Zobrazeno 1 - 10
of 122
pro vyhledávání: '"Barthez, Marie Anne"'
Autor:
Viollet, Louis M., Swoboda, Kathryn J., Mao, Rong, Best, Hunter, Ha, Youna, Toutain, Annick, Guyant-Marechal, Lucie, Laroche-Raynaud, Cecile, Ghorab, Karima, Barthez, Marie Anne, Pedespan, Jean Michel, Hernandorena, Xavier, Lia, Anne-Sophie, Deleuze, Jean-Francois, Masson, Cecile, Nelson, Isabelle, Nectoux, Juliette, Si, Yue
Publikováno v:
In European Journal of Medical Genetics December 2020 63(12)
Publikováno v:
In Lingua February 2011 121(3):423-441
Autor:
Hommet, Caroline, Vidal, Julie, Roux, Sylvie, Blanc, Romuald, Barthez, Marie Anne, De Becque, Brigitte, Barthelemy, Catherine, Bruneau, Nicole, Gomot, Marie
Publikováno v:
In Neuropsychologia 2009 47(3):761-770
Autor:
Panagiotakaki, Eleni, Doummar, Diane, Nogue, Erika, Nagot, Nicolas, Lesca, Gaetan, Riant, Florence, Nicole, Sophie, Delaygue, Charlene, Barthez, Marie Anne, Nassogne, Marie Cécile, Dusser, Anne, Vallée, Louis, Billette, Thierry, Bourgeois, Marie, Ioos, Christine, Gitiaux, Cyril, Laroche, Cécile, Milh, Mathieu, Portes, Vincent Des, Arzimanoglou, Alexis, Roubertie, Agathe, AHC–Movement Disorder Study Group
Publikováno v:
Neurology
Neurology, American Academy of Neurology, 2020, 94 (13), pp.e1378-e1385. ⟨10.1212/WNL.0000000000009175⟩
Neurology, Vol. 94, no.13, p. e1378-e1385 (2020)
Neurology, 2020, 94 (13), pp.e1378-e1385. ⟨10.1212/WNL.0000000000009175⟩
Neurology, American Academy of Neurology, 2020, 94 (13), pp.e1378-e1385. ⟨10.1212/WNL.0000000000009175⟩
Neurology, Vol. 94, no.13, p. e1378-e1385 (2020)
Neurology, 2020, 94 (13), pp.e1378-e1385. ⟨10.1212/WNL.0000000000009175⟩
ObjectiveTo assess nonparoxysmal movement disorders inATP1A3mutation-positive patients with alternating hemiplegia of childhood (AHC).MethodsTwenty-eight patients underwent neurologic examination with particular focus on movement phenomenology by a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43e69df76f0c09dc0d693bc3e7577592
https://hal.archives-ouvertes.fr/hal-02533319
https://hal.archives-ouvertes.fr/hal-02533319
Akademický článek
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Publikováno v:
In Brain and Language 2005 92(3):300-308
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
Barcia, Giulia, Chemaly, Nicole, Kuchenbuch, Mathieu, Eisermann, Monika, Gobin-Limballe, Stéphanie, Ciorna, Viorica, Macaya Ruiz, Alfons, Lambert, Laetitia, Dubois, Fanny, Doummar, Diane, Billette de Villemeur, Thierry, Villeneuve, Nathalie, Barthez, Marie-Anne, Nava, Caroline, Boddaert, Nathalie, Kaminska, Anna, Bahi-Buisson, Nadia, Milh, Mathieu, Auvin, Stéphane, Bonnefont, Jean-Paul, Nabbout, Rima, Universitat Autònoma de Barcelona. Departament de Pediatria, Obstetrícia i Ginecologia i de Medicina Preventiva i Salut Pública
Publikováno v:
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Recercat. Dipósit de la Recerca de Catalunya
instname
Universitat Autònoma de Barcelona
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Recercat. Dipósit de la Recerca de Catalunya
instname
To report new sporadic cases and 1 family with epilepsy of infancy with migrating focal seizures (EIMFSs) due to KCNT1 gain-of-function and to assess therapies' efficacy including quinidine. We reviewed the clinical, EEG, and molecular data of 17 new
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2f544e1ba6b97070a0121ee4be68e4f2
https://ddd.uab.cat/record/227891
https://ddd.uab.cat/record/227891
Autor:
Barcia, Giulia, Chemaly, Nicole, Kuchenbuch, Mathieu, Eisermann, Monika, Gobin-Limballe, Stephanie, Ciorna, Viorica, Macaya, Alfons, Lambert, Laetitia, Dubois, Fanny, Doummar, Diane, Billette, Thierry, Villeneuve, Nathalie, Barthez, Marie-Anne, Nava, Caroline, Boddaert, Nathalie, Kaminska, Anna, Bahi-Buisson, Nadia, Milh, Mathieu, Auvin, Stephane, Bonnefont, Jean-Paul, Nabbout, Rima
Publikováno v:
Neurology: Genetics
Neurology Genetics
Neurology Genetics, American Academy of Neurology, 2019, 5 (6), pp.e363. ⟨10.1212/NXG.0000000000000363⟩
Neurology Genetics, 2019, 5 (6), pp.e363. ⟨10.1212/NXG.0000000000000363⟩
Neurology Genetics
Neurology Genetics, American Academy of Neurology, 2019, 5 (6), pp.e363. ⟨10.1212/NXG.0000000000000363⟩
Neurology Genetics, 2019, 5 (6), pp.e363. ⟨10.1212/NXG.0000000000000363⟩
International audience; Objective To report new sporadic cases and 1 family with epilepsy of infancy with migrating focal seizures (EIMFSs) due to KCNT1 gain-of-function and to assess therapies' efficacy including quinidine.Methods We reviewed the cl
Autor:
Ng Wing Tin Sophie, Martin-Duverneuil Nadine, Idbaih Ahmed, Garel Catherine, Ribeiro Maria, Parker Judith, Defachelles Anne-Sophie, Lambilliotte Anne, Barkaoui Mohamed, Munzer Martine, Gardembas Martine, Sibilia Jean, Lutz Patrick, Fior Renato, Polak Michel, Robert Alain, Aumaitre Olivier, Plantaz Dominique, Armari-Alla Corinne, Genereau Thierry, Berard Perrine, Talom Ghislain, Pennaforte Jean-Loup, Le Pointe Hubert, Barthez Marie-Anne, Couillault Gérard, Haroche Julien, Mokhtari Karima, Donadieu Jean, Hoang-Xuan Khê
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 6, Iss 1, p 83 (2011)
Abstract Background Vinblastine (VBL) is the standard treatment for systemic Langerhans cell histiocytosis (LCH), but little is known about its efficacy in central nervous system (CNS) mass lesions. Methods A retrospective chart review was conducted.
Externí odkaz:
https://doaj.org/article/cefabb8b72f64259998acf58baf0ad2c