Sander T - Search Results

1

Association analysis between a regulatory-promoter polymorphism of the human monoamine oxidase A gene and idiopathic generalized epilepsy.

Haug K, Sander T, Hallmann K, Lentze MJ, Propping P, Elger CE, Heils A. Haug K, et al. Among authors: sander t. Epilepsy Res. 2000 Apr;39(2):127-32. doi: 10.1016/s0920-1211(99)00116-3. Epilepsy Res. 2000. PMID: 10759301

2

Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy.

Sander T, Toliat MR, Heils A, Leschik G, Becker C, Rüschendorf F, Rohde K, Mundlos S, Nürnberg P. Sander T, et al. Epilepsy Res. 2002 Oct;51(3):249-55. doi: 10.1016/s0920-1211(02)00152-3. Epilepsy Res. 2002. PMID: 12399075

3

Association analysis of the Arg220His variation of the human gene encoding the GABA delta subunit with idiopathic generalized epilepsy.

Lenzen KP, Heils A, Lorenz S, Hempelmann A, Sander T. Lenzen KP, et al. Among authors: sander t. Epilepsy Res. 2005 Jun;65(1-2):53-7. doi: 10.1016/j.eplepsyres.2005.04.005. Epilepsy Res. 2005. PMID: 16023832

4

A new EF-hand containing gene EFHC2 on Xp11.4: tentative evidence for association with juvenile myoclonic epilepsy.

Gu W, Sander T, Heils A, Lenzen KP, Steinlein OK. Gu W, et al. Among authors: sander t. Epilepsy Res. 2005 Aug-Sep;66(1-3):91-8. doi: 10.1016/j.eplepsyres.2005.07.003. Epilepsy Res. 2005. PMID: 16112844

5

Confirmatory evidence for an association of the connexin-36 gene with juvenile myoclonic epilepsy.

Hempelmann A, Heils A, Sander T. Hempelmann A, et al. Among authors: sander t. Epilepsy Res. 2006 Oct;71(2-3):223-8. doi: 10.1016/j.eplepsyres.2006.06.021. Epub 2006 Jul 28. Epilepsy Res. 2006. PMID: 16876983

6

Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy.

Hempelmann A, Cobilanschi J, Heils A, Muhle H, Stephani U, Weber Y, Lerche H, Sander T. Hempelmann A, et al. Among authors: sander t. Epilepsy Res. 2007 Apr;74(1):28-32. doi: 10.1016/j.eplepsyres.2006.12.001. Epub 2007 Jan 9. Epilepsy Res. 2007. PMID: 17215107

7

Role of GRM4 in idiopathic generalized epilepsies analysed by genetic association and sequence analysis.

Muhle H, von Spiczak S, Gaus V, Kara S, Helbig I, Hampe J, Franke A, Weber Y, Lerche H, Kleefuss-Lie AA, Elger CE, Schreiber S, Stephani U, Sander T. Muhle H, et al. Among authors: sander t. Epilepsy Res. 2010 May;89(2-3):319-26. doi: 10.1016/j.eplepsyres.2010.02.004. Epub 2010 Mar 24. Epilepsy Res. 2010. PMID: 20338729

8

Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy.

Haug K, Kremerskothen J, Hallmann K, Sander T, Dullinger J, Rau B, Beyenburg S, Lentze MJ, Barnekow A, Elger CE, Propping P, Heils A. Haug K, et al. Among authors: sander t. Mol Cell Probes. 2000 Aug;14(4):255-60. doi: 10.1006/mcpr.2000.0314. Mol Cell Probes. 2000. PMID: 10970730

9

The voltage-gated sodium channel beta2-subunit gene and idiopathic generalized epilepsy.

Haug K, Sander T, Hallmann K, Rau B, Dullinger JS, Elger CE, Propping P, Heils A. Haug K, et al. Among authors: sander t. Neuroreport. 2000 Aug 21;11(12):2687-9. doi: 10.1097/00001756-200008210-00016. Neuroreport. 2000. PMID: 10976944

10

No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy.

Haug K, Hallmann K, Horvath S, Sander T, Kubisch C, Rau B, Dullinger J, Beyenburg S, Elger CE, Propping P, Heils A. Haug K, et al. Among authors: sander t. Epilepsy Res. 2000 Nov;42(1):57-62. doi: 10.1016/s0920-1211(00)00164-9. Epilepsy Res. 2000. PMID: 10996506 Clinical Trial.

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