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Thomas Sander

Showing results (91-100 of 136) with videos related to

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European Archives of Psychiatry and Clinical Neuroscience|April 7, 2005
Polymorphisms in the NMDA subunit 2B are not associated with alcohol dependence and alcohol withdrawal-induced seizures and delirium tremensAndre Tadic, Norbert Dahmen, Armin Szegedi, et al.
Annals of Neurology|June 2, 2005
Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsyUlrike Tauer, Susanne Lorenz, Kirsten P Lenzen, et al.
Journal of Neurology|April 9, 2013
EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvementRoberta Biancheri, Denise Cassandrini, Francesca Pinto, et al.
Human Heredity|April 2, 2010
Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction testsMichael Steffens, Tim Becker, Thomas Sander, et al.
Neurology|November 2, 2014
A homozygous splice-site mutation in CARS2 is associated with progressive myoclonic epilepsyKerstin Hallmann, Gábor Zsurka, Susanna Moskau-Hartmann, et al.
Epilepsy Research|March 21, 2002
Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8qRobert Robinson, Nichole Taske, Thomas Sander, et al.
Epilepsia|January 15, 2014
A common SCN1A splice-site polymorphism modifies the effect of carbamazepine on cortical excitability--a pharmacogenetic transcranial magnetic stimulation studyKatja Menzler, Anke Hermsen, Katharina Balkenhol, et al.
Neurobiology of Disease|February 25, 2014
Exonic microdeletions of the gephyrin gene impair GABAergic synaptic inhibition in patients with idiopathic generalized epilepsyBorislav Dejanovic, Dennis Lal, Claudia B Catarino, et al.
Human Molecular Genetics|July 14, 2009
Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritanceLeanne M Dibbens, Saul Mullen, Ingo Helbig, et al.
Epilepsia|July 5, 2014
Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsyEva M Reinthaler, Dennis Lal, Wiktor Jurkowski, et al.
Pageof 14

Showing results (91-100 of 136) with videos related to

Sort By:
Pageof 14
European Archives of Psychiatry and Clinical Neuroscience|April 7, 2005
Polymorphisms in the NMDA subunit 2B are not associated with alcohol dependence and alcohol withdrawal-induced seizures and delirium tremensAndre Tadic, Norbert Dahmen, Armin Szegedi, et al.
Annals of Neurology|June 2, 2005
Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsyUlrike Tauer, Susanne Lorenz, Kirsten P Lenzen, et al.
Journal of Neurology|April 9, 2013
EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvementRoberta Biancheri, Denise Cassandrini, Francesca Pinto, et al.
Human Heredity|April 2, 2010
Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction testsMichael Steffens, Tim Becker, Thomas Sander, et al.
Neurology|November 2, 2014
A homozygous splice-site mutation in CARS2 is associated with progressive myoclonic epilepsyKerstin Hallmann, Gábor Zsurka, Susanna Moskau-Hartmann, et al.
Epilepsy Research|March 21, 2002
Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8qRobert Robinson, Nichole Taske, Thomas Sander, et al.
Epilepsia|January 15, 2014
A common SCN1A splice-site polymorphism modifies the effect of carbamazepine on cortical excitability--a pharmacogenetic transcranial magnetic stimulation studyKatja Menzler, Anke Hermsen, Katharina Balkenhol, et al.
Neurobiology of Disease|February 25, 2014
Exonic microdeletions of the gephyrin gene impair GABAergic synaptic inhibition in patients with idiopathic generalized epilepsyBorislav Dejanovic, Dennis Lal, Claudia B Catarino, et al.
Human Molecular Genetics|July 14, 2009
Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritanceLeanne M Dibbens, Saul Mullen, Ingo Helbig, et al.
Epilepsia|July 5, 2014
Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsyEva M Reinthaler, Dennis Lal, Wiktor Jurkowski, et al.
Pageof 14