Zobrazeno 1 - 10
of 68
pro vyhledávání: '"Sébastien, Héritier"'
Autor:
Laure Delage, Francesco Carbone, Quentin Riller, Jean-Luc Zachayus, Erwan Kerbellec, Armelle Buzy, Marie-Claude Stolzenberg, Marine Luka, Camille de Cevins, Georges Kalouche, Rémi Favier, Alizée Michel, Sonia Meynier, Aurélien Corneau, Caroline Evrard, Nathalie Neveux, Sébastien Roudières, Brieuc P. Pérot, Mathieu Fusaro, Christelle Lenoir, Olivier Pellé, Mélanie Parisot, Marc Bras, Sébastien Héritier, Guy Leverger, Anne-Sophie Korganow, Capucine Picard, Sylvain Latour, Bénédicte Collet, Alain Fischer, Bénédicte Neven, Aude Magérus, Mickaël Ménager, Benoit Pasquier, Frédéric Rieux-Laucat
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-12 (2023)
Abstract Loss of NBEAL2 function leads to grey platelet syndrome (GPS), a bleeding disorder characterized by macro-thrombocytopenia and α-granule-deficient platelets. A proportion of patients with GPS develop autoimmunity through an unknown mechanis
Externí odkaz:
https://doaj.org/article/250dd0cc900246fba884548604a03ce9
Autor:
Solenne Le Louet, Mohamed-Aziz Barkaoui, Jean Miron, Claire Galambrun, Nathalie Aladjidi, Pascal Chastagner, Kamila Kebaili, Corinne Armari-Alla, Anne Lambilliotte, Julien Lejeune, Despina Moshous, Valeria Della Valle, Chiara Sileo, Hubert Ducou Le Pointe, Jean-François Chateil, Sylvain Renolleau, Jean-Eudes Piloquet, Aurelie Portefaix, Ralph Epaud, Raphaël Chiron, Emmanuelle Bugnet, Gwenaël Lorillon, Abdelatif Tazi, Jean-François Emile, Jean Donadieu, Sébastien Héritier
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Abstract Background Lung involvement in childhood Langerhans cell histiocytosis (LCH) is infrequent and rarely life threatening, but occasionally, severe presentations are observed. Methods Among 1482 children (
Externí odkaz:
https://doaj.org/article/1814abe83c2646b9a45c00fa2c624383
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:
Sébastien Héritier, Zofia Hélias-Rodzewicz, Rikhia Chakraborty, Amel G. Sengal, Christine Bellanné-Chantelot, Caroline Thomas, Anne Moreau, Sylvie Fraitag, Carl E. Allen, Jean Donadieu, Jean-François Emile
Publikováno v:
Molecular Cancer, Vol 16, Iss 1, Pp 1-5 (2017)
Abstract Langerhans cell histiocytosis (LCH) is an inflammatory myeloid neoplasia with constitutive activation of the MAPKinase RAS-RAF-MEK-ERK cell signaling pathway. We analyzed 9 LCH cases without BRAF V600 and MAP2K1 mutations by whole exome sequ
Externí odkaz:
https://doaj.org/article/5fcf34ebe17645f294020d25a4adfd9c
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:
Sarah Melloul, Zofia Hélias-Rodzewicz, Fleur Cohen-Aubart, Frédéric Charlotte, Sylvie Fraitag, Nathalie Terrones, Quentin Riller, Thibaud Chazal, Sébastien Héritier, Anne Moreau, Marianne Kambouchner, Marie Christine Copin, Jean Donadieu, Valérie Taly, Zahir Amoura, Julien Haroche, Jean François Emile
Publikováno v:
Haematologica, Vol 104, Iss 3 (2019)
Externí odkaz:
https://doaj.org/article/50b1d3976ad04387a91debaae302a72e
Autor:
Irena Antonia Ungureanu, Fleur Cohen‐Aubart, Sébastien Héritier, Julien Haroche, Jean Donadieu, Jean‐François Emile
Publikováno v:
Histopathology.
Autor:
Irena Antonia Ungureanu, Fleur Cohen-Aubart, Sébastien Héritier, Sylvie Fraitag, Frédéric Charlotte, Hippolyte Lequain, Zofia Hélias-Rodzewicz, Julien Haroche, Jean Donadieu, Jean-François Emile
Publikováno v:
Virchows Archiv.
Autor:
Laurence Dedeken, Safiatou Diallo, Déborah Salik, Alina Ferster, A. Bott, Margaux Gerbaux, Sébastien Héritier, Chantal Dangoisse
Publikováno v:
Annales de dermatologie et de vénéréologie, 147 (11
Annales de Dermatologie et de Vénéréologie
Annales de Dermatologie et de Vénéréologie, Elsevier Masson, 2020, 147 (11), pp.782-785. ⟨10.1016/j.annder.2020.05.005⟩
Annales de Dermatologie et de Vénéréologie
Annales de Dermatologie et de Vénéréologie, Elsevier Masson, 2020, 147 (11), pp.782-785. ⟨10.1016/j.annder.2020.05.005⟩
Introduction. — The recently identified role of a BRAF somatic mutation in the pathophysiologyof Langerhans cell histiocytosis (LCH) offers new therapeutic options. Herein we describe thecase of a 10-month-old infant with refractory high-risk LCH s
Autor:
Lila Autier, Bertrand Gaymard, Eléonore Bayen, Antoine Del Cul, Fleur Cohen-Aubart, Nadine Martin-Duverneuil, Julien Haroche, Karima Mokhtari, Sébastien Héritier, Jean Donadieu, Khê Hoang-Xuan, Ahmed Idbaih
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical NeurophysiologyReferences. 43(11)
Langerhans cell histiocytosis (LCH) is a rare inflammatory myeloid neoplasm characterized by proliferation of tumor histiocytes that involves multiple organs including central nervous system. The physiopathologic process underlying degenerative neuro