Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Marie, Dreyfus"'
Autor:
Awa O.T. Fall, Valérie Proulle, Abibatou Sall, Alassane Mbaye, Pape Samba Ba, Maboury Diao, Moussa Seck, Macoura Gadji, Sara B. Gning, Saliou Diop, Tandakha N.D. Dièye, Blaise Félix Faye, Doudou Thiam, Marie Dreyfus
Publikováno v:
Clinical Medicine Insights: Blood Disorders, Vol 2014, Iss 7, Pp 1-6 (2014)
Externí odkaz:
https://doaj.org/article/b7f468732b1241db9cea01df5f8a3391
Autor:
Hanitra Randrianaivo‐Ranjatoelina, Christian Gachet, Arnaud Dupuis, Mathieu Fiore, Marie‐Line Jacquemont, Cécile Lavenu-Bombled, Marie Dreyfus, François Lanza, Céline De Thoré, Renhao Li, Marie-Jeanne Baas
Publikováno v:
Br J Haematol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bec71f4a3eae3e0de0616b9cb0690b5
https://europepmc.org/articles/PMC7263367/
https://europepmc.org/articles/PMC7263367/
Autor:
Edith Fressinaud, Marie Dreyfus, Corinne Guitton, Claudine Caron, Celine Desconclois, Marie-Jeanne Baas, Arnaud Dupuis, Cécile Lavenu-Bombled, François Lanza, Renhao Li, Christian Gachet
Publikováno v:
Thrombosis and haemostasis. 116(6)
SummaryInteraction between von Willebrand factor (VWF) and platelet GPIbα is required for primary haemostasis. Lack or loss-of-function in the ligand-receptor pair results in bleeding complications. Paradoxically, gain-of-function mutations in VWF o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe3cd30f0b25f98a74c3c9271055eec1
https://pubmed.ncbi.nlm.nih.gov/27683759
https://pubmed.ncbi.nlm.nih.gov/27683759
Autor:
Marie Dreyfus, David Adams, Denis Ducreux, Christian Denier, Gérard Tertian, Ombeline Fagniez
Publikováno v:
Journal of the Neurological Sciences. 304:87-92
Hematological disorders (HD) have been estimated to implicate approximately 1% of patients with arterial ischemic stroke. However, previously published studies are mostly retrospective or based on case reports or small series in selected young patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c7507de7e584b5cc405889e81055863
https://doi.org/10.1016/j.jns.2011.02.004
https://doi.org/10.1016/j.jns.2011.02.004
Autor:
Jean-François Delfraissy, Cécile Goujard, Tewfik Boutekedjiret, Philippe Le Bras, Thierry Lambert, Olivier Lambotte, Marie Dreyfus, Benoît Guillet, Justine Dautremer, Rami Kotb
Publikováno v:
Journal of the American Geriatrics Society. 55:1682-1685
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b7021e1915944651096f785e368f028
https://doi.org/10.1111/j.1532-5415.2007.01323.x
https://doi.org/10.1111/j.1532-5415.2007.01323.x
Autor:
Nathalie Martins, Peggy Sirvain-Trukniewicz, Margaret L. Rand, Marc Trossaert, Jenny Goudemand, Paquita Nurden, Mathieu Fiore, Schéhérazade Benabdallah‐Guerida, Roseline d Oiron, Pierre Sié, Marie-Christine Alessi, Juan Pablo Fronthroth, Mathias Canault, Lorenzo Alberio, Christine Vinciguerra, Mathilde Fretigny, Diane J. Nugent, Mariana Bonduel, Alan T. Nurden, Claude Negrier, Véronique Latger-Cannard, Xavier Pillois, Arnaud Couloux, Yves Gruel, Roland Heilig, Marie Dreyfus
Publikováno v:
Human Mutation
Human Mutation, Wiley, 2015, 36 (5), pp.548-561. ⟨10.1002/humu.22776⟩
Nurden, Alan T; Pillois, Xavier; Fiore, Mathieu; Alessi, Marie-Christine; Bonduel, Mariana; Dreyfus, Marie; Goudemand, Jenny; Gruel, Yves; Benabdallah-Guerida, Schéhérazade; Latger-Cannard, Véronique; Négrier, Claude; Nugent, Diane; d'Oiron, Roseline; Rand, Margaret L; Sié, Pierre; Trossaert, Marc; Alberio, Lorenzo; Martins, Nathalie; Sirvain-Trukniewicz, Peggy; Couloux, Arnaud; ... (2015). Expanding the Mutation Spectrum Affecting αIIbβ3 Integrin in Glanzmann Thrombasthenia: Screening of the ITGA2B and ITGB3 Genes in a Large International Cohort. Human mutation, 36(5), pp. 548-561. Wiley-Blackwell 10.1002/humu.22776
Human Mutation, Wiley, 2015, 36 (5), pp.548-561. 〈10.1002/humu.22776〉
Human Mutation, 2015, 36 (5), pp.548-561. ⟨10.1002/humu.22776⟩
Human Mutation, Wiley, 2015, 36 (5), pp.548-561. ⟨10.1002/humu.22776⟩
Nurden, Alan T; Pillois, Xavier; Fiore, Mathieu; Alessi, Marie-Christine; Bonduel, Mariana; Dreyfus, Marie; Goudemand, Jenny; Gruel, Yves; Benabdallah-Guerida, Schéhérazade; Latger-Cannard, Véronique; Négrier, Claude; Nugent, Diane; d'Oiron, Roseline; Rand, Margaret L; Sié, Pierre; Trossaert, Marc; Alberio, Lorenzo; Martins, Nathalie; Sirvain-Trukniewicz, Peggy; Couloux, Arnaud; ... (2015). Expanding the Mutation Spectrum Affecting αIIbβ3 Integrin in Glanzmann Thrombasthenia: Screening of the ITGA2B and ITGB3 Genes in a Large International Cohort. Human mutation, 36(5), pp. 548-561. Wiley-Blackwell 10.1002/humu.22776
Human Mutation, Wiley, 2015, 36 (5), pp.548-561. 〈10.1002/humu.22776〉
Human Mutation, 2015, 36 (5), pp.548-561. ⟨10.1002/humu.22776⟩
We report the largest international study on Glanzmann thrombasthenia (GT), an inherited bleeding disorder where defects of the ITGA2B and ITGB3 genes cause quantitative or qualitative defects of the αIIbβ3 integrin, a key mediator of platelet aggr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::358ff25c74615094c6d807e42ca946e2
Autor:
Caroline Pinganaud, Marie Dreyfus, Gil Tchernia, Olivier Lambotte, Jean-François Delfraissy, Cécile Goujard, Rami Kotb, Catherine Trichet
Publikováno v:
European Journal of Haematology. 75:60-64
UNLABELLED Treatment of auto-immune cytopenia refractory to front line therapy with intravenous immunoglobulins and steroids is a matter of concern. We assessed the efficacy and safety of mycophenolate mofetil in a prospective open preliminary study.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ac12379ef51d2311df2f0e57d245f87
https://doi.org/10.1111/j.1600-0609.2005.00437.x
https://doi.org/10.1111/j.1600-0609.2005.00437.x
Publikováno v:
Blood Coagulation & Fibrinolysis. 14:505-511
To improve the standardization of the factor VII clotting activity (FVII:C) assay in patients treated with recombinant activated factor VII (rFVIIa), we conducted a multicentre study on plasma samples from four patients with haemophilia A, before and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1900ea2f6a4ef02216a545a687ad8f35
https://doi.org/10.1097/00001721-200307000-00013
https://doi.org/10.1097/00001721-200307000-00013
Autor:
Marie Dreyfus, Valérie Proulle, Fakhri Mahdi, Alvin H. Schmaier, Yelena Krijanovski, Werner Müller-Esterl
Publikováno v:
Blood. 101:4430-4436
A 6-year-old male with vertebral-basilar artery thrombosis was recognized to have high-molecular-weight kininogen (HK) deficiency. The propositus had no HK procoagulant activity and antigen (< 1%). Using monoclonal antibodies (Mabs) to kininogen doma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::132976b1dab19a5e92e859250fde72c6
https://doi.org/10.1182/blood-2002-11-3329
https://doi.org/10.1182/blood-2002-11-3329
Autor:
Florence Mathonnet, Jean-Claude Alvarez, Laurent Guillon, Hélène Détruit, Guy-Michel Mazmanian, Philippe de Mazancourt, Marie Dreyfus, Yves Giudicelli
Publikováno v:
Blood Coagulation & Fibrinolysis. 14:293-298
A fibrinogen variant was identified in a pregnant patient with disseminated intravascular coagulation and abruptio placentae. This dysfibrinogen was also found in four asymptomatic members of the patient's family. Coagulation studies showed prolongat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::903766e9b9289cad6243e0cabb676010
https://doi.org/10.1097/01.mbc.0000061286.28953.65
https://doi.org/10.1097/01.mbc.0000061286.28953.65