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Neurology
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September 1, 1995
Refinement of map position of the human GluR6 kainate receptor gene (GRIK2) and lack of association and linkage with idiopathic generalized epilepsies
T Sander, D Janz, C Ramel, et al.
American Journal of Medical Genetics
|
July 25, 1997
Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphism
T Sander, T Hildmann, R Kretz, et al.
American Journal of Human Genetics
|
April 14, 2000
Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia
A Escayg, M De Waard, D D Lee, et al.
Human Genetics
|
January 5, 2001
Association analysis of GABAAbeta2 and gamma2 gene polymorphisms with event-related prefrontal activity in man
G Winterer, M Smolka, J Samochowiec, et al.
Alcoholism, Clinical and Experimental Research
|
September 1, 1996
Lack of allelic association of dopamine D1 and D2 (TaqIA) receptor gene polymorphisms with reduced dopaminergic sensitivity to alcoholism
A Heinz, T Sander, H Harms, et al.
Psychiatry Research
|
June 8, 1999
Association of a regulatory polymorphism in the promoter region of the monoamine oxidase A gene with antisocial alcoholism
J Samochowiec, K P Lesch, M Rottmann, et al.
Alcoholism, Clinical and Experimental Research
|
May 1, 1996
No association of the structural dopamine D2 receptor (DRD2) variant 311Cys with alcoholism
U Finckh, O von Widdern, M Giraldo-Velasquez, et al.
Epilepsy Research
|
September 21, 2000
No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy
K Haug, K Hallmann, S Horvath, et al.
American Journal of Medical Genetics
|
July 14, 1999
Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsy
T Sander, C Peters, G Kämmer, et al.
Der Nervenarzt
|
November 18, 2000
[Molecular diagnosis of hereditary neurologic diseases. Position paper]
T Gasser, M Dichgans, K Jurkat-Rott, et al.
Page
of 13
Search research articles
Search
Showing results (91-100 of 124) with videos related to
Sort By:
Page
of 13
Neurology
|
September 1, 1995
Refinement of map position of the human GluR6 kainate receptor gene (GRIK2) and lack of association and linkage with idiopathic generalized epilepsies
T Sander, D Janz, C Ramel, et al.
American Journal of Medical Genetics
|
July 25, 1997
Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphism
T Sander, T Hildmann, R Kretz, et al.
American Journal of Human Genetics
|
April 14, 2000
Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia
A Escayg, M De Waard, D D Lee, et al.
Human Genetics
|
January 5, 2001
Association analysis of GABAAbeta2 and gamma2 gene polymorphisms with event-related prefrontal activity in man
G Winterer, M Smolka, J Samochowiec, et al.
Alcoholism, Clinical and Experimental Research
|
September 1, 1996
Lack of allelic association of dopamine D1 and D2 (TaqIA) receptor gene polymorphisms with reduced dopaminergic sensitivity to alcoholism
A Heinz, T Sander, H Harms, et al.
Psychiatry Research
|
June 8, 1999
Association of a regulatory polymorphism in the promoter region of the monoamine oxidase A gene with antisocial alcoholism
J Samochowiec, K P Lesch, M Rottmann, et al.
Alcoholism, Clinical and Experimental Research
|
May 1, 1996
No association of the structural dopamine D2 receptor (DRD2) variant 311Cys with alcoholism
U Finckh, O von Widdern, M Giraldo-Velasquez, et al.
Epilepsy Research
|
September 21, 2000
No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy
K Haug, K Hallmann, S Horvath, et al.
American Journal of Medical Genetics
|
July 14, 1999
Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsy
T Sander, C Peters, G Kämmer, et al.
Der Nervenarzt
|
November 18, 2000
[Molecular diagnosis of hereditary neurologic diseases. Position paper]
T Gasser, M Dichgans, K Jurkat-Rott, et al.
Page
of 13