Sander T - Search Results

1

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

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

Association analysis of malic enzyme 2 gene polymorphisms with idiopathic generalized epilepsy.

Lenzen KP, Heils A, Lorenz S, Hempelmann A, Sander T. Lenzen KP, et al. Among authors: sander t. Epilepsia. 2005 Oct;46(10):1637-41. doi: 10.1111/j.1528-1167.2005.00270.x. Epilepsia. 2005. PMID: 16190936 Free article.

6

Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivity.

Lorenz S, Heils A, Taylor KP, Gehrmann A, Muhle H, Gresch M, Becker T, Tauer U, Stephani U, Sander T. Lorenz S, et al. Among authors: sander t. Neurosci Lett. 2006 Apr 24;397(3):234-9. doi: 10.1016/j.neulet.2005.12.030. Epub 2006 Jan 6. Neurosci Lett. 2006. PMID: 16406321

7

Allelic association of a truncation mutation of the KCNMB3 gene with idiopathic generalized epilepsy.

Lorenz S, Heils A, Kasper JM, Sander T. Lorenz S, et al. Among authors: sander t. Am J Med Genet B Neuropsychiatr Genet. 2007 Jan 5;144B(1):10-3. doi: 10.1002/ajmg.b.30369. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 16958040

8

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

9

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

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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