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American Journal of Medical Genetics
|
April 17, 1999
Evaluation of a putative major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q14
T Sander, H Schulz, A M Vieira-Saeker, et al.
Pharmacogenetics
|
August 1, 1997
Influence of the dopamine D2 receptor (DRD2) genotype on neuroadaptive effects of alcohol and the clinical outcome of alcoholism
U Finckh, H Rommelspacher, S Kuhn, et al.
American Journal of Medical Genetics
|
February 16, 1996
Common subtypes of idiopathic generalized epilepsies: lack of linkage to D20S19 close to candidate loci (EBN1, EEGV1) on chromosome 20
T Sander, T Hildmann, T F Wienker, et al.
Acta Neurologica Scandinavica
|
July 1, 1997
Linkage analysis between idiopathic generalized epilepsies and the GABA(A) receptor alpha5, beta3 and gamma3 subunit gene cluster on chromosome 15
T Sander, R Kretz, M P Williamson, et al.
Psychiatric Genetics
|
April 28, 2001
Exonic variants of the GABA(B) receptor gene and panic disorder
P G Sand, C Godau, P Riederer, et al.
Epilepsy Research
|
April 1, 1996
Exclusion of linkage between idiopathic generalized epilepsies and the GABAA receptor alpha 1 and gamma 2 subunit gene cluster on chromosome 5
T Sander, T Hildmann, D Janz, et al.
Epilepsy Research
|
May 4, 2004
Association between variation in the human KCNJ10 potassium ion channel gene and seizure susceptibility
R J Buono, F W Lohoff, T Sander, et al.
Mededportal : the Journal of Teaching and Learning Resources
|
June 25, 2025
Peer-to-Peer Mental Health Training: A National Model for Peer Support for Medical and Dental Students
Armand Amini, Avina Rami, Rhea W Teng, et al.
Physics in Medicine and Biology
|
October 7, 2017
A multicentre audit of HDR/PDR brachytherapy absolute dosimetry in association with the INTERLACE trial (NCT015662405)
P Díez, E G A Aird, T Sander, et al.
Epilepsy Research
|
September 28, 2002
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures
C Windemuth, H Schulz, K Saar, et al.
Page
of 13
Search research articles
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Showing results (111-120 of 124) with videos related to
Sort By:
Page
of 13
American Journal of Medical Genetics
|
April 17, 1999
Evaluation of a putative major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q14
T Sander, H Schulz, A M Vieira-Saeker, et al.
Pharmacogenetics
|
August 1, 1997
Influence of the dopamine D2 receptor (DRD2) genotype on neuroadaptive effects of alcohol and the clinical outcome of alcoholism
U Finckh, H Rommelspacher, S Kuhn, et al.
American Journal of Medical Genetics
|
February 16, 1996
Common subtypes of idiopathic generalized epilepsies: lack of linkage to D20S19 close to candidate loci (EBN1, EEGV1) on chromosome 20
T Sander, T Hildmann, T F Wienker, et al.
Acta Neurologica Scandinavica
|
July 1, 1997
Linkage analysis between idiopathic generalized epilepsies and the GABA(A) receptor alpha5, beta3 and gamma3 subunit gene cluster on chromosome 15
T Sander, R Kretz, M P Williamson, et al.
Psychiatric Genetics
|
April 28, 2001
Exonic variants of the GABA(B) receptor gene and panic disorder
P G Sand, C Godau, P Riederer, et al.
Epilepsy Research
|
April 1, 1996
Exclusion of linkage between idiopathic generalized epilepsies and the GABAA receptor alpha 1 and gamma 2 subunit gene cluster on chromosome 5
T Sander, T Hildmann, D Janz, et al.
Epilepsy Research
|
May 4, 2004
Association between variation in the human KCNJ10 potassium ion channel gene and seizure susceptibility
R J Buono, F W Lohoff, T Sander, et al.
Mededportal : the Journal of Teaching and Learning Resources
|
June 25, 2025
Peer-to-Peer Mental Health Training: A National Model for Peer Support for Medical and Dental Students
Armand Amini, Avina Rami, Rhea W Teng, et al.
Physics in Medicine and Biology
|
October 7, 2017
A multicentre audit of HDR/PDR brachytherapy absolute dosimetry in association with the INTERLACE trial (NCT015662405)
P Díez, E G A Aird, T Sander, et al.
Epilepsy Research
|
September 28, 2002
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures
C Windemuth, H Schulz, K Saar, et al.
Page
of 13