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Swiss Medical Weekly
|
December 31, 2020
Early experimental COVID-19 therapies: associations with length of hospital stay, mortality and related costs
Nathalie 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 epilepsy
Elodie 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 mutations
Stéphanie Baulac, Saeko Ishida, Elise Marsan, et al.
Neurology. Genetics
|
April 12, 2016
Novel GABRG2 mutations cause familial febrile seizures
Morgane Boillot, Mélanie Morin-Brureau, Fabienne Picard, et al.
Epilepsia
|
May 14, 2016
Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia
Sarah Weckhuysen, Elise Marsan, Virginie Lambrecq, et al.
Neurology
|
June 30, 2012
PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European population
Aurélie 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 ataxia
Cecilia 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 dystonia
Fabienne Clot, David Grabli, Cécile Cazeneuve, et al.
Neurology
|
May 13, 2014
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy
Fabienne Picard, Periklis Makrythanasis, Vincent Navarro, et al.
Epilepsy & Behavior : E&B
|
August 16, 2015
Third International Congress on Epilepsy, Brain and Mind: Part 1
Amos D Korczyn, Steven C Schachter, Jana Amlerova, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 77) with videos related to
Sort By:
Page
of 8
Swiss Medical Weekly
|
December 31, 2020
Early experimental COVID-19 therapies: associations with length of hospital stay, mortality and related costs
Nathalie 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 epilepsy
Elodie 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 mutations
Stéphanie Baulac, Saeko Ishida, Elise Marsan, et al.
Neurology. Genetics
|
April 12, 2016
Novel GABRG2 mutations cause familial febrile seizures
Morgane Boillot, Mélanie Morin-Brureau, Fabienne Picard, et al.
Epilepsia
|
May 14, 2016
Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia
Sarah Weckhuysen, Elise Marsan, Virginie Lambrecq, et al.
Neurology
|
June 30, 2012
PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European population
Aurélie 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 ataxia
Cecilia 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 dystonia
Fabienne Clot, David Grabli, Cécile Cazeneuve, et al.
Neurology
|
May 13, 2014
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy
Fabienne Picard, Periklis Makrythanasis, Vincent Navarro, et al.
Epilepsy & Behavior : E&B
|
August 16, 2015
Third International Congress on Epilepsy, Brain and Mind: Part 1
Amos D Korczyn, Steven C Schachter, Jana Amlerova, et al.
Page
of 8