Browse by Journal Title

2010

Whole-genome linkage scan for epilepsy-related photosensitivity: a mega-analysis.
de Kovel, C.G. and Pinto, D. and Tauer, U. and Lorenz, S. and Muhle, H. and Leu, C. and Neubauer, B.A. and Hempelmann, A. and Callenbach, P.M. and Scheffer, I.E. and Berkovic, S.F. and Rudolf, G. and Striano, P. and Siren, A. and Baykan, B. and Sander, T. and Lindhout, D. and Kasteleijn-Nolst Trenite, D.G. and Stephani, U. and Koeleman, B.P.
Epilepsy Research 89 (2-3): 286-294. May 2010

2007

Linkage and mutational analysis of CLCN2 in childhood absence epilepsy.
Everett, K. and Chioza, B. and Aicardi, J. and Aschauer, H. and Brouwer, O. and Callenbach, P. and Covanis, A. and Dooley, J. and Dulac, O. and Durner, M. and Eeg-Olofsson, O. and Feucht, M. and Friis, M. and Guerrini, R. and Heils, A. and Kjeldsen, M. and Nabbout, R. and Sander, T. and Wirrell, E. and McKeigue, P. and Robinson, R. and Taske, N. and Gardiner, M.
Epilepsy Research 75 (2-3): 145-153. July 2007

Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy.
Hempelmann, A. and Cobilanschi, J. and Heils, A. and Muhle, H. and Stephani, U. and Weber, Y. and Lerche, H. and Sander, T.
Epilepsy Research 74 (1): 28-32. April 2007

2006

Confirmatory evidence for an association of the connexin-36 gene with juvenile myoclonic epilepsy.
Hempelmann, A. and Heils, A. and Sander, T.
Epilepsy Research 71 (2-3): 223-228. October 2006

Evaluation of CACNA1H in European patients with childhood absence epilepsy.
Chioza, B. and Everett, K. and Aschauer, H. and Brouwer, O. and Callenbach, P. and Covanis, A. and Dulac, O. and Durner, M. and Eeg-Olofsson, O. and Feucht, M. and Friis, M. and Heils, A. and Kjeldsen, M. and Larsson, K. and Lehesjoki, A.E. and Nabbout, R. and Olsson, I. and Sander, T. and Siren, A. and Robinson, R. and Rees, M. and Gardiner, R.M.
Epilepsy Research 69 (2): 177-181. May 2006

2005

A new EF-hand containing gene EFHC2 on Xp11.4: Tentative evidence for association with juvenile myoclonic epilepsy.
Gu, W. and Sander, T. and Heils, A. and Lenzen, K.P. and Steinlein, O.K.
Epilepsy Research 66 (1-3): 91-98. 18 August 2005

Functional GABA uptake at inhibitory synapses in CA1 of chronically epileptic rats.
Stief, F. and Piechotta, A. and Gabriel, S. and Schmitz, D. and Draguhn, A.
Epilepsy Research 66 (1-3): 199-202. August 2005

Neonatal seizures with tonic clonic sequences and poor developmental outcome.
Schmitt, B. and Wohlrab, G. and Sander, T. and Steinlein, O.K. and Hajnal, B.L.
Epilepsy Research 65 (3): 161-168. 1 July 2005

Association analysis of the Arg220His variation of the human gene encoding the GABA delta subunit with idiopathic generalized epilepsy.
Lenzen, K.P. and Heils, A. and Lorenz, S. and Hempelmann, A. and Sander, T.
Epilepsy Research 65 (1-2): 53-57. June 2005

Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy.
Lenzen, K.P. and Heils, A. and Lorenz, S. and Hempelmann, A. and Hoefels, S. and Lohoff, F.W. and Schmitz, B. and Sander, T.
Epilepsy Research 63 (2): 113-118. 1 January 2005

2004

Association between variation in the human KCNJ10 potassium ion channel gene and seizure susceptibility.
Buono, R.J. and Lohoff, F.W. and Sander, T. and Sperling, M.R. and O'Connor, M.J. and Dlugos, D.J. and Ryan, S.G. and Golden, G.T. and Zhao, H. and Scattergood, T.M. and Berrettini, W.H. and Ferraro, T.N.
Epilepsy Research 58 (2-3): 175-183. February 2004

2002

Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy.
Sander, T. and Toliat, M.R. and Heils, A. and Leschik, G. and Becker, C. and Rueschendorf, F. and Rohde, K. and Mundlos, S. and Nuernberg, P.
Epilepsy Research 51 (3): 249-255. 1 October 2002

No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures.
Windemuth, C. and Schulz, H. and Saar, K. and Gennaro, E. and Bianchi, A. and Zara, F. and Bulteau, C. and Kaminska, A. and Ville, D. and Cieuta, C. and Nabbout-Tarantino, R. and Prud'homme, J.F. and Dulac, O. and Bate, L. and Gardiner, R.M. and Lindhout, D. and Wienker, T.F. and Janz, D. and Sander, T.
Epilepsy Research 51 (1-2): 23-29. 1 September 2002

Linkage analysis between childhood absence epilepsy and genes encoding GABAAand GABA Breceptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q.
Robinson, R. and Taske, N. and Sander, T. and Heils, A. and Whitehouse, W. and Goutieres, F. and Aicardi, J. and Lehesjoki, A.E. and Siren, A. and Friis, M.L. and Kjeldsen, M.J. and Panayiotopoulos, C. and Kennedy, C. and Ferrie, C. and Rees, M. and Gardiner, R.M.
Epilepsy Research 48 : 169-179. 1 February 2002

Failure to replicate an allelic association between an exon 8 polymorphism of the human alpha1A calcium channel gene and common syndromes of idiopathic generalized epilepsy.
Sander, T. and Toliat, M.R. and Heils, A. and Becker, C. and Nuernberg, P.
Epilepsy Research 49 (2): 173-177. 1 January 2002

2001

Mutation analysis of the potassium chloride cotransporter KCC3 (SLC12A6) in rolandic and idiopathic generalized epilepsy.
Steinlein, O.K. and Neubauer, B.A. and Sander, T. and Song, L. and Stoodt, J. and Mount, D.B.
Epilepsy Research 44 : 191-195. 1 May 2001

2000

No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy.
Haug, K. and Hallmann, K. and Horvath, S. and Sander, T. and Kubisch, C. and Rau, B. and Dullinger, J. and Beyenburg, S. and Elger, C.E. and Propping, P. and Heils, A.
Epilepsy Research 42 : 57-62. 1 November 2000

Variation of the genes encoding the human glutamate EAAT2, serotonin and dopamine transporters and susceptibility to idiopathic generalized epilepsy.
Sander, T. and Berlin, W. and Ostapowicz, A. and Samochowiec, J. and Gscheidel, N. and Hoehe, M.R.
Epilepsy Research 41 (1): 75-81. 1 August 2000

Association analysis between a regulatory-promoter polymorphism of the human monoamine oxidase A gene and idiopathic generalized epilepsy.
Haug, K. and Sander, T. and Hallmann, K. and Lentze, M.J. and Propping, P. and Elger, C.E. and Heils, A.
Epilepsy Research 39 : 127-132. 1 April 2000

Genetic variation of the human mu-opioid receptor and susceptibility to idiopathic absence epilepsy.
Sander, T. and Berlin, W. and Gscheidel, N. and Wendel, B. and Janz, D. and Hoehe, M.R.
Epilepsy Research 39 (1): 57-61. 1 March 2000

1998

Interaction between superficial layers of the entorhinal cortex and the hippocampus in normal and epileptic temporal lobe.
Gloveli, T. and Schmitz, D. and Heinemann, U.
Epilepsy Research 32 (1-2): 183-193. September 1998

The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy.
Sander, T. and Peters, C. and Janz, D. and Bianchi, A. and Bauer, G. and Wienker, T.F. and Hildmann, T. and Epplen, J.T. and Riess, O.
Epilepsy Research 29 : 115-122. 1 January 1998

1996

Exclusion of linkage between idiopathic generalized epilepsies and the GABAA receptor alpha1 and gamma2 subunit gene cluster on chromosome 5.
Sander, T. and Hildmann, T. and Janz, D. and Wienker, T.F. and Bianchi, A. and Bauer, G. and Sailer, U. and Scaramelli, A. and Neitzel, H. and Schmitz, B. and Bailey, M.E.S. and Beckmannagetta, G. and Johnson, K.J. and Darlison, M.G.
Epilepsy Research 23 (3): 235-244. 1 January 1996