Search Results - Nathalie Villeneuve

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  1. 1
    The ketogenic diet improves recently worsened focal epilepsy

    The ketogenic diet improves recently worsened focal epilepsy by Nathalie Villeneuve, Florence Pinton, Nadia Bahi‐Buisson, Olivier Dulac, Catherine Chiron, Rima Nabbout

    Published 2009
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  2. 2
    Glutamate Transporters Prevent the Generation of Seizures in the Developing Rat Neocortex

    Glutamate Transporters Prevent the Generation of Seizures in the Developing Rat Neocortex by Michaël Demarque, Nathalie Villeneuve, Jean‐Bernard Manent, Hélène Becq, Alfonso Represa, Yehezkel Ben‐Ari, Laurent Aniksztejn

    Published 2004
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  3. 3
    Atypical sulcal anatomy in young children with autism spectrum disorder

    Atypical sulcal anatomy in young children with autism spectrum disorder by Guillaume Auzias, Marine Viellard, Sylvain Takerkart, Nathalie Villeneuve, François Poinso, D. Da Fonséca, Nadine Girard, Christine Deruelle

    Published 2014
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  4. 4
    Unusual consequences of status epilepticus in Dravet syndrome

    Unusual consequences of status epilepticus in Dravet syndrome by Mathilde Chipaux, Nathalie Villeneuve, Pascal Sabouraud, Isabelle Desguerre, Nathalie Boddaert, Christel Depienne, Catherine Chiron, Olivier Dulac, Rima Nabbout

    Published 2010
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  5. 5
    Safety and efficacy of Gamma Knife radiosurgery in hypothalamic hamartomas with severe epilepsies: A prospective trial in 48 patients and review of the literature

    Safety and efficacy of Gamma Knife radiosurgery in hypothalamic hamartomas with severe epilepsies: A prospective trial in 48 patients and review of the literature by Jean Régis, M. Lagmari, Romain Carron, Motohiro Hayashi, Aileen McGonigal, Géraldine Daquin, Nathalie Villeneuve, Virginie Laguitton, Fabrice Bartoloméi, Patrick Chauvel

    Published 2017
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  6. 6
    Novel Compound Heterozygous Mutations in<i>TBC</i><i>1</i><i>D</i><i>24</i>Cause Familial Malignant Migrating Partial Seizures of Infancy

    Novel Compound Heterozygous Mutations in<i>TBC</i><i>1</i><i>D</i><i>24</i>Cause Familial Malignant Migrating Partial Seizures of Infancy by Mathieu Milh, Antonio Falace, Nathalie Villeneuve, Nicola Vanni, Pierre Cacciagli, Stefania Assereto, Rima Nabbout, Fabio Benfenati, Federico Zara, B. Chabrol, Laurent Villard, Anna Fassio

    Published 2013
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  7. 7
    Effects of bumetanide on neurobehavioral function in children and adolescents with autism spectrum disorders

    Effects of bumetanide on neurobehavioral function in children and adolescents with autism spectrum disorders by Éric Lemonnier, Nathalie Villeneuve, Sandrine Sonié, Sylvie Serret, Antoine Rosier, Jean‐Michel Roué, P. Brosset, Marine Viellard, Delphine Bernoux, S. Rondeau, Susanne Thümmler, Denis Ravel, Yehezkel Ben‐Ari

    Published 2017
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  8. 8
    Predictive Factors of Surgical Outcome in Frontal Lobe Epilepsy Explored with Stereoelectroencephalography

    Predictive Factors of Surgical Outcome in Frontal Lobe Epilepsy Explored with Stereoelectroencephalography by Francesca Bonini, Aileen McGonigal, Didier Scavarda, Romain Carron, Jean Régis, Henry Dufour, J.C. Peragut, Virginie Laguitton, Nathalie Villeneuve, Patrick Chauvel, Bernard Giusiano, Agnès Trébuchon, Fabrice Bartoloméi

    Published 2017
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  9. 9
    Recurrent mutations in the <i>CDKL5</i> gene: Genotype–phenotype relationships

    Recurrent mutations in the <i>CDKL5</i> gene: Genotype–phenotype relationships by Nadia Bahi‐Buisson, Nathalie Villeneuve, Emilie Caietta, Aurélia Jacquette, Hélène Maurey, Gert Matthijs, Hilde Van Esch, Andrée Delahaye‐Duriez, Anne Moncla, Mathieu Milh, Flore Zufferey, Bertrand Diebold, Thierry Bienvenu

    Published 2012
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  10. 10
    Seizure‐onset patterns in focal cortical dysplasia and neurodevelopmental tumors: Relationship with surgical prognosis and neuropathologic subtypes

    Seizure‐onset patterns in focal cortical dysplasia and neurodevelopmental tumors: Relationship with surgical prognosis and neuropathologic subtypes by Stanislas Lagarde, Francesca Bonini, Aileen McGonigal, Patrick Chauvel, Martine Gavaret, Didier Scavarda, Romain Carron, Jean Régis, Sandrine Aubert, Nathalie Villeneuve, Bernard Giusiano, Dominique Figarella‐Branger, Agnès Trébuchon, Fabrice Bartolomei

    Published 2016
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  11. 11
    Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations

    Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations by Mathieu Milh, Nathalie Villeneuve, Mondher Chouchane, Anna Kaminśka, Cécile Laroche, Marie Anne Barthez, Cyril Gitiaux, Céline Bartoli, Ana Borges-Correia, Pierre Cacciagli, Cécile Mignon‐Ravix, Hélène Cuberos, B. Chabrol, Laurent Villard

    Published 2011
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  12. 12
    Stereoelectroencephalographic exploration and surgical outcome in Lennox–Gastaut syndrome

    Stereoelectroencephalographic exploration and surgical outcome in Lennox–Gastaut syndrome by Soomi Cho, Julia Makhalova, Samuel Medina Villalon, Nathalie Villeneuve, Agnès Trébuchon, Manel Krouma, Didier Scavarda, Anne Lépine, Mathieu Milh, Romain Carron, Francesca Bonini, Géraldine Daquin, Sandrine Aubert, Stanislas Lagarde, Francesca Pizzo, Fabrice Bartoloméi

    Published 2025
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  13. 13
    Fenfluramine for Treatment-Resistant Seizures in Patients With Dravet Syndrome Receiving Stiripentol-Inclusive Regimens

    Fenfluramine for Treatment-Resistant Seizures in Patients With Dravet Syndrome Receiving Stiripentol-Inclusive Regimens by Rima Nabbout, Arun Mistry, Sameer M. Zuberi, Nathalie Villeneuve, António Gil‐Nagel, Rocío Sánchez‐Carpintero, Ulrich Stephani, Linda Laux, Elaine Wirrell, Kelly G. Knupp, Catherine Chiron, Gail Farfel, Bradley S. Galer, Glenn Morrison, Michael Lock, Anupam Agarwal, Stéphane Auvin

    Published 2019
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  14. 14
    Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome

    Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome by Christel Depienne, Oriane Trouillard, Isabelle Gourfinkel‐An, Cécile Saint‐Martin, Delphine Bouteiller, Denis Graber, Marie‐Anne Barthez‐Carpentier, Agnès Gautier, Nathalie Villeneuve, Charlotte Dravet, Marie-Odile Livet, Clotilde Rivier-Ringenbach, Claude Adam, Sabrina Dupont, Stéphanie Baulac, Delphine Héron, Rima Nabbout, Eric Leguern

    Published 2010
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  15. 15
    Anti–tumor necrosis factor alpha therapy (adalimumab) in Rasmussen's encephalitis: An open pilot study

    Anti–tumor necrosis factor alpha therapy (adalimumab) in Rasmussen's encephalitis: An open pilot study by Stanislas Lagarde, Nathalie Villeneuve, Agnès Trébuchon, Elsa Kaphan, Anne Lépine, Aileen McGonigal, Agathe Roubertie, Marie‐Anne J. Barthez, Valérie Trommsdorff, Jérémie Lefranc, Samer Wehbi, Vincent des Portes, Virginie Laguitton, Pierre Quartier, Didier Scavarda, Bernard Giusiano, Mathieu Milh, Christine Bulteau, Fabrice Bartoloméi

    Published 2016
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  16. 16
    Epilepsy with migrating focal seizures

    Epilepsy with migrating focal seizures by Giulia Barcia, Nicole Chémaly, Mathieu Kuchenbuch, Monika Eisermann, Stéphanie Gobin‐Limballe, Viorica Ciorna, Alfons Macaya, Laëtitia Lambert, Fanny Dubois, Diane Doummar, Thierry Billette de Villemeur, Nathalie Villeneuve, Marie-Anne Barthez, Caroline Nava, Nathalie Boddaert, Anna Kaminśka, Nadia Bahi‐Buisson, Mathieu Milh, Stéphane Auvin, Jean‐Paul Bonnefont, Rima Nabbout

    Published 2019
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  17. 17
    A broad spectrum of clinical presentations in congenital disorders of glycosylation I: a series of 26 cases

    A broad spectrum of clinical presentations in congenital disorders of glycosylation I: a series of 26 cases by Pascale de Lonlay, Nathalie Seta, Sandrine Vuillaumier Barrot, B. Chabrol, Valérie Drouin, Bernard Gabriel, Hubert Journel, M. Kretz, J. Laurent, M. Le Merrer, A. Leroy, D. Pedespan, P. Sardá, Nathalie Villeneuve, J. Schmitz, Emile Van Schaftingen, Gert Matthijs, Jaak Jaeken, Christian Körner, A. Munnich, J. M. Saudubray, Valérie Cormier‐Daire

    Published 2001
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  18. 18
    A common pattern of brain MRI imaging in mitochondrial diseases with complex I deficiency

    A common pattern of brain MRI imaging in mitochondrial diseases with complex I deficiency by Anne-Sophie Lèbre, Marlène Rio, L. Faivre d'Arcier, Déwy Vernerey, P. Landrieu, Abdelhamid Slama, Claude Jardel, P. Laforet, Diana Rodriguez, Nathalie Dorison, Damien Galanaud, B. Chabrol, Véronique Paquis‐Flucklinger, D. Grévent, Simon Edvardson, Julie Steffann, Benoît Funalot, Nathalie Villeneuve, Vassili Valayannopoulos, Pascale de Lonlay, I. Desguerre, Françis Brunelle, Jean‐Paul Bonnefont, Agnès Rötig, Arnold Münnich, Nathalie Boddaert

    Published 2010
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  19. 19
    CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patients

    CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patients by Marie Le Roux, Magalie Barth, Sophie Guéden, Patrick Desbordes de Cepoy, Alec Aeby, Catheline Vilain, Édouard Hirsch, Anne de Saint Martin, Vincent des Portes, Gaëtan Lesca, Audrey Riquet, Laurence Chaton, Nathalie Villeneuve, Laurent Villard, Claude Cancès, Luc Valton, Florence Renaldo, Anne‐Isabelle Vermersch, Cécilia Altuzarra, Marie-Ange Nguyen-Morel, Julien Van‐Gils, Chloé Angelini, Arnaud Biraben, Lionel Arnaud, Florence Riant, Patrick Van Bogaert

    Published 2021
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  20. 20
    Epileptic patients with de novo <i><scp>STXBP</scp>1</i> mutations: Key clinical features based on 24 cases

    Epileptic patients with de novo <i><scp>STXBP</scp>1</i> mutations: Key clinical features based on 24 cases by Chloé Di Meglio, Gaëtan Lesca, Nathalie Villeneuve, Caroline Lacoste, Affef Abidi, Pierre Cacciagli, Cécilia Altuzarra, Agathe Roubertie, Alexandra Afenjar, Florence Renaldo‐Robin, Bertrand Isidor, Agnès Gautier, Marie Husson, Claude Cancès, Julia Métreau, Cécile Laroche, Mondher Chouchane, Dorothée Ville, Stéphanie Marignier, Christelle Rougeot, Marine Lebrun, Anne de Saint Martin, Alexandra Perez, Audrey Riquet, Catherine Badens, Chantal Missirian, Nicole Philip, B. Chabrol, Laurent Villard, Mathieu Milh

    Published 2015
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