Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Celine Bellesme"'
Autor:
Manoelle Kossorotoff, Fernando Pico, Diana Rodriguez, David Germanaud, Michael Obadia, Julia Devianne, Yannick Béjot, Christian Denier, Nicolas Legris, Celine Bellesme, Céline Guidoux, Philippe Tuppin, Isabelle Crassard
Publikováno v:
Neurology
Background and ObjectivesWe aimed to analyze the epidemiologic, clinical, and paraclinical features of adolescents with cerebral venous thrombosis (CVT) and its therapeutic management and outcome.MethodsThis multicenter retrospective cohort included
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab8de0feaad7aa022e1bfdb38a9e0f9b
https://europepmc.org/articles/PMC8601207/
https://europepmc.org/articles/PMC8601207/
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
Autor:
Melanie Le Sauter, Caroline Sevin, Anca Florea, Kumaran Deiva, Celine Bellesme, Hélène Maurey
Publikováno v:
Developmental medicine and child neurologyReferences. 62(2)
To evaluate fatigue, depression, and quality of life (QoL) of children with multiple sclerosis and compare to other acute demyelinating syndromes (ADS).Children followed in the National Referral Centre of rare inflammatory brain and spinal diseases w
Autor:
Marie-Anne Colle, Dolan Sondhi, Sabata Martino, Michel Zerah, Clémence Castaignède Lalande, Patrick Aubourg, Monique Piraud, Caroline Sevin, Célia Couzinié, Oumeya Adjali, Carine Cormary, Thomas Baugnon, Philippe Mouiller, Ronald G. Crystal, Mark M. Souweidane, Nathalie Cartier, Thomas Roujeau, Celine Bellesme, Catherine Adamsbaum
Publikováno v:
Molecular Genetics and Metabolism
14. Annual WORLD Symposium (WORLD Symposium 2018)
14. Annual WORLD Symposium (WORLD Symposium 2018), Feb 2018, San Diego, Californie, United States. 173 p., ⟨10.1016/j.ymgme.2017.12.352⟩
14. Annual WORLD Symposium (WORLD Symposium 2018)
14. Annual WORLD Symposium (WORLD Symposium 2018), Feb 2018, San Diego, Californie, United States. 173 p., ⟨10.1016/j.ymgme.2017.12.352⟩
Part of special issue: Lysosome (2018); International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42278771e5a3380c405c1c4ce45b9d5c
https://hal.inrae.fr/hal-02737676
https://hal.inrae.fr/hal-02737676
Autor:
Gilles Edan, Nicolas Collongues, Frédéric Blanc, Eloi Magnin, Marc Bataillard, Mickael Cohen, Thierry Levade, David Brassat, Jean-Philippe Neau, Patrizia Amati-Bonneau, Xavier Ayrignac, Maurice Giroud, Patrick Vermersch, Eric Berger, Cyril Goizet, Celine Bellesme, Clarisse Carra-Dalliere, Jean Louis Devoize, Christophe Verny, Anne Marie Guennoc, Pierre Labauge, Marc Debouverie, Pierre Clavelou, Thibault Moreau, Jean Pelletier, Laurent Magy, Bruno Brochet, Christian Denier, Jean-Philippe Camdessanché, Sandrine Wiertlewski, Nicolas Menjot de Champfleur, Jean-Christophe Ouallet, Gilles Defer, Frédérique Taithe, Elsa Kaphan, Nathalie Derache, Françoise Durand-Dubief, Michel Clanet, Sandra Vukusic, Christine Lebrun-Frenay, Stéphane Mathis, Olivier Outteryck, Bertrand Audoin, Lucie Guyant-Maréchal, Odile Boespflug Tanguy, Elisabeth Tournier-Lasserve, Didier Hannequin, Hélène Zéphir, Jean-Baptiste Chanson, Emmanuelle Le Page, Patrick Aubourg, Sophie Pittion, Jérôme De Seze, Imen Dorboz, Véronique Deburghgraeve, Giovanni Castelnovo, Dominique Bonneau, Julien Masliah-Planchon, David-Axel Laplaud
Publikováno v:
Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2015, 138 (Pt 2), pp.284-92. ⟨10.1093/brain/awu353⟩
Brain-A Journal of Neurology, 2015, 138 (Pt 2), pp.284-92. ⟨10.1093/brain/awu353⟩
Brain-A Journal of Neurology, Oxford University Press (OUP), 2015, 138 (Pt 2), pp.284-92. 〈10.1093/brain/awu353〉
Brain-A Journal of Neurology, Oxford University Press (OUP), 2015, 138 (Pt 2), pp.284-92. ⟨10.1093/brain/awu353⟩
Brain-A Journal of Neurology, 2015, 138 (Pt 2), pp.284-92. ⟨10.1093/brain/awu353⟩
Brain-A Journal of Neurology, Oxford University Press (OUP), 2015, 138 (Pt 2), pp.284-92. 〈10.1093/brain/awu353〉
International audience; Inherited white matter diseases are rare and heterogeneous disorders usually encountered in infancy. Adult-onset forms are increasingly recognized. Our objectives were to determine relative frequencies of genetic leukoencephal
Autor:
Christophe Verny, Pierre Labauge, Clarisse Scherer, Clarisse Carra-Dalliere, Nicolas Menjot de Champfleur, Xavier Ayrignac, Celine Bellesme
Publikováno v:
Clinical Neurology and Neurosurgery. 115:1906-1907