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Fabienne Picard

Showing results (61-70 of 77) with videos related to

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Swiss Medical Weekly|December 31, 2020
Early experimental COVID-19 therapies: associations with length of hospital stay, mortality and related costsNathalie Vernaz, Thomas Agoritsas, Alexandra Calmy, et al.
Epilepsy Research|August 8, 2007
Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsyElodie Chabrol, Isabelle Gourfinkel-An, Ingrid E Scheffer, et al.
Annals of Neurology|January 28, 2015
Familial focal epilepsy with focal cortical dysplasia due to DEPDC5 mutationsStéphanie Baulac, Saeko Ishida, Elise Marsan, et al.
Neurology. Genetics|April 12, 2016
Novel GABRG2 mutations cause familial febrile seizuresMorgane Boillot, Mélanie Morin-Brureau, Fabienne Picard, et al.
Epilepsia|May 14, 2016
Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasiaSarah Weckhuysen, Elise Marsan, Virginie Lambrecq, et al.
Neurology|June 30, 2012
PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European populationAurélie Méneret, David Grabli, Christel Depienne, et al.
Archives of Neurology|May 11, 2011
SCA15 due to large ITPR1 deletions in a cohort of 333 white families with dominant ataxiaCecilia Marelli, Joyce van de Leemput, Janel O Johnson, et al.
Brain : a Journal of Neurology|June 4, 2009
Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystoniaFabienne Clot, David Grabli, Cécile Cazeneuve, et al.
Neurology|May 13, 2014
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsyFabienne Picard, Periklis Makrythanasis, Vincent Navarro, et al.
Epilepsy & Behavior : E&B|August 16, 2015
Third International Congress on Epilepsy, Brain and Mind: Part 1Amos D Korczyn, Steven C Schachter, Jana Amlerova, et al.
Pageof 8

Showing results (61-70 of 77) with videos related to

Sort By:
Pageof 8
Swiss Medical Weekly|December 31, 2020
Early experimental COVID-19 therapies: associations with length of hospital stay, mortality and related costsNathalie Vernaz, Thomas Agoritsas, Alexandra Calmy, et al.
Epilepsy Research|August 8, 2007
Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsyElodie Chabrol, Isabelle Gourfinkel-An, Ingrid E Scheffer, et al.
Annals of Neurology|January 28, 2015
Familial focal epilepsy with focal cortical dysplasia due to DEPDC5 mutationsStéphanie Baulac, Saeko Ishida, Elise Marsan, et al.
Neurology. Genetics|April 12, 2016
Novel GABRG2 mutations cause familial febrile seizuresMorgane Boillot, Mélanie Morin-Brureau, Fabienne Picard, et al.
Epilepsia|May 14, 2016
Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasiaSarah Weckhuysen, Elise Marsan, Virginie Lambrecq, et al.
Neurology|June 30, 2012
PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European populationAurélie Méneret, David Grabli, Christel Depienne, et al.
Archives of Neurology|May 11, 2011
SCA15 due to large ITPR1 deletions in a cohort of 333 white families with dominant ataxiaCecilia Marelli, Joyce van de Leemput, Janel O Johnson, et al.
Brain : a Journal of Neurology|June 4, 2009
Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystoniaFabienne Clot, David Grabli, Cécile Cazeneuve, et al.
Neurology|May 13, 2014
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsyFabienne Picard, Periklis Makrythanasis, Vincent Navarro, et al.
Epilepsy & Behavior : E&B|August 16, 2015
Third International Congress on Epilepsy, Brain and Mind: Part 1Amos D Korczyn, Steven C Schachter, Jana Amlerova, et al.
Pageof 8