.thromres.2011.07.023
Autor:
Jean-Luc Reny, Martine Aiach, Joseph Emmerich, Pascale Gaussem, Beatrice Saposnik, Sophie Gandrille
Publikováno v:
Blood. 103(4)
The endothelial cell protein C (PC) receptor (EPCR) facilitates PC activation by the thrombin-thrombomodulin complex. A soluble form of this receptor (sEPCR) found in plasma inhibits both activated PC (aPC) activity and PC activation by competing for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::257cd016a306f8635b3a623c0af4a66f
https://pubmed.ncbi.nlm.nih.gov/14576048
https://pubmed.ncbi.nlm.nih.gov/14576048
Autor:
Odile Fenneteau, Sandrine Elbaz, Valérie Bardet, Nicole Schlegel, Beatrice Saposnik, Sylvie Binard, Bénédicte Gérard, Paquita Nurden
Publikováno v:
Blood. 108:700-700
MYH9-related disorders are autosomal dominant giant platelet syndromes with a wide phenotypic variability known under the following names: May Hegglin Anomaly (MHA), Fechtner Syndrome (FTNS), Epstein Syndrome (EPS), Sebastian Syndrome (SBS) and Alpor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::986e10dd45e1a6839feceb63ac0a28c9
https://doi.org/10.1182/blood.v108.11.700.700
https://doi.org/10.1182/blood.v108.11.700.700
Autor:
Béatrice Saposnik, Sylvie Binard, Odile Fenneteau, Alan Nurden, Paquita Nurden, Marie‐Françoise Hurtaud‐Roux, Nicole Schlegel, the French MYH9 network
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 2, Iss 4, Pp 297-312 (2014)
Abstract MYH9‐Related Disorders are a group of rare autosomal dominant platelet disorders presenting as nonsyndromic forms characterized by macrothrombocytopenia with giant platelets and leukocyte inclusion bodies or as syndromic forms combining th
Externí odkaz:
https://doaj.org/article/f8b0267af6f94c31abf41c0135089159
Autor:
Patrizia Noris, Nicole Schlegel, Catherine Klersy, Paula G. Heller, Elisa Civaschi, Nuria Pujol-Moix, Fabrizio Fabris, Remi Favier, Paolo Gresele, Véronique Latger-Cannard, Adam Cuker, Paquita Nurden, Andreas Greinacher, Marco Cattaneo, Erica De Candia, Alessandro Pecci, Marie-Françoise Hurtaud-Roux, Ana C. Glembotsky, Eduardo Muñiz-Diaz, Maria Luigia Randi, Nathalie Trillot, Loredana Bury, Thomas Lecompte, Caterina Marconi, Anna Savoia, Carlo L. Balduini, Sophie Bayart, Anne Bauters, Schéhérazade Benabdallah-Guedira, Françoise Boehlen, Jeanne-Yvonne Borg, Roberta Bottega, James Bussel, Daniela De Rocco, Emmanuel de Maistre, Michela Faleschini, Emanuela Falcinelli, Silvia Ferrari, Alina Ferster, Tiziana Fierro, Dominique Fleury, Pierre Fontana, Chloé James, Francois Lanza, Véronique Le Cam Duchez, Giuseppe Loffredo, Pamela Magini, Dominique Martin-Coignard, Fanny Menard, Sandra Mercier, Annamaria Mezzasoma, Pietro Minuz, Ilaria Nichele, Lucia D. Notarangelo, Tommaso Pippucci, Gian Marco Podda, Catherine Pouymayou, Agnes Rigouzzo, Bruno Royer, Pierre Sie, Virginie Siguret, Catherine Trichet, Alessandra Tucci, Béatrice Saposnik, Dino Veneri
Publikováno v:
Haematologica, Vol 99, Iss 8 (2014)
Pregnancy in women with inherited thrombocytopenias is a major matter of concern as both the mothers and the newborns are potentially at risk of bleeding. However, medical management of this condition cannot be based on evidence because of the lack o
Externí odkaz:
https://doaj.org/article/7a05c6d478a140358a61baeac4f3925c