Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Francoise LeDeist"'
Autor:
Stefan Feske, Claire Hivroz, Gideon Rechavi, Anjana Rao, Capucine Picard, Alexander Papolos, Francoise LeDeist, Frédéric Rieux-Laucat, Kevin Lüthy, Alain Fischer, Christie Ann McCarl, Sara Khalil
Publikováno v:
New England Journal of Medicine. 360:1971-1980
A mutation in ORAI1, the gene encoding the pore-forming subunit of the Ca(2+)-release-activated Ca(2+) (CRAC) channel, abrogates the store-operated entry of Ca(2+) into cells and impairs lymphocyte activation. Stromal interaction molecule 1 (STIM1) i
Publikováno v:
The Journal of Pediatrics. 123:921-928
Major histocompatibility complex class II deficiency (bare lymphocyte syndrome) is a rare primary immunodeficiency disorder characterized by profound defects in human leukocyte antigen class II expression, inconsistent and incomplete expression of hu
Autor:
Stéphane Blanche, Francoise LeDeist, A Fischer, Claude Griscelli, Jean-Louis Stephan, Jean Donadieu
Publikováno v:
Blood. 82:2319-2323
Familial hemophagocytic lymphohistiocytosis (FHL) is a potentially fatal disease characterized by diffuse infiltration by histiocytes and T lymphocytes. Treatment with myelotoxic drugs, such as etoposide, brings about remission in most patients, but
Autor:
Antoine Pariente, Brigitte Bader-Meunier, Brigitte Nelken, Fabrice Monpoux, Corinne Armari-Alla, Francoise Bellmann, Martine Munzer, Capucine Picard, Nathalie Aladjidi, Yves Perel, Arnaud Chaussé, Karima Yacouben, Yves Bertrand, Alain Robert, Francoise LeDeist, Guy Leverger
Publikováno v:
Haematologica. 92(12)
The safety and efficacy of rituximab have been retrospectively assessed in 17 children with Evans syndrome. Patients received 4 or 3 weekly doses of rituximab (375 mg/m(2) per dose) associated with prednisone, alone (14 patients) or associated with o
Autor:
Janbernd Kirschner, Capucine Picard, Bernd H. Belohradsky, Takumi Kawasaki, Jeffery L. Kutok, Jens Röther, Alain Fischer, Anjana Rao, Claire Hivroz, Christie-Ann McCarl, Katrin Plogmann, Michael H. Albert, Gundula Notheis, Alexander Papolos, Stephan Ehl, Francoise LeDeist, Stefan Feske, Sara Khalil
Publikováno v:
Journal of Allergy and Clinical Immunology. 124:1311-1318.e7
Background Defects in the development or activation of T cells result in immunodeficiency associated with severe infections early in life. T-cell activation requires Ca 2+ influx through Ca 2+ -release activated Ca 2+ (CRAC) channels encoded by the g
Autor:
Yves Colin, Y. Perel, Guy Leverger, Gérard Michel, Francoise Ledeist, Geneviève Chêne, Thierry Leblanc, Yves Bertrand, Antoine Pariente, Brigitte Nelken, Nathalie Aladjidi, Brigitte Bader Meunier
Publikováno v:
Blood. 106:1684-1684
Introduction: AIHA is a rare and potentially severe condition in children. To assess the presentation, treatment response and outcome of childhood AIHA, a national multicentric observational study has been started in 2002 in 32 French pediatric hemat
Autor:
Claudia Prinz, Christof von Kalle, Kerstin Schwarzwaelder, Isabelle André-Schmutz, Manfred G. Schmidt, Jingjong Hu, Francoise LeDeist, Alain Fischer, Manuela Wissler, Salima Hacein-Bey-Abina, Alexandrine Garrigue, Marina Cavazzana-Calvo, Hanno Glimm
Publikováno v:
Molecular Therapy. 9:S269
Two children involved in the successful retroviral gene therapy clinical trial of SCID-X1 (2 year survival: 100%, FFTF 60%) developed a malignant T-cell lymphoproliferation 34 months after treatment. In both cases, vector integration into the vicinit
Autor:
Roxane Labrosse, Jane Abou-Diab, Annaliesse Blincoe, Guilhem Cros, Thuy Mai Luu, Colette Deslandres, Martha Dirks, Laura Fazilleau, Philippe Ovetchkine, Pierre Teira, Françoise LeDeist, Isabel Fernandez, Fabien Touzot, Helene Decaluwe, Ugur Halac, Elie Haddad
Publikováno v:
Frontiers in Immunology, Vol 8 (2017)
Chronic granulomatous disease (CGD) is a rare primary immune deficiency caused by mutations in genes coding for components of the nicotinamide adenine dinucleotide phosphate oxidase, characterized by severe and recurrent bacterial and fungal infectio
Externí odkaz:
https://doaj.org/article/5cfd3069f96a4346981cc942c858b320
Akademický článek
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Autor:
Brigitte Bader-Meunier, Nathalie Aladjidi, Françoise Bellmann, Fabrice Monpoux, Brigitte Nelken, Alain Robert, Corinne Armari-Alla, Capucine Picard, Françoise Ledeist, Martine Munzer, Karima Yacouben, Yves Bertrand, Antoine Pariente, Arnaud Chaussé, Yves Perel, Guy Leverger
Publikováno v:
Haematologica, Vol 92, Iss 12 (2007)
The safety and efficacy of rituximab have been retrospectively assessed in 17 children with Evans syndrome. Patients received 4 or 3 weekly doses of rituximab (375 mg/m2 per dose) associated with prednisone, alone (14 patients) or associated with oth
Externí odkaz:
https://doaj.org/article/51be0a6ae8444640b7668d95fed2821e