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Thomas Sander

Showing results (51-60 of 136) with videos related to

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Journal of Neural Transmission (Vienna, Austria : 1996)|November 4, 2009
Serotonin transporter promoter polymorphism and dopaminergic sensitivity in alcoholicsHenning Budde, Thomas Sander, Catrin Wernicke, et al.
Epilepsy Research|June 20, 2015
Juvenile myoclonic epilepsy: A system disorder of the brainPeter Wolf, Elza Márcia Targas Yacubian, Giuliano Avanzini, et al.
Headache|July 27, 2006
Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4Michael von Brevern, Nga Ta, Anupama Shankar, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 29, 2003
Candidate gene analysis of the human metabotropic glutamate receptor type 4 (GRM4) in patients with juvenile myoclonic epilepsyClaudia Izzi, Alessandro Barbon, Mohammad Reza Toliat, et al.
Biological Psychiatry|July 5, 2003
Association of the G1947A COMT (Val(108/158)Met) gene polymorphism with prefrontal P300 during information processingJürgen Gallinat, Malek Bajbouj, Thomas Sander, et al.
Chimia|October 27, 2017
The Screening Compound Collection: A Key Asset for Drug DiscoveryChristoph Boss, Julien Hazemann, Thierry Kimmerlin, et al.
Frontiers in Neurology|July 12, 2019
Linkage Evidence for a Two-Locus Inheritance of LQT-Associated Seizures in a Multigenerational LQT Family With a Novel <i>KCNQ1</i> Loss-of-Function MutationHarald Prüss, Guido Gessner, Stefan H Heinemann, et al.
Psychopharmacology|May 27, 2005
Association of a functional BDNF polymorphism and anxiety-related personality traitsUndine E Lang, Rainer Hellweg, Peter Kalus, et al.
Epilepsy Research|October 26, 2002
Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsyThomas Sander, Mohammad Reza Toliat, Armin Heils, et al.
Epilepsia|November 5, 2011
Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndromeHiltrud Muhle, Heather C Mefford, Tanja Obermeier, et al.
Pageof 14

Showing results (51-60 of 136) with videos related to

Sort By:
Pageof 14
Journal of Neural Transmission (Vienna, Austria : 1996)|November 4, 2009
Serotonin transporter promoter polymorphism and dopaminergic sensitivity in alcoholicsHenning Budde, Thomas Sander, Catrin Wernicke, et al.
Epilepsy Research|June 20, 2015
Juvenile myoclonic epilepsy: A system disorder of the brainPeter Wolf, Elza Márcia Targas Yacubian, Giuliano Avanzini, et al.
Headache|July 27, 2006
Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4Michael von Brevern, Nga Ta, Anupama Shankar, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 29, 2003
Candidate gene analysis of the human metabotropic glutamate receptor type 4 (GRM4) in patients with juvenile myoclonic epilepsyClaudia Izzi, Alessandro Barbon, Mohammad Reza Toliat, et al.
Biological Psychiatry|July 5, 2003
Association of the G1947A COMT (Val(108/158)Met) gene polymorphism with prefrontal P300 during information processingJürgen Gallinat, Malek Bajbouj, Thomas Sander, et al.
Chimia|October 27, 2017
The Screening Compound Collection: A Key Asset for Drug DiscoveryChristoph Boss, Julien Hazemann, Thierry Kimmerlin, et al.
Frontiers in Neurology|July 12, 2019
Linkage Evidence for a Two-Locus Inheritance of LQT-Associated Seizures in a Multigenerational LQT Family With a Novel <i>KCNQ1</i> Loss-of-Function MutationHarald Prüss, Guido Gessner, Stefan H Heinemann, et al.
Psychopharmacology|May 27, 2005
Association of a functional BDNF polymorphism and anxiety-related personality traitsUndine E Lang, Rainer Hellweg, Peter Kalus, et al.
Epilepsy Research|October 26, 2002
Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsyThomas Sander, Mohammad Reza Toliat, Armin Heils, et al.
Epilepsia|November 5, 2011
Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndromeHiltrud Muhle, Heather C Mefford, Tanja Obermeier, et al.
Pageof 14