Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Anne, Rolland"'
Publikováno v:
Building Healthy Academic Communities Journal, Vol 7, Iss 2, Pp 25-39 (2023)
Background: Military Veterans (MVs) face unique challenges that are important to recognize when building supportive academic environments. There is a need to broaden our understanding of the diverse student population within academia, requiring us to
Externí odkaz:
https://doaj.org/article/98077dbc19b3473f9c9cfb7b064dd5f7
Autor:
Manoëlle, Kossorotoff, Basile, Kerleroux, Grégoire, Boulouis, Béatrice, Husson, Kim, Tran Dong, François, Eugene, Lena, Damaj, Augustin, Ozanne, Céline, Bellesme, Anne, Rolland, Romain, Bourcier, Aude, Triquenot-Bagan, Gaultier, Marnat, Jean-Philippe, Neau, Sylvie, Joriot, Alexandra, Perez, Maud, Guillen, Maximilien, Perivier, Frederique, Audic, Jean François, Hak, Christian, Denier, Olivier, Naggara, Denis, Herbreteaux
Publikováno v:
JAMA network open. 5(9)
ImportanceThere is to date limited evidence that revascularization strategies are associated with improved functional outcome in children with acute ischemic stroke (AIS).ObjectivesTo report clinical outcomes and provide estimates of revascularizatio
Autor:
Myriam Vezain, Christel Thauvin-Robinet, Yoann Vial, Sophie Coutant, Séverine Drunat, Jon Andoni Urtizberea, Anne Rolland, Agnès Jacquin-Piques, Séverine Fehrenbach, Gaël Nicolas, François Lecoquierre, Pascale Saugier-Veber
Publikováno v:
Human Genetics
Human Genetics, 2022, ⟨10.1007/s00439-017-1811-x⟩
Human Genetics, 2022, ⟨10.1007/s00439-017-1811-x⟩
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder resulting from biallelic alterations of the SMN1 gene: deletion, gene conversion or, in rare cases, intragenic variants. The disease severity is mainly influenced by the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3efba974188d600cf82195d253513950
https://doi.org/10.21203/rs.3.rs-1666246/v1
https://doi.org/10.21203/rs.3.rs-1666246/v1
Autor:
Claire Bar, Delphine Breuillard, Mathieu Kuchenbuch, Mélanie Jennesson, Gwenaël Le Guyader, Hervé Isnard, Anne Rolland, Diane Doummar, Joel Fluss, Alexandra Afenjar, Patrick Berquin, Anne De Saint Martin, Sophie Dupont, Alice Goldenberg, Damien Lederer, Gaétan Lesca, Hélène Maurey, Pierre Meyer, Cyril Mignot, Anca Nica, Sylvie Odent, Alice Poisson, Emmanuel Scalais, Tayeb Sekhara, Pascal Vrielynck, Giulia Barcia, Rima Nabbout
Publikováno v:
Epilepsy & Behavior
Epilepsy & Behavior, [San Diego CA]: Elsevier B.V., 2022, 126, pp.108471. ⟨10.1016/j.yebeh.2021.108471⟩
Epilepsy & Behavior, 2022, 126, pp.108471. ⟨10.1016/j.yebeh.2021.108471⟩
Epilepsy & Behavior, [San Diego CA]: Elsevier B.V., 2022, 126, pp.108471. ⟨10.1016/j.yebeh.2021.108471⟩
Epilepsy & Behavior, 2022, 126, pp.108471. ⟨10.1016/j.yebeh.2021.108471⟩
International audience; Aim: KCNB1 encephalopathy encompasses a broad phenotypic spectrum associating intellectual disability, behavioral disturbances, and epilepsies of various severity. Using standardized parental questionnaires, we aimed to captur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96f727a2584974e9f56a051aa8168a13
https://hal.archives-ouvertes.fr/hal-03485808
https://hal.archives-ouvertes.fr/hal-03485808
Publikováno v:
Des guerres civiles du xvie siècle à nos jours ISBN: 9782753586253
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae19a989127ab13764360c776505ebb5
https://doi.org/10.4000/books.pur.185316
https://doi.org/10.4000/books.pur.185316
Autor:
Anne Rolland-Boulestreau
Publikováno v:
Cessez-le-feu, cesser les combats ? ISBN: 9782757437193
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b7e06ad7d24974cb98a0f7982a4e82a
https://doi.org/10.4000/books.septentrion.136883
https://doi.org/10.4000/books.septentrion.136883
Publikováno v:
Dictionnaire des conventionnels
Dictionnaire des conventionnels, Centre international d'étude du XVIIIe siècle Ferney Voltaire, 2022
HAL
Dictionnaire des conventionnels, Centre international d'étude du XVIIIe siècle Ferney Voltaire, 2022
HAL
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::06e8b807cd58b9bb7ff6fa2e3336110e
https://hal-uco.archives-ouvertes.fr/hal-03689980
https://hal-uco.archives-ouvertes.fr/hal-03689980
Autor:
Sylvain Vergnet, Jean Phillipe Azulay, Isabelle Meunier, Audrey Riquet, Olivier Patat, Anna Castrioto, Laurent Pasquier, Cyril Charlin, Lena Damaj, Cécile Acquaviva, Nicolas Lebouc, Bérénice Doray, Cecilia Marelli, Morgane Pointaux, Pierre Meyer, Perrine Charles, Danielle Cuntz-Shadfar, Caroline Tillikete, Frederic Villega, Cathy Lieutard-Haag, Michel Koenig, François Rivier, Idriss Bousquet, Ganaëlle Remerand, Ulrike Walther-Louvier, Clarisse Carra-Dalliere, Victoria Gonzales, Alexandre Eusebio, Brigitte Chabrol, Emilie Carme, Pierre Labauge, Adrian Degardin, Elise Brischoux-Boucher, Brice Laurens, Laurent Kremer, Giovanni Castelnovo, Mélanie Fradin, Mehdi Benkirane, Karine Nguyen, Jean-Marie Ravel, Vincent Laugel, Emilien Bernard, Claire Guissart, Cyril Goizet, Samira Sissaoui, Agathe Roubertie, Christine Francannet, Sylvie Odent, Yosra Halleb, Xavier Ayrignac, Shahram Attarian, Fabienne Ory Magne, David Geneviève, Joel Victor Fluss, Alain Verloes, Anne Rolland, Martial Mallaret, Lydia Abou Haidar, Nadia Bahi-Buisson, David Baux, Catherine Sarret, Nicolas Carrière, Christine Coubes, Mathilde Renaud, Claire Ewenczyk, Patrick Calvas, Solène Frismand, Leila Lazaro, Bertrand Isidor, Annabelle Chaussenot, Sophie Julia, Valerie Fraix, Elsa Kaphan, Tatiana Witjas, Frédérique Fluchère, Mathieu Anheim, Christine Tranchant, William Camu, Eric Thouvenot, Lise Larrieu, Eric Bieth, Ariane Choumert, Raoul Morales, Marinha Costa Moreira, Elizabeth Ollagnon
Publikováno v:
Genetics in Medicine
Genetics in Medicine, Nature Publishing Group, In press, ⟨10.1038/s41436-021-01250-6⟩
Genetics in Medicine, Nature Publishing Group, 2021, ⟨10.1038/s41436-021-01250-6⟩
Genetics in Medicine, Nature Publishing Group, In press, ⟨10.1038/s41436-021-01250-6⟩
Genetics in Medicine, Nature Publishing Group, 2021, ⟨10.1038/s41436-021-01250-6⟩
International audience; Purpose: Diagnosis of inherited ataxia and related diseases represents a real challenge given the tremendous heterogeneity and clinical overlap of the various causes. We evaluated the efficacy of molecular diagnosis of these d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::babfbeb68f31ca6afb2b34ab5e5a2e4e
https://hal.archives-ouvertes.fr/hal-03282716
https://hal.archives-ouvertes.fr/hal-03282716
Autor:
Rima Nabbout, Patrick Berquin, Sylvie Odent, Mathieu Kuchenbuch, Gwenaël Le Guyader, Marieke F. van Dooren, Jamel Chelly, Edor Kabashi, Melanie Jennesson, Giulia Barcia, Cyril Mignot, Tayeb Sekhara, Alexandra Afenjar, Marlène Rio, Anne Rolland, Claude Besmond, Andrés Rodríguez-Sacristán Cascajo, Gaetano Terrone, Isabelle Marey, Boris Keren, Alice Goldenberg, A.S. Lebre, Heather C Mefford, Gaetan Lesca, Anne de Saint Martin, Susanna Negrin, Nathalie Dorison, Hélène Maurey, Agnès Guët, David Geneviève, Marie Claire Y. de Wit, Jeremy L. Freeman, Pierre Meyer, Thierry Billette de Villemeur, Ingrid E. Scheffer, Katherine B. Howell, Anca Nica, Raphael Levy, Martino Montomoli, Renzo Guerrini, Elena Parrini, Candace T. Myers, Bertrand Isidor, Alice Poisson, Marion Gérard, Salima El Chehadeh, Lynette G. Sadleir, Julien Durigneux, Pascal Vrielynck, Amy L Schneider, Emmanuel Scalais, Laurence Hubert, Sophie Dupont, Vesna Brankovic, Damien Lederer, Hervé Isnard, Delphine Breuillard, Claire Bar, Alberto Danieli, Diane Doummar, Arnold Munnich
Publikováno v:
Epilepsia
Epilepsia, 2020, 61 (11), pp.2461-2473. ⟨10.1111/epi.16679⟩
Epilepsia, Wiley, 2020, 61 (11), pp.2461-2473. ⟨10.1111/epi.16679⟩
Epilepsia, 61(11), 2461-2473. Wiley-Blackwell Publishing Ltd
Epilepsia, 2020, 61 (11), pp.2461-2473. ⟨10.1111/epi.16679⟩
Epilepsia, Wiley, 2020, 61 (11), pp.2461-2473. ⟨10.1111/epi.16679⟩
Epilepsia, 61(11), 2461-2473. Wiley-Blackwell Publishing Ltd
Objective: We aimed to delineate the phenotypic spectrum and long-term outcome of individuals with KCNB1 encephalopathy. Methods: We collected genetic, clinical, electroencephalographic, and imaging data of individuals with KCNB1 pathogenic variants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d3e62c02513d68aa9825d00009bfe7a
https://univ-rennes.hal.science/hal-02959318
https://univ-rennes.hal.science/hal-02959318