AAAAAA
Results: 1-25/35
Authors:
Steinlein, OK
Neubauer, BA
Sander, T
Song, LY
Stoodt, J
Mount, DB
Citation: Ok. Steinlein et al., Mutation analysis of the potassium chloride cotransporter KCC3 (SLC12A6) in rolandic and idiopathic generalized epilepsy, EPILEPSY R, 44(2-3), 2001, pp. 191-195
Authors:
Sobetzko, D
Sander, T
Becker, CM
Citation: D. Sobetzko et al., Genetic variation of the human glycine receptor subunit genes GLRA3 and GLRB and susceptibility to idiopathic generalized epilepsies, AM J MED G, 105(6), 2001, pp. 534-538
Authors:
Escayg, A
Heils, A
MacDonald, BT
Haug, K
Sander, T
Meisler, MH
Citation: A. Escayg et al., A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus - and prevalence of variants in patients with epilepsy, AM J HU GEN, 68(4), 2001, pp. 866-873
Authors:
Franke, P
Nothen, MM
Wang, T
Knapp, M
Lichtermann, D
Neidt, H
Sander, T
Propping, P
Maier, W
Citation: P. Franke et al., DRD4 exon IIIVNTR polymorphism-susceptibility factor for heroin dependence? Results of a case-control and a family-based association approach, MOL PSYCHI, 5(1), 2000, pp. 101-104
Authors:
Franke, P
Wang, T
Nothen, MM
Knapp, M
Neith, H
Lichtermann, D
Zur Capellen, KM
Sander, T
Propping, P
Maier, W
Citation: P. Franke et al., Susceptibility for alcoholism: DRD4 exon III polymorphism: a case-control and a family-based association approach, ADDICT BIOL, 5(3), 2000, pp. 289-295
Authors:
Sander, T
Ostapowicz, A
Samochowiec, J
Smolka, M
Rommelspacher, H
Winterer, G
Schmidt, LG
Citation: T. Sander et al., Evaluation of an allelic association of the serotonin 5-HT1B G681C polymorphism with antisocial alcoholism in the German population, ADDICT BIOL, 5(2), 2000, pp. 167-172
Authors:
O'Brien, M
Lamperti, P
Williams, T
Sander, T
Citation: M. O'Brien et al., Comparison of the NIST and NPL air Kerma standards used for X-ray measurements between 10 kV and 80 kV (vol 105, pg 701, 2000), J RES NAT I, 105(6), 2000, pp. 901-902
Authors:
Sander, T
Schulz, H
Saar, K
Gennaro, E
Riggio, MC
Bianchi, A
Zara, F
Luna, D
Bulteau, C
Kaminska, A
Ville, D
Cieuta, C
Picard, F
Prud'homme, JF
Bate, L
Sundquist, A
Gardiner, RM
Janssen, GAMAJ
de Haan, GJ
Kasteleijn-Nolst-Trenite, DGA
Bader, A
Lindhout, D
Riess, O
Wienker, TF
Janz, D
Reis, A
Citation: T. Sander et al., Genome search for susceptibility loci of common idiopathic generalised epilepsies, HUM MOL GEN, 9(10), 2000, pp. 1465-1472
Authors:
Sander, T
Konig, S
Rothe, GM
Janssen, A
Weisgerber, H
Citation: T. Sander et al., Genetic variation of European beech (Fagus sylvatica L.) along an altitudinal transect at mount Vogelsberg in Hesse, Germany, MOL ECOL, 9(9), 2000, pp. 1349-1361
Authors:
Haug, K
Sander, T
Hallmann, K
Rau, B
Dullinger, JS
Elger, CE
Propping, P
Heils, A
Citation: K. Haug et al., The voltage-gated sodium channel beta 2-subunit gene and idiopathic generalized epilepsy, NEUROREPORT, 11(12), 2000, pp. 2687-2689
Authors:
Schmidt, LG
Sander, T
Citation: Lg. Schmidt et T. Sander, Genetics of alcohol withdrawal, EUR PSYCHIA, 15(2), 2000, pp. 135-139
Authors:
Haug, K
Hallmann, K
Horvath, S
Sander, T
Kubisch, C
Rau, B
Dullinger, J
Beyenburg, S
Elger, CE
Propping, P
Heils, A
Citation: K. Haug et al., No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy, EPILEPSY R, 42(1), 2000, pp. 57-62
Authors:
Sander, T
Berlin, W
Ostapowicz, A
Samochowiec, J
Gscheidel, N
Hoehe, MR
Citation: T. Sander et al., Variation of the genes encoding the human glutamate EAAT2, serotonin and dopamine transporters and susceptibility to idiopathic generalized epilepsy, EPILEPSY R, 41(1), 2000, pp. 75-81
Authors:
Haug, K
Sander, T
Hallmann, K
Lentze, MJ
Propping, P
Elger, CE
Heils, A
Citation: K. Haug et al., Association analysis between a regulatory-promoter polymorphism of the human monoamine oxidase A gene and idiopathic generalized epilepsy, EPILEPSY R, 39(2), 2000, pp. 127-132
Authors:
Sander, T
Berlin, W
Gscheidel, N
Wendel, B
Janz, D
Hoehe, MR
Citation: T. Sander et al., Genetic variation of the human mu-opioid receptor and susceptibility to idiopathic absence epilepsy, EPILEPSY R, 39(1), 2000, pp. 57-61
Authors:
Haug, K
Kremerskothen, J
Hallmann, K
Sander, T
Dullinger, J
Rau, B
Beyenburg, S
Lentze, MJ
Barnekow, A
Elger, CE
Propping, P
Heils, A
Citation: K. Haug et al., Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy, MOL CELL PR, 14(4), 2000, pp. 255-260
Authors:
Winterer, G
Smolka, M
Samochowiec, J
Mulert, C
Ziller, M
Mahlberg, R
Wuebben, Y
Gallinat, J
Rommelspacher, H
Herrmann, WM
Sander, T
Citation: G. Winterer et al., Association analysis of GABA(A) beta 2 and gamma 2 gene polymorphisms withevent-related prefrontal activity in man, HUM GENET, 107(5), 2000, pp. 513-518
Authors:
Schmidt, LG
Sander, T
Kuhn, S
Smolka, M
Rommelspacher, H
Samochowiec, J
Lesch, KP
Citation: Lg. Schmidt et al., Different allele distribution of a regulatory MAOA gene promoter polymorphism in antisocial and anxious-depressive alcoholics, J NEURAL TR, 107(6), 2000, pp. 681-689
Authors:
Hallmann, K
Durner, M
Sander, T
Steinlein, OK
Citation: K. Hallmann et al., Mutation analysis of the inwardly rectifying K+ channels KCNJ6 (GIRK2) andKCNJ3 (GIRK1) in juvenile myoclonic epilepsy, AM J MED G, 96(1), 2000, pp. 8-11
Authors:
Gasser, T
Dichgans, M
Jurkat-Rott, K
Klockgether, T
Klopstock, T
Kretzschmar, H
Lehmann-Horn, F
Reichmann, H
Rolfs, A
Sander, T
Stogbauer, F
Citation: T. Gasser et al., Molecular diagnosis of hereditary neurological diseases. A position paper, NERVENARZT, 71(10), 2000, pp. 774-796
High pressure optical and X-ray diffraction studies of two polymorphs of K(RE)P2Se6 (RE = Pr and Tb)
Authors:
Orgzall, I
Lorenz, B
Dorhout, PK
Van Calcar, PM
Brister, K
Sander, T
Hochheimer, HD
Citation: I. Orgzall et al., High pressure optical and X-ray diffraction studies of two polymorphs of K(RE)P2Se6 (RE = Pr and Tb), J PHYS CH S, 61(1), 2000, pp. 123-134
Authors:
Escayg, A
De Waard, M
Lee, DD
Bichet, D
Wolf, P
Mayer, T
Johnston, J
Baloh, R
Sander, T
Meisler, MH
Citation: A. Escayg et al., Coding and noncoding variation of the human calcium-channel beta(4)-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodicataxia, AM J HU GEN, 66(5), 2000, pp. 1531-1539
Authors:
Samochowiec, J
Rottmann, M
Okladnova, O
Syagailo, Y
Stober, G
Sander, T
Muhlbauer, E
Smolka, M
Tranitz, M
Winterer, G
Rommelspacher, H
Schmidt, LG
Lesch, KP
Citation: J. Samochowiec et al., Association analysis of a PAX-6 gene promoter-associated polymorphic repeat with alcohol dependence, ADDICT BIOL, 4(3), 1999, pp. 323-328
Authors:
Steinlein, OK
Stoodt, J
Biervert, C
Janz, D
Sander, T
Citation: Ok. Steinlein et al., The voltage gated potassium channel KCNQ2 and idiopathic generalized epilepsy, NEUROREPORT, 10(6), 1999, pp. 1163-1166
Authors:
Sander, T
Syagailo, Y
Samochowiec, J
Okladnova, O
Lesch, KP
Janz, D
Citation: T. Sander et al., Association analysis of a regulatory promoter polymorphism of the PAX-6 gene with idiopathic generalized epilepsy, EPILEPSY R, 36(1), 1999, pp. 61-67