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Acta Neurologica Scandinavica. Supplementum
|
January 1, 1992
In search for genes predisposing to epilepsy: motives and methods
D Lindhout, T Sander, D J Halley, et al.
American Journal of Medical Genetics
|
October 28, 1997
Dopamine D4 receptor exon III alleles and variation of novelty seeking in alcoholics
T Sander, H Harms, P Dufeu, et al.
American Journal of Medical Genetics
|
April 17, 1999
Association analysis between a Cys23Ser substitution polymorphism of the human 5-HT2c receptor gene and neuronal hyperexcitability
J Samochowiec, M Smolka, G Winterer, et al.
Epilepsy Research
|
August 5, 2000
Variation of the genes encoding the human glutamate EAAT2, serotonin and dopamine transporters and Susceptibility to idiopathic generalized epilepsy
T Sander, W Berlin, A Ostapowicz, et al.
Pharmacopsychiatry
|
September 3, 2008
Gender-dependent association of a functional NGF polymorphism with anxiety-related personality traits
U E Lang, R Hellweg, M Bajbouj, et al.
Psychiatric Genetics
|
February 24, 2001
Genetic variation of the glutamate transporter EAAT2 gene and vulnerability to alcohol dependence
T Sander, A Ostapowicz, J Samochowiec, et al.
Alcoholism, Clinical and Experimental Research
|
May 11, 1999
Lack of an allelic association between polymorphisms of the dopamine D2 receptor gene and alcohol dependence in the German population
T Sander, M Ladehoff, J Samochowiec, et al.
Epilepsy Research
|
August 27, 1999
Association analysis of a regulatory promoter polymorphism of the PAX-6 gene with idiopathic generalized epilepsy
T Sander, Y Syagailo, J Samochowiec, et al.
Water Science and Technology : a Journal of the International Association on Water Pollution Research
|
November 24, 2004
Economic and environmental optimization of phosphorus removal
J Clauson-Kaas, T Sander Poulsen, B Neergaard-Jacobsen, et al.
Epilepsy Research
|
February 26, 2000
Genetic variation of the human mu-opioid receptor and susceptibility to idiopathic absence epilepsy
T Sander, W Berlin, N Gscheidel, et al.
Page
of 13
Search research articles
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Showing results (41-50 of 124) with videos related to
Sort By:
Page
of 13
Acta Neurologica Scandinavica. Supplementum
|
January 1, 1992
In search for genes predisposing to epilepsy: motives and methods
D Lindhout, T Sander, D J Halley, et al.
American Journal of Medical Genetics
|
October 28, 1997
Dopamine D4 receptor exon III alleles and variation of novelty seeking in alcoholics
T Sander, H Harms, P Dufeu, et al.
American Journal of Medical Genetics
|
April 17, 1999
Association analysis between a Cys23Ser substitution polymorphism of the human 5-HT2c receptor gene and neuronal hyperexcitability
J Samochowiec, M Smolka, G Winterer, et al.
Epilepsy Research
|
August 5, 2000
Variation of the genes encoding the human glutamate EAAT2, serotonin and dopamine transporters and Susceptibility to idiopathic generalized epilepsy
T Sander, W Berlin, A Ostapowicz, et al.
Pharmacopsychiatry
|
September 3, 2008
Gender-dependent association of a functional NGF polymorphism with anxiety-related personality traits
U E Lang, R Hellweg, M Bajbouj, et al.
Psychiatric Genetics
|
February 24, 2001
Genetic variation of the glutamate transporter EAAT2 gene and vulnerability to alcohol dependence
T Sander, A Ostapowicz, J Samochowiec, et al.
Alcoholism, Clinical and Experimental Research
|
May 11, 1999
Lack of an allelic association between polymorphisms of the dopamine D2 receptor gene and alcohol dependence in the German population
T Sander, M Ladehoff, J Samochowiec, et al.
Epilepsy Research
|
August 27, 1999
Association analysis of a regulatory promoter polymorphism of the PAX-6 gene with idiopathic generalized epilepsy
T Sander, Y Syagailo, J Samochowiec, et al.
Water Science and Technology : a Journal of the International Association on Water Pollution Research
|
November 24, 2004
Economic and environmental optimization of phosphorus removal
J Clauson-Kaas, T Sander Poulsen, B Neergaard-Jacobsen, et al.
Epilepsy Research
|
February 26, 2000
Genetic variation of the human mu-opioid receptor and susceptibility to idiopathic absence epilepsy
T Sander, W Berlin, N Gscheidel, et al.
Page
of 13