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Plos One
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January 21, 2016
Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation Sequencing
Dennis Lal, Bernd A Neubauer, Mohammad R Toliat, et al.
Journal of Neuropathology and Experimental Neurology
|
November 16, 2011
Promoter variants determine γ-aminobutyric acid homeostasis-related gene transcription in human epileptic hippocampi
Katharina Pernhorst, Anna Raabe, Pitt Niehusmann, et al.
Journal of Cognitive Neuroscience
|
November 21, 2009
Ebbinghaus revisited: influences of the BDNF Val66Met polymorphism on backward serial recall are modulated by human aging
Shu-Chen Li, Christian Chicherio, Lars Nyberg, et al.
Psychopharmacology
|
November 17, 2010
Lack of association between 71 variations located in candidate genes and response to acute haloperidol treatment
Ina Giegling, Antonio Drago, Martin Schäfer, et al.
Brain Research
|
January 22, 2013
Rs6295 promoter variants of the serotonin type 1A receptor are differentially activated by c-Jun in vitro and correlate to transcript levels in human epileptic brain tissue
Katharina Pernhorst, Karen M J van Loo, Marec von Lehe, et al.
Neuromolecular Medicine
|
June 25, 2010
Association study of TRPC4 as a candidate gene for generalized epilepsy with photosensitivity
Sarah von Spiczak, Hiltrud Muhle, Ingo Helbig, et al.
Pharmacogenetics and Genomics
|
September 23, 2010
Glutamatergic gene variants impact the clinical profile of efficacy and side effects of haloperidol
Ina Giegling, Antonio Drago, Vita Dolžan, et al.
Annals of Neurology
|
May 1, 2014
Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsy
Nicola Vanni, Floriana Fruscione, Edoardo Ferlazzo, et al.
Plos One
|
September 17, 2013
RBFOX1 and RBFOX3 mutations in rolandic epilepsy
Dennis Lal, Eva M Reinthaler, Janine Altmüller, et al.
Epilepsy Research
|
March 27, 2010
Role of GRM4 in idiopathic generalized epilepsies analysed by genetic association and sequence analysis
Hiltrud Muhle, Sarah von Spiczak, Verena Gaus, et al.
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of 14
Search research articles
Search
Showing results (81-90 of 136) with videos related to
Sort By:
Page
of 14
Plos One
|
January 21, 2016
Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation Sequencing
Dennis Lal, Bernd A Neubauer, Mohammad R Toliat, et al.
Journal of Neuropathology and Experimental Neurology
|
November 16, 2011
Promoter variants determine γ-aminobutyric acid homeostasis-related gene transcription in human epileptic hippocampi
Katharina Pernhorst, Anna Raabe, Pitt Niehusmann, et al.
Journal of Cognitive Neuroscience
|
November 21, 2009
Ebbinghaus revisited: influences of the BDNF Val66Met polymorphism on backward serial recall are modulated by human aging
Shu-Chen Li, Christian Chicherio, Lars Nyberg, et al.
Psychopharmacology
|
November 17, 2010
Lack of association between 71 variations located in candidate genes and response to acute haloperidol treatment
Ina Giegling, Antonio Drago, Martin Schäfer, et al.
Brain Research
|
January 22, 2013
Rs6295 promoter variants of the serotonin type 1A receptor are differentially activated by c-Jun in vitro and correlate to transcript levels in human epileptic brain tissue
Katharina Pernhorst, Karen M J van Loo, Marec von Lehe, et al.
Neuromolecular Medicine
|
June 25, 2010
Association study of TRPC4 as a candidate gene for generalized epilepsy with photosensitivity
Sarah von Spiczak, Hiltrud Muhle, Ingo Helbig, et al.
Pharmacogenetics and Genomics
|
September 23, 2010
Glutamatergic gene variants impact the clinical profile of efficacy and side effects of haloperidol
Ina Giegling, Antonio Drago, Vita Dolžan, et al.
Annals of Neurology
|
May 1, 2014
Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsy
Nicola Vanni, Floriana Fruscione, Edoardo Ferlazzo, et al.
Plos One
|
September 17, 2013
RBFOX1 and RBFOX3 mutations in rolandic epilepsy
Dennis Lal, Eva M Reinthaler, Janine Altmüller, et al.
Epilepsy Research
|
March 27, 2010
Role of GRM4 in idiopathic generalized epilepsies analysed by genetic association and sequence analysis
Hiltrud Muhle, Sarah von Spiczak, Verena Gaus, et al.
Page
of 14