検索結果 - Lionel Carmant

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  1. 1
    Seizures and Epilepsy: An Overview for Neuroscientists

    Seizures and Epilepsy: An Overview for Neuroscientists 著者: Carl E. Stafstrom, Lionel Carmant

    出版事項 2015
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  2. 2
    A retrospective study on aetiology based outcome of infantile spasms

    A retrospective study on aetiology based outcome of infantile spasms 著者: Georges Karvelas, Anne Lortie, Morris H. Scantlebury, Paul T. Duy, Patrick Cossette, Lionel Carmant

    出版事項 2008
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  3. 3
    Vagus nerve stimulation in pediatric epileptic syndromes

    Vagus nerve stimulation in pediatric epileptic syndromes 著者: Elsa Rossignol, Anne Lortie, Tammy Thomas, A. Bouthiller, Didier Scavarda, C Mercier, Lionel Carmant

    出版事項 2008
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  4. 4
    Language development in children with congenital heart disease aged 12–24 months

    Language development in children with congenital heart disease aged 12–24 months 著者: Solène Fourdain, Ariane St-Denis, Julien Harvey, Ala Birca, Lionel Carmant, Anne Gallagher, Natacha Trudeau

    出版事項 2019
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  5. 5
    The combination of subdural and depth electrodes for intracranial EEG investigation of suspected insular (perisylvian) epilepsy

    The combination of subdural and depth electrodes for intracranial EEG investigation of suspected insular (perisylvian) epilepsy 著者: Werner Surbeck, Alain Bouthillier, Alexander G. Weil, Louis Crevier, Lionel Carmant, Anne Lortie, Philippe Major, Dang Khoa Nguyen

    出版事項 2011
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  6. 6
    Early-Life Stress Is Associated with Gender-Based Vulnerability to Epileptogenesis in Rat Pups

    Early-Life Stress Is Associated with Gender-Based Vulnerability to Epileptogenesis in Rat Pups 著者: Sébastien Desgent, Sandra Duss, Nathalie T. Sanon, Pablo Lema, Maxime Lévesque, David Hébert, Rose‐Marie Rébillard, Karine Bibeau, M. Brochu, Lionel Carmant

    出版事項 2012
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  7. 7
    Does vigabatrin treatment for infantile spasms cause visual field defects? An international multicentre study

    Does vigabatrin treatment for infantile spasms cause visual field defects? An international multicentre study 著者: Raili Riikonen, Zvonka Rener‐Primec, Lionel Carmant, М. Ю. Дорофеева, Katalin Hollódy, Ilona Pálfiné Szabó, Branka S Krajnc, Gabriele Wohlrab, Iiris Sorri

    出版事項 2014
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  8. 8
    Non-invasive pre-surgical investigation of a 10 year-old epileptic boy using simultaneous EEG–NIRS

    Non-invasive pre-surgical investigation of a 10 year-old epileptic boy using simultaneous EEG–NIRS 著者: Anne Gallagher, Maryse Lassonde, Danielle Bastien, Phetsamone Vannasing, Frédéric Lesage, Christophe Grova, Alain Bouthillier, Lionel Carmant, Franco Leporé, Renée Béland, Dang Khoa Nguyen

    出版事項 2008
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  9. 9
    Epilepsy surgery in the first 3 years of life: A Canadian survey

    Epilepsy surgery in the first 3 years of life: A Canadian survey 著者: Paul Steinbok, Peter Gan, Mary Connolly, Lionel Carmant, D. Barry Sinclair, James T. Rutka, Robert Griebel, Keith Aronyk, Walter Hader, Enrique C. G. Ventureyra, Jeffrey Atkinson

    出版事項 2009
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  10. 10
    KCC2 Regulates Dendritic Spine Formation in a Brain-Region Specific and BDNF Dependent Manner

    KCC2 Regulates Dendritic Spine Formation in a Brain-Region Specific and BDNF Dependent Manner 著者: Patricia N. Awad, Clara A. Amegandjin, Joanna Szczurkowska, Josianne Nuñes Carriço, Antônia Sâmia Fernandes do Nascimento, Elie Baho, Bidisha Chattopadhyaya, Laura Cancedda, Lionel Carmant, Graziella Di Cristo

    出版事項 2018
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  11. 11
    Current beliefs and attitudes regarding epilepsy in Mali

    Current beliefs and attitudes regarding epilepsy in Mali 著者: Youssoufa Maiga, Mohamed Albakaye, Lanssana Laho Diallo, Broulaye Traoré, Yacouba Cissoko, Hassane Seybou, Sara Diakite, K. Clare McCaughey, Najib Kissani, Valeria Diaconu, Danielle Buch, Kassim Kayentoa, Lionel Carmant

    出版事項 2014
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  12. 12
    The genetic landscape of infantile spasms

    The genetic landscape of infantile spasms 著者: Jacques L. Michaud, Mathieu Lachance, Fadi F. Hamdan, Lionel Carmant, Anne Lortie, Paola Diadori, Philippe Major, Inge A. Meijer, Emmanuelle Lemyre, Patrick Cossette, Heather C. Mefford, Guy A. Rouleau, Elsa Rossignol

    出版事項 2014
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  13. 13
    Children's perspective of quality of life in epilepsy

    Children's perspective of quality of life in epilepsy 著者: Nora Fayed, Aileen M. Davis, David L. Streiner, Peter Rosenbaum, Charles E. Cunningham, Lucyna Lach, Michael H. Boyle, Gabriel M. Ronen, Mary Connolly, Luis Bello‐Espinosa, Mubeen F. Rafay, Juan Pablo Appendino, Michael Shevell, Lionel Carmant

    出版事項 2015
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  14. 14
    Decrease of SYNGAP1 in GABAergic cells impairs inhibitory synapse connectivity, synaptic inhibition and cognitive function

    Decrease of SYNGAP1 in GABAergic cells impairs inhibitory synapse connectivity, synaptic inhibition and cognitive function 著者: Martin H. Berryer, Bidisha Chattopadhyaya, Paul Xing, Ilse Riebe, Ciprian M. Bosoi, Nathalie T. Sanon, Judith Antoine‐Bertrand, Maxime Lévesque, Massimo Avoli, Fadi F. Hamdan, Lionel Carmant, Nathalie Lamarche‐Vane, Jean‐Claude Lacaille, Jacques L. Michaud, Graziella Di Cristo

    出版事項 2016
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  15. 15
    Systematic review of the screening, diagnosis, and management of <scp>ADHD</scp> in children with epilepsy. Consensus paper of the Task Force on Comorbidities of the <scp>ILAE</scp> Pediatric Commission

    Systematic review of the screening, diagnosis, and management of <scp>ADHD</scp> in children with epilepsy. Consensus paper of the Task Force on Comorbidities of the <scp>ILAE</scp... 著者: Stéphane Auvin, Elaine Wirrell, Kirsten A. Donald, Madison M. Berl, Hans Hartmann, Kette D. Valente, Patrick Van Bogaert, J. Helen Cross, Makiko Ōsawa, Hideaki Kanemura, Masao Aihara, Marilisa M. Guerreiro, Pauline Samia, Kollencheri Puthenveettil Vinayan, Mary Lou Smith, Lionel Carmant, Michael Kerr, Bruce P. Hermann, David Dunn, Jo M. Wilmshurst

    出版事項 2018
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  16. 16
    <i>KCNQ2</i> encephalopathy

    <i>KCNQ2</i> encephalopathy 著者: J Gordon Millichap, Kristen Park, Tammy N. Tsuchida, Bruria Ben‐Zeev, Lionel Carmant, Robert Flamini, Nishtha Joshi, Paul M. Levisohn, Eric D. Marsh, Srishti Nangia, Vinodh Narayanan, Xilma R. Ortiz‐González, Marc C. Patterson, Phillip L. Pearl, Brenda E. Porter, Keri Ramsey, Emily McGinnis, Maurizio Taglialatela, Molly Tracy, Baouyen Tran, Charu Venkatesan, Sarah Weckhuysen, Edward C. Cooper

    出版事項 2016
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  17. 17
    Mutations in<i>SYNGAP1</i>in Autosomal Nonsyndromic Mental Retardation

    Mutations in<i>SYNGAP1</i>in Autosomal Nonsyndromic Mental Retardation 著者: Fadi F. Hamdan, Julie Gauthier, Dan Spiegelman, Anne Noreau, Yanlian Yang, Stéphanie Pellerin, Sylvia Dobrzeniecka, Mélanie Côté, Elizabeth Perreau-Linck, Lionel Carmant, Guy D’Anjou, Éric Fombonne, Anjené Addington, Judith L. Rapoport, Lynn E. DeLisi, Marie‐Odile Krebs, Fayçal Mouaffak, Ridha Joober, Laurent Mottron, Pierre Drapeau, Claude Marineau, Ronald G. Lafrenière, Jean Claude Lacaille, Guy A. Rouleau, Jacques L. Michaud

    出版事項 2009
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  18. 18
    Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons

    Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons 著者: Scott C. Bell, Justine Rousseau, Huashan Peng, Zahia Aouabed, Pierre Priam, Jean-Francois Theroux, Malvin Jefri, Arnaud Tanti, Hanrong Wu, Ilaria Kolobova, Heika Silviera, Karla Manzano-Vargas, Sophie Ehresmann, Fadi F. Hamdan, Nuwan C. Hettige, Xin Zhang, Lilit Antonyan, Christina Nassif, Lina Ghaloul‐Gonzalez, Jessica Sebastian, Jerry Vockley, Amber G. Begtrup, Ingrid M. Wentzensen, Amy Crunk, Robert D. Nicholls, Kristin Herman, Joshua L. Deignan, Walla Al‐Hertani, Stéphanie Efthymiou, Vincenzo Salpietro, Noriko Miyake, Yoshio Makita, Naomichi Matsumoto, Rune Østern, Gunnar Houge, Maria Hafström, Emily Fassi, Henry Houlden, Jolien S. Klein Wassink‐Ruiter, Dominic Nelson, Amy Goldstein, Tabib Dabir, Julien Van‐Gils, Thomas Bourgeron, Richard Delorme, Gregory M. Cooper, José E. Martínez, Candice R. Finnila, Lionel Carmant, Anne Lortie, Renske Oegema, Koen L.I. van Gassen, Sarju Mehta, Dagmar Huhle, Rami Abou Jamra, Sonja Martin, Han G. Brunner, Dick Lindhout, Margaret Au, John M. Graham, Christine Coubes, Gustavo Turecki, Simon Gravel, Naguib Mechawar, Elsa Rossignol, Jacques L. Michaud, Julie Lessard, Carl Ernst, Philippe M. Campeau

    出版事項 2019
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  19. 19
    High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies

    High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies 著者: Fadi F. Hamdan, Candace T. Myers, Patrick Cossette, Philippe Lemay, Dan Spiegelman, Alexandre D. Laporte, Christina Nassif, Ousmane Diallo, Jean Monlong, Maxime Cadieux‐Dion, Sylvia Dobrzeniecka, Caroline Meloche, Kyle Retterer, Megan T. Cho, Jill A. Rosenfeld, Weimin Bi, Christine Massicotte, Marguerite Miguet, Ledia Brunga, Brigid M. Regan, Kelly Mo, Cory Tam, Amy L. Schneider, Georgie Hollingsworth, David Fitzpatrick, Alan Donaldson, Natalie Canham, Edward Blair, Bronwyn Kerr, Andrew E. Fry, Rhys H. Thomas, Joss Shelagh, Jane A. Hurst, Helen Brittain, Moira Blyth, Robert Roger Lebel, Erica H. Gerkes, Laura Davis‐Keppen, Quinn Stein, Wendy K. Chung, Sara J. Dorison, Paul J. Benke, Emily Fassi, Nicole Corsten‐Janssen, Erik‐Jan Kamsteeg, Frédéric Tran Mau‐Them, Ange‐Line Bruel, Alain Verloès, Katrin Õunap, Monica H. Wojcik, Dara V.F. Albert, Sunita Venkateswaran, Tyson L. Ware, Dean Jones, Y. C. Liu, Shekeeb S. Mohammad, Peyman Bizargity, Carlos A. Bacino, Vincenzo Leuzzi, Simone Martinelli, Bruno Dallapiccola, Marco Tartaglia, Lubov Blumkin, Klaas J. Wierenga, Gabriela Purcarin, James J. O’Byrne, Sylvia Stöckler, Anna Lehman, Boris Keren, Marie‐Christine Nouguès, Cyril Mignot, Stéphane Auvin, Caroline Nava, Susan M. Hiatt, Martina Bebin, Yunru Shao, Fernando Scaglia, Seema R. Lalani, Richard E. Frye, Imad T. Jarjour, Stéphanie Jacques, Renee-Myriam Boucher, Émilie Riou, Myriam Srour, Lionel Carmant, Anne Lortie, Philippe Major, Paola Diadori, François Dubeau, Guy D’Anjou, Guillaume Bourque, Samuel F. Berkovic, Lynette G. Sadleir, Philippe M. Campeau, Zoha Kibar, Ronald G. Lafrenière, Simon Girard, Saadet Mercimek‐Mahmutoglu, Cyrus Boelman, Guy A. Rouleau

    出版事項 2017
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  20. 20
    Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

    Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study 著者: Patrick May, Simon Girard, Merle Harrer, Dheeraj Reddy Bobbili, Julian Schubert, Stefan Wolking, Felicitas Becker, Pamela Lachance‐Touchette, Caroline Meloche, Micheline Gravel, Cristina Elena Niturad, Julia Knaus, Carolien G. F. de Kovel, Mohamad Toliat, Anne Polvi, Michele Iacomino, Rosa Guerrero, Stéphanie Baulac, Carla Marini, Holger Thiele, Janine Altmüller, Kamel Jabbari, Ann‐Kathrin Ruppert, Wiktor Jurkowski, Dennis Lal, Raffaella Rusconi, Sandrine Cestèle, Benedetta Terragni, Ian D. Coombs, Christopher A. Reid, Pasquale Striano, Hande Çağlayan, Auli Sirén, Kate V. Everett, Rikke S. Møller, Helle Hjalgrim, Hiltrud Muhle, Ingo Helbig, Wolfram S. Kunz, Yvonne G. Weber, Sarah Weckhuysen, Peter De Jonghe, Sanjay M. Sisodiya, Rima Nabbout, Silvana Franceschetti, Antonietta Coppola, Maria Stella Vari, Dorothee Kasteleijn‐Nolst Trenité, Betül Baykan, Uğur Özbek, Nerses Bebek, Karl Martin Klein, Felix Rosenow, Dang Khoa Nguyen, François Dubeau, Lionel Carmant, Anne Lortie, Richard Desbiens, Jean-François Clément, Cécile Cieuta‐Walti, Graeme J. Sills, Pauls Auce, Ben Francis, Michael R. Johnson, Anthony G Marson, Bianca Berghuis, Josemir W. Sander, Andreja Avberšek, Mark McCormack, Gianpiero L. Cavalleri, Norman Delanty, Chantal Depondt, Martin Krenn, Fritz Zimprich, Sarah Peter, Marina Nikanorova, Robert Kraaij, Jeroen van Rooij, Rudi Balling, M. Arfan Ikram, André G. Uitterlinden, G. Avanzini, Stéphanie Schorge, Steven Petrou, Massimo Mantegazza, Thomas Sander, Eric LeGuern, José M. Serratosa, Bobby P.C. Koeleman, Aarno Palotie, Anna‐Elina Lehesjoki, Michael Nothnagel, Peter Nürnberg, Snezana Maljevic, Federico Zara, Patrick Cossette, Roland Krause, Holger Lerche, Patrick May, Simon Girard

    出版事項 2018
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