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pro vyhledávání: '"A, Nurden"'
Autor:
Lavenu-Bombled, Cécile, Falaise, Céline, Blandinieres, Adeline, Nurden, Paquita, Alessi, Marie-Christine, Saultier, Paul
Publikováno v:
In Perfectionnement en Pédiatrie March 2024 7(1):48-60
Akademický článek
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Autor:
Koukouritaki, Sevasti B., Thinn, Aye Myat M., Ashworth, Katrina J., Fang, Juan, Slater, Haley S., Du, Lily M., Nguyen, Huong Thi Thu, Pillois, Xavier, Nurden, Alan T., Ng, Christopher J., Di Paola, Jorge, Zhu, Jieqing, Wilcox, David A.
Publikováno v:
In Blood Advances 11 July 2023 7(13):3180-3191
Publikováno v:
In Biomaterials December 2021 279
Autor:
Alan T. Nurden
Publikováno v:
Haematologica, Vol 108, Iss 4 (2023)
Externí odkaz:
https://doaj.org/article/65c2c3b4d6eb44a686594ff6b686de5c
Autor:
Guillet, Benoit, Bayart, Sophie, Pillois, Xavier, Nurden, Paquita, Caen, Jacques P., Nurden, Alan T. *
Publikováno v:
In Journal of Thrombosis and Haemostasis December 2019 17(12):2211-2215
Autor:
Simon Stritt, Paquita Nurden, Alan T. Nurden, Jean-François Schved, Jean-Claude Bordet, Maguelonne Roux, Marie-Christine Alessi, David-Alexandre Trégouët, Taija Mäkinen, Muriel Giansily-Blaizot
Publikováno v:
Haematologica, Vol 108, Iss 3 (2022)
Vascular homeostasis is impaired in various diseases thereby contributing to the progression of their underlying pathologies. The endothelial immediate early gene Apolipoprotein L domain-containing 1 (APOLD1) helps to regulate endothelial function. H
Externí odkaz:
https://doaj.org/article/29cf6506c2be49cd88a04b466c1141d2
Publikováno v:
In Biomaterials February 2019 192:440-460
Autor:
Berrou, Eliane, Soukaseum, Christelle, Favier, Rémi, Adam, Frédéric, Elaib, Ziane, Kauskot, Alexandre, Bordet, Jean-Claude, Ballerini, Paola, Loyau, Stephane, Feng, Miao, Dias, Karine, Muheidli, Abbas, Girault, Stephane, Nurden, Alan T., Turro, Ernest, Ouwehand, Willem H., Denis, Cécile V., Jandrot-Perrus, Martine, Rosa, Jean-Philippe, Nurden, Paquita, Bryckaert, Marijke *
Publikováno v:
In Blood 8 November 2018 132(19):2067-2077
Autor:
Stéphane Loyau Inserm, Dorothée Faille, Philippe Gautier, Paquita Nurden, Martine Jandrot-Perrus, Nadine Ajzenberg
Publikováno v:
Platelets, Vol 32, Iss 5, Pp 705-709 (2021)
Acquired deficiencies in platelet glycoprotein VI are rare and have not been found associated with other defects. Here we report the case of a 64-year old male patient presenting an immune GPVI deficiency associated to a mutation in the alpha-actinin
Externí odkaz:
https://doaj.org/article/2cbf19bd53bb46b98c10c5dbbc6f919f