Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Claire Briandet"'
Autor:
Thomas Pincez, Helder Fernandes, Thierry Leblanc, Gérard Michel, Vincent Barlogis, Yves Bertrand, Bénédicte Neven, Wadih Abou Chahla, Marlène Pasquet, Corinne Guitton, Aude Marie-Cardine, Isabelle Pellier, Corinne Armari-Alla, Joy Benadiba, Pascale Blouin, Eric Jeziorski, Frédéric Millot, Catherine Paillard, Caroline Thomas, Nathalie Cheikh, Sophie Bayart, Fanny Fouyssac, Christophe Piguet, Marianna Deparis, Claire Briandet, Eric Dore, Capucine Picard, Frédéric Rieux-Laucat, Judith Landman-Parker, Guy Leverger, Nathalie Aladjidi
Publikováno v:
Haematologica, Vol 107, Iss 2 (2021)
Pediatric-onset Evans syndrome (pES) is defined by both immune thrombocytopenic purpura (ITP) and autoimmune hemolytic anemia (AIHA) before the age of 18 years. There have been no comprehensive long-term studies of this rare disease, which can be ass
Externí odkaz:
https://doaj.org/article/2a8e1c08451d410c841e4435da54463d
Autor:
Eric Thebault, Sophie Piperno-Neumann, Diep Tran, Hélène Pacquement, Perrine Marec-Berard, Cyril Lervat, Marie-Pierre Castex, Morgane Cleirec, Emmanuelle Bompas, Jean-Pierre Vannier, Dominique Plantaz, Laure Saumet, Cecile Verite, Olivier Collard, Claire Pluchart, Claire Briandet, Laure Monard, Laurence Brugieres, Marie-Cécile Le Deley, Nathalie Gaspar
Publikováno v:
Cancers, Vol 13, Iss 7, p 1683 (2021)
The purpose was to describe first and subsequent relapses in patients from the OS2006/Sarcome-09 trial, to help future trial design. We prospectively collected and analysed relapse data of all French patients included in the OS2006/Sarcome-09 trial,
Externí odkaz:
https://doaj.org/article/35ea388dec4e4ec2a7c40b1fd4a65427
Autor:
Bernard Aral, Martine Courtois, Sylviane Ragot, Valentin Bourgeois, Elodie Bottolier-Lemallaz, Claire Briandet, François Girodon
Publikováno v:
Haematologica, Vol 103, Iss 8 (2018)
Externí odkaz:
https://doaj.org/article/451d109101804ea2b3325f0250dda862
Autor:
Thomas Pincez, Helder Fernandes, Marlène Pasquet, Wadih Abou Chahla, Jérome Granel, Sébastien Héritier, Mony Fahd, Stéphane Ducassou, Caroline Thomas, Nathalie Garnier, Vincent Barlogis, Eric Jeziorski, Sophie Bayart, Pascal Chastagner, Nathalie Cheikh, Corinne Guitton, Catherine Paillard, Julien Lejeune, Frédéric Millot, Valérie Li‐Thiao Te, Coralie Mallebranche, Isabelle Pellier, Bénédicte Neven, Corinne Armari‐Alla, Liana Carausu, Christophe Piguet, Joy Benadiba, Claire Pluchart, Jean‐Louis Stephan, Marianna Deparis, Claire Briandet, Eric Doré, Aude Marie‐Cardine, Thierry Leblanc, Guy Leverger, Nathalie Aladjidi
Publikováno v:
American Journal of Hematology. 98:857-868
Autor:
Thomas Pincez, Nathalie Aladjidi, Sébastien Héritier, Nathalie Garnier, Mony Fahd, Wadih Abou Chahla, Helder Fernandes, Claire Dichamp, Stéphane Ducassou, Marlène Pasquet, Sophie Bayart, Despina Moshous, Nathalie Cheikh, Catherine Paillard, Dominique Plantaz, Eric Jeziorski, Caroline Thomas, Corinne Guitton, Marianna Deparis, Aude Marie Cardine, Jean-Louis Stephan, Isabelle Pellier, Eric Doré, Joy Benadiba, Claire Pluchart, Claire Briandet, Vincent Barlogis, Guy Leverger, Thierry Leblanc
Publikováno v:
Blood. 140:253-261
Splenectomy is effective in ∼70% to 80% of pediatric chronic immune thrombocytopenia (cITP) cases, and few data exist about it in autoimmune hemolytic anemia (AIHA) and Evans syndrome (ES). Because of the irreversibility of the procedure and the la
Autor:
Coralie Mallebranche, Yves Reguerre, Brice Fresneau, Nicolas Andre, Claire Berger, Claire Briandet, Marie‐Pierre Castex, Anne‐Sophie Defachelles, Cécile Faure‐Conter, Julien Lejeune, Sébastien Klein, Guy Leverger, Aude Marie‐Cardine, Caroline Oudot, Claire Freycon, Stéphanie Proust, Marianne Roumy, Estelle Thebaud, Cécile Verite, Brigitte Lacour, Daniel Orbach
Publikováno v:
Pediatric Blood and Cancer
Pediatric Blood and Cancer, 2022, 69 (12), ⟨10.1002/pbc.30003⟩
Pediatric Blood and Cancer, 2022, 69 (12), ⟨10.1002/pbc.30003⟩
International audience; Introduction: Very rare pediatric tumors (VRTs), defined by an annual incidence ≤2 per million inhabitants, represent a heterogeneous group of cancers. Due to their extremely low incidence, knowledge on these tumors is scant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea7e08bc676b66883288ce4d6b9cfe6b
https://hal.science/hal-04030742
https://hal.science/hal-04030742
Autor:
Arnaud Salmon-Rousseau, Pascal Chavanet, Christelle Auvray, Claire Briandet, Quentin Besset, Claire Desplantes
Publikováno v:
Journal of Bone and Joint Infection. 6:171-178
Bartonella henselae is the bacterial agent responsible for cat scratch disease. This infection is frequently the cause of localized lymphadenitis in children. It is also sometimes responsible for endocarditis, encephalitis, hepatic peliosis and in ra
Autor:
Marina Pierrevelcin, Vincent Flacher, Christopher G. Mueller, Romain Vauchelles, Eric Guerin, Benoît Lhermitte, Erwan Pencreach, Andreas Reisch, Quentin Muller, Layal Doumard, Wacym Boufenghour, Andrey S. Klymchenko, Sophie Foppolo, Charlotte Nazon, Noelle Weingertner, Sophie Martin, Claire Briandet, Véronique Laithier, Antonio Di Marco, Laurent Bund, Adeline Obrecht, Pascal Villa, Monique Dontenwill, Natacha Entz‐Werlé
Publikováno v:
Advanced Healthcare Materials. 11:2200195
Osteosarcoma (OS) is the most common primary bone cancer, where the overall 5-year surviving rate is below 20% in resistant forms. Accelerating cures for those poor outcome patients remains a challenge. Nevertheless, several studies of agents targeti
Autor:
Mickaël Alligon, Nizar Mahlaoui, Virginie Courteille, Laurence Costes, Veronica Afonso, Philippe Randrianomenjanahary, Nathalie de Vergnes, Anja Ranohavimparany, Duy Vo, Inès Hafsa, Perrine Bach, Vincent Benoit, Nicolas Garcelon, Alain Fischer, Wadih Abou-Chahla, Daniel Adoue, Nathalie Aladjidi, Corinne Armari-Alla, Vincent Barlogis, Sophie Bayart, Yves Bertrand, Stéphane Blanche, Damien Bodet, Bernard Bonnotte, Raphaël Borie, Patrick Boutard, David Boutboul, Claire Briandet, Jean-Paul Brion, Jacques Brouard, Liana Carausu, Martin Castelle, Pascal Cathebras, Emilie Catherinot, Nathalie Cheikh, Morgane Cheminant, Sarah Cohen-Beaussant, Thibault Comont, Louis-Jean Couderc, Pierre Cougoul, Gérard Couillault, Lionel Crevon, Elisa Demonchy, Anne Deville, Catherine Devoldere, Eric Dore, Fabienne Dulieu, Isabelle Durieu, Natacha Entz-Werle, Claire Fieschi, Fanny Fouyssac, Pierre Frange, Vincent Gajdos, Lionel Galicier, Virginie Gandemer, Martine Gardembas, Catherine Gaud, Bernard Grosbois, Aurélien Guffroy, Corinne Guitton, Gaëlle Guillerm, Eric Hachulla, Mohamed Hamidou, Sophie Haro, Yves Hatchuel, Olivier Hermine, Cyrille Hoarau, Arnaud Hot, Sébastien Humbert, Arnaud Jaccard, Jean-Philippe Jais, Sarah Jannier, Serge Jacquot, Roland Jaussaud, Pierre-Yves Jeandel, Eric Jeziorski, Kamila Kebaili, Anne-Sophie Korganow, Olivier Lambotte, Fanny Lanternier, Claire Larroche, David Launay, Emmanuelle Le Moigne, Alain Le Quellec, Vincent Le Moing, Yvon Lebranchu, Marc Lecuit, Guillaume Lefèvre, Jean-Daniel Lelièvre, Richard Lemal, Valérie Li-Thiao-Te, Olivier Lortholary, Luminita Luca, Coralie Mallebranche, Marion Malphettes, Aude Marie-Cardine, Nicolas Martin-Silva, Agathe Masseau, Françoise Mazingue, Etienne Merlin, Gérard Michel, Frédéric Millot, Charline Miot, Béatrice Monlibert, Fabrice Monpoux, Despina Moshous, Luc Mouthon, Martine Münzer, Robert Navarro, Bénédicte Neven, Dalila Nouar, Raphaële Nove-Josserand, Eric Oksenhendler, Marie Ouachée-Chardin, Anne Pagnier, Marlène Pasquet, Isabelle Pellier, Yves Perel, Antoinette Perlat, Christophe Piguet, Dominique Plantaz, Sophie Rivière, Pascal Roblot, Pierre-Simon Rohrlich, Bruno Royer, Valéry Salle, Françoise Sarrot-Reynauld, Amélie Servettaz, Jean-Louis Stephan, Nicolas Schleinitz, Harry Sokol, Felipe Suarez, Laure Swiader, Sophie Taque, Caroline Thomas, Olivier Tournilhac, Caroline Thumerelle, Jean-Pierre Vannier, Jean-François Viallard
Publikováno v:
The Journal of allergy and clinical immunology. 149(6)
Noninfectious manifestations-allergy, autoimmunity/inflammation, lymphoproliferation, and malignancies-are known to exist in many primary immunodeficiency diseases (PID) and to participate in prognosis.To obtain a global view on their occurrence, we
Autor:
Eric Jeziorski, Frédéric Millot, Wadih Abou Chahla, Joy Benadiba, Corinne Armari-Alla, Nathalie Aladjidi, Thierry Leblanc, Helder Fernandes, Claire Briandet, Sophie Bayard, Fanny Fouyssac, Thomas Pincez, Christophe Piguet, Yves Bertrand, Marlène Pasquet, Caroline Thomas, Judith Landman-Parker, Isabelle Pellier, Bénédicte Neven, Pascale Blouin, Corinne Guitton, Vincent Barlogis, E. Dore, Catherine Paillard, Aude Marie-Cardine, Gérard Michel, Nathalie Cheikh, Mariana Deparis, Guy Leverger
Publikováno v:
Blood. 136:20-22
Introduction Pediatric-onset Evans syndrome (pES) is defined by the association between immune thrombocytopenic purpura (ITP) and autoimmune hemolytic anemia (AIHA) before the age of 18 years and may be associated to various immunopathological manife