Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Pascale Chrétien"'
Autor:
Che Serguera, Lev Stimmer, Claire-Maelle Fovet, Philippe Horellou, Vanessa Contreras, Nicolas Tchitchek, Julie Massonneau, Carole Leroy, Audrey Perrin, Julien Flament, Philippe Hantraye, Joanna Demilly, Romain Marignier, Pascale Chrétien, Bert‘t Hart, Jean Boutonnat, Clovis Adam, Roger Le-Grand, Kumaran Deiva
Publikováno v:
Journal of Neuroinflammation, Vol 16, Iss 1, Pp 1-14 (2019)
Abstract Background Autoantibodies against myelin oligodendrocyte glycoprotein (anti-MOG-Abs) occur in a majority of children with acquired demyelinating syndromes (ADS) and physiopathology is still under investigation. As cynomolgus macaques immuniz
Externí odkaz:
https://doaj.org/article/e1038794ee40410a885a01b24354e627
Autor:
Philippe Horellou, Aliénor de Chalus, Laetitia Giorgi, Carole Leroy, Pascale Chrétien, Salima Hacein-Bey-Abina, Christine Bourgeois, Xavier Mariette, Ché Serguera, Roger Le Grand, Kumaran Deiva
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
BackgroundMyelin oligodendrocytes glycoprotein (MOG) antibody-associated disease (MOGAD) represent 25% of pediatric acquired demyelinating syndrome (ADS); 40% of them may relapse, mimicking multiple sclerosis (MS), a recurrent and neurodegenerative A
Externí odkaz:
https://doaj.org/article/ad8652ab093d42bda4c0be6345f30bc4
Autor:
Samuel Bitoun, Pierre Roques, Thibaut Larcher, Gaétane Nocturne, Che Serguera, Pascale Chrétien, Guy Serre, Roger Le Grand, Xavier Mariette
Publikováno v:
Frontiers in Immunology, Vol 8 (2017)
ObjectivesAnti-citrullinated peptides antibodies (ACPAs) have high specificity for the diagnosis of rheumatoid arthritis (RA), but their role in the pathophysiology is not fully established. The main genetic risk factor for RA, the shared epitope in
Externí odkaz:
https://doaj.org/article/325e87fa0e134fe7a58c8fd46cf09a6f
Autor:
Aude Gleizes, Clémentine Moulin, Andrada Chiron, Pascale Chrétien, Claire Deback, Salima Hacein-Bey-Abina
Publikováno v:
Revue Francophone des Laboratoires. 2022:66-73
Autor:
Lorraine Flet‐Berliac, Nicolas Tchitchek, Anne Lépine, Anca Florea, Hélène Maurey, Pascale Chrétien, Salima Hacein‐Bey‐Abina, Frederic Villega, Emmanuel Cheuret, Véronique Rogemond, Géraldine Picard, Jérôme Honnorat, Kumaran Deiva
Publikováno v:
Developmental Medicine & Child Neurology. 65:691-700
To study long-term clinical and cognitive outcomes of patients with anti-N-methyl-d-aspartate receptor encephalitis (NMDAR-E), an acute autoimmune neurological disease with severe acute presentations.In this French multicentre retrospective observati
Autor:
Philippe Horellou, Lorraine Flet-Berliac, Carole Leroy, Laetitia Giorgi, Candie Joly, Delphine Desjardins, Pascale Chrétien, Salima Hacein-Bey-Abina, Roger Le Grand, Kumaran Deiva
Publikováno v:
Brain Communications. 5
Acquired demyelinating syndrome associated with myelin oligodendrocyte glycoprotein antibodies, named recently myelin oligodendrocyte glycoprotein-associated disease, represents >27% of this paediatric syndrome. Relapses occur in 40% of them, which m
Autor:
Céline Labeyrie, Andoni Echaniz-Laguna, David Adams, A. Laparra, Clovis Adam, Cécile Cauquil, Pascale Chrétien, S. Henriquez, Olivier Lambotte, S. Hacein-Bey-Abina, P. Catalan, N. Noel, L. Pacoureau, Cécile Goujard
Publikováno v:
La Revue de Médecine Interne. 42:844-854
Resume Les syndromes lymphoproliferatifs (myelomes, maladie de Waldenstrom, leucemie lymphoide chronique, lymphomes) peuvent s’associer a la survenue de neuropathies peripheriques. Le mecanisme est variable : il peut etre dysimmunitaire, associe ou
Autor:
M. Vivinus, Marie-Alexandra Alyanakian, P.A. Apoil, Arnaud Cirée, Anthony Léon, Angélique Grenier, Pascale Nicaise-Roland, Thierry Tabary, Valérie Guérin, Stéphanie Rogeau, Anne Sarrat, Béatrice Uring-Lambert, Martine Pernollet, Lorna Garnier, Pascale Chrétien, Delphine Mariotte, Remy Couderc, Erwan Dumontet, Bertrand Evrard, Benoît Cypriani, Lionel Chollet, Caroline Hémont, Joana Vitte, Céline Beauvillain
Publikováno v:
Annales de Biologie Clinique
Annales de Biologie Clinique, 2020, 78 (3), pp.329-342. ⟨10.1684/abc.2020.1549⟩
Annales de Biologie Clinique, John Libbey Eurotext, 2020, 78 (3), pp.329-342. ⟨10.1684/abc.2020.1549⟩
Annales de Biologie Clinique, 2020, 78 (3), pp.329-342. ⟨10.1684/abc.2020.1549⟩
Annales de Biologie Clinique, John Libbey Eurotext, 2020, 78 (3), pp.329-342. ⟨10.1684/abc.2020.1549⟩
International audience; Accreditation of an in vitro diagnostic assay according to the NHENI/ISO 15189 standard requires to analyze its technical performance before implementation for routine use, and annually when reviewing effectiveness of quality
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4293ecf269b6644ad6f49a0ce50a3cce
https://amu.hal.science/hal-03150166
https://amu.hal.science/hal-03150166
Autor:
Joanna Demilly, Julie Massonneau, Romain Marignier, Roger LeGrand, Jean Boutonnat, Philippe Hantraye, Bert A. 't Hart, Nicolas Tchitchek, Audrey Perrin, Julien Flament, Ché Serguera, Vanessa Contreras, Carole Leroy, Lev Stimmer, Claire-Maëlle Fovet, Pascale Chrétien, Philippe Horellou, Kumaran Deiva, Clovis Adam
Publikováno v:
Journal of Neuroinflammation
Journal of Neuroinflammation, 2019, 16, pp.244. ⟨10.1186/s12974-019-1637-7⟩
Journal of neuroinflammation, 16(1):244. BMC
Journal of Neuroinflammation, BioMed Central, 2019, 16 (1), pp.244. ⟨10.1186/s12974-019-1637-7⟩
Journal of Neuroinflammation, Vol 16, Iss 1, Pp 1-14 (2019)
Journal of Neuroinflammation, 2019, 16, pp.244. ⟨10.1186/s12974-019-1637-7⟩
Journal of neuroinflammation, 16(1):244. BMC
Journal of Neuroinflammation, BioMed Central, 2019, 16 (1), pp.244. ⟨10.1186/s12974-019-1637-7⟩
Journal of Neuroinflammation, Vol 16, Iss 1, Pp 1-14 (2019)
Background Autoantibodies against myelin oligodendrocyte glycoprotein (anti-MOG-Abs) occur in a majority of children with acquired demyelinating syndromes (ADS) and physiopathology is still under investigation. As cynomolgus macaques immunized with r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3a1f4346110a959126490ae7f9924d5
https://cea.hal.science/cea-02397764/document
https://cea.hal.science/cea-02397764/document
Autor:
Pascale Chrétien, Chloé Bost, Lucie Salah, Marie Benaiteau, Valentin Oger, Elise Yazbeck, Catherine Adamsbaum, Kumaran Deiva, Celine Bellesme, Jérôme Honnorat, Hélène Maurey, Caroline Sevin
Publikováno v:
European Journal of Paediatric Neurology
European Journal of Paediatric Neurology, Elsevier, 2020, 26, pp.89-91. ⟨10.1016/j.ejpn.2020.03.002⟩
European Journal of Paediatric Neurology, Elsevier, 2020, 26, pp.89-91. ⟨10.1016/j.ejpn.2020.03.002⟩
Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy is a rare recently defined antibody-mediated encephalitis. Meningo-encephalomyelitis presentation is frequent with lymphocytic pleiocytosis in the cerebro-spinal fluid and brain MRI cla