Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jean-François Castilloux"'
Autor:
Ana-Maria Copaescu, Jean-François Castilloux, Myrna Chababi-Atallah, Christian Sinave, Janie Bertrand
Publikováno v:
Case Reports in Dermatology, Vol 5, Iss 3, Pp 340-346 (2013)
Background: Neutrophilic eccrine hidradenitis (NEH) is a rare condition described mostly in adult patients receiving chemotherapy for acute myelogenous leukemia. When it affects the facial region, it can mimic cellulitis and delay the diagnostic, thu
Externí odkaz:
https://doaj.org/article/53ece3d693d743d7b2dd78a41d8d5ec0
Autor:
Jean-François Castilloux, Julie Gauthier, J. St-Louis, Arnaud Bonnefoy, Stéphanie Cloutier, Catherine Vézina, Christine Demers, Margaret Warner, Christine A. Sabapathy, Evemie Dubé, Janie Charlebois, Georges-Etienne Rivard, Clémence Merlen
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 28(1)
Autor:
Jean-François Castilloux, Evemie Dubé, Christine Demers, Margaret Warner, Jean St-Louis, Karine Doyon, Terry Mizrahi, Arnaud Bonnefoy, Georges-Etienne Rivard, Stéphanie Cloutier
Publikováno v:
Haemophilia. 25:252-257
Acquired haemophilia A (AHA) is a rare autoimmune bleeding disorder caused by neutralizing antibodies against factor VIII (FVIII). Despite significant initial morbidity and mortality, most patients achieve remission with immunosuppressive therapy.Lon
Autor:
Christine Demers, Clémence Merlen, Arnaud Bonnefoy, Christine A. Sabapathy, Jean St-Louis, Evemie Dubé, Stéphanie Cloutier, Georges-Etienne Rivard, Catherine Vezina, Margaret Warner, Jean-François Castilloux, Julie Gauthier
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 27(4)
Autor:
Clémence Merlen, Stéphanie Cloutier, Christine Demers, Evemie Dubé, Jean-François Castilloux, M. Warner, J. St-Louis, Arnaud Bonnefoy, Georges-Etienne Rivard, Catherine Vézina, Christine A. Sabapathy
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 24(2)
Introduction Following a provincial tender, most subjects with haemophilia A in Quebec switched their treatment to a third-generation recombinant B-domain-deleted factor VIII (FVIII). Aim Our objective was to evaluate the incidence of inhibitor devel
Autor:
Alexander Lesokhin, Richard LeBlanc, Meletios A. Dimopoulos, Marcelo Capra, Carmelo Carlo‐Stella, Lionel Karlin, Jean‐Francois Castilloux, Peter Forsberg, Gurdeep Parmar, Axel Tosikyan, Ludek Pour, Vincent Ribrag, Rossella Ribolla, Al‐Ola Abdallah, Nadia Le Roux, Liyan Dong, Helgi van deVelde, Laurent Mayrargue, Lucie Lépine, Sandrine Macé, Philippe Moreau
Publikováno v:
Cancer Medicine, Vol 12, Iss 9, Pp 10254-10266 (2023)
Abstract Background Given the incurable nature of multiple myeloma (MM), efforts are made to improve the efficacy of anti‐CD38 monoclonal antibodies via combinations with other potentially synergistic therapies. This Phase 1/2 trial (NCT03194867) w
Externí odkaz:
https://doaj.org/article/5e8923e3821746dba211ec639b02c19b