Результати пошуку - Lionel Carmant
- Показ 1 - 20 результатів із 20
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1
Seizures and Epilepsy: An Overview for Neuroscientists за авторством Carl E. Stafstrom, Lionel Carmant
Опубліковано 2015Revisão -
2
A retrospective study on aetiology based outcome of infantile spasms за авторством Georges Karvelas, Anne Lortie, Morris H. Scantlebury, Paul T. Duy, Patrick Cossette, Lionel Carmant
Опубліковано 2008Artigo -
3
Vagus nerve stimulation in pediatric epileptic syndromes за авторством Elsa Rossignol, Anne Lortie, Tammy Thomas, A. Bouthiller, Didier Scavarda, C Mercier, Lionel Carmant
Опубліковано 2008Artigo -
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The combination of subdural and depth electrodes for intracranial EEG investigation of suspected insular (perisylvian) epilepsy за авторством Werner Surbeck, Alain Bouthillier, Alexander G. Weil, Louis Crevier, Lionel Carmant, Anne Lortie, Philippe Major, Dang Khoa Nguyen
Опубліковано 2011Artigo -
6
Early-Life Stress Is Associated with Gender-Based Vulnerability to Epileptogenesis in Rat Pups за авторством Sébastien Desgent, Sandra Duss, Nathalie T. Sanon, Pablo Lema, Maxime Lévesque, David Hébert, Rose‐Marie Rébillard, Karine Bibeau, M. Brochu, Lionel Carmant
Опубліковано 2012Artigo -
7
Does vigabatrin treatment for infantile spasms cause visual field defects? An international multicentre study за авторством Raili Riikonen, Zvonka Rener‐Primec, Lionel Carmant, М. Ю. Дорофеева, Katalin Hollódy, Ilona Pálfiné Szabó, Branka S Krajnc, Gabriele Wohlrab, Iiris Sorri
Опубліковано 2014Artigo -
8
Non-invasive pre-surgical investigation of a 10 year-old epileptic boy using simultaneous EEG–NIRS за авторством Anne Gallagher, Maryse Lassonde, Danielle Bastien, Phetsamone Vannasing, Frédéric Lesage, Christophe Grova, Alain Bouthillier, Lionel Carmant, Franco Leporé, Renée Béland, Dang Khoa Nguyen
Опубліковано 2008Artigo -
9
Epilepsy surgery in the first 3 years of life: A Canadian survey за авторством 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
Опубліковано 2009Artigo -
10
KCC2 Regulates Dendritic Spine Formation in a Brain-Region Specific and BDNF Dependent Manner за авторством 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
Опубліковано 2018Artigo -
11
Current beliefs and attitudes regarding epilepsy in Mali за авторством 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
Опубліковано 2014Artigo -
12
The genetic landscape of infantile spasms за авторством 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
Опубліковано 2014Artigo -
13
Children's perspective of quality of life in epilepsy за авторством 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
Опубліковано 2015Artigo -
14
Decrease of SYNGAP1 in GABAergic cells impairs inhibitory synapse connectivity, synaptic inhibition and cognitive function за авторством 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
Опубліковано 2016Artigo -
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... за авторством 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
Опубліковано 2018Revisão -
16
<i>KCNQ2</i> encephalopathy за авторством 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
Опубліковано 2016Artigo -
17
Mutations in<i>SYNGAP1</i>in Autosomal Nonsyndromic Mental Retardation за авторством 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
Опубліковано 2009Artigo -
18
Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons за авторством 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
Опубліковано 2019Artigo -
19
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies за авторством 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
Опубліковано 2017Revisão -
20
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study за авторством 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
Опубліковано 2018Artigo
Інструменти для пошуку:
Пов'язані теми
Medicine
Epilepsy
Psychiatry
Biology
Pediatrics
Genetics
Internal medicine
Gene
Neuroscience
Psychology
Mutation
Anesthesia
Cohort
Phenotype
Surgery
Anticonvulsant
Candidate gene
Clinical psychology
Environmental health
Epilepsy surgery
Epilepsy syndromes
Etiology
Exome
Exome sequencing
Genome
Missense mutation
Pathology
Population
Receptor
Retrospective cohort study