Sander T - Search Results

1

Mutation analysis of the hyperpolarization-activated cyclic nucleotide-gated channels HCN1 and HCN2 in idiopathic generalized epilepsy.

Tang B, Sander T, Craven KB, Hempelmann A, Escayg A. Tang B, et al. Among authors: sander t. Neurobiol Dis. 2008 Jan;29(1):59-70. doi: 10.1016/j.nbd.2007.08.006. Epub 2007 Aug 24. Neurobiol Dis. 2008. PMID: 17931874 Free PMC article.

2

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

3

A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy.

Escayg A, Heils A, MacDonald BT, Haug K, Sander T, Meisler MH. Escayg A, et al. Among authors: sander t. Am J Hum Genet. 2001 Apr;68(4):866-73. doi: 10.1086/319524. Epub 2001 Mar 14. Am J Hum Genet. 2001. PMID: 11254445 Free PMC article.

4

Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4.

von Brevern M, Ta N, Shankar A, Wiste A, Siegel A, Radtke A, Sander T, Escayg A. von Brevern M, et al. Among authors: sander t. Headache. 2006 Jul-Aug;46(7):1136-41. doi: 10.1111/j.1526-4610.2006.00504.x. Headache. 2006. PMID: 16866717

5

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

6

Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.

Escayg A, De Waard M, Lee DD, Bichet D, Wolf P, Mayer T, Johnston J, Baloh R, Sander T, Meisler MH. Escayg A, et al. Among authors: sander t. Am J Hum Genet. 2000 May;66(5):1531-9. doi: 10.1086/302909. Epub 2000 Apr 4. Am J Hum Genet. 2000. PMID: 10762541 Free PMC article.

7

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.

8

Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy.

Lenzen KP, Heils A, Lorenz S, Hempelmann A, Höfels S, Lohoff FW, Schmitz B, Sander T. Lenzen KP, et al. Among authors: sander t. Epilepsy Res. 2005 Feb;63(2-3):113-8. doi: 10.1016/j.eplepsyres.2005.01.002. Epilepsy Res. 2005. PMID: 15725393

9

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

10

Myofibrillogenesis regulator 1 gene (MR-1) mutation in an Omani family with paroxysmal nonkinesigenic dyskinesia.

Hempelmann A, Kumar S, Muralitharan S, Sander T. Hempelmann A, et al. Among authors: sander t. Neurosci Lett. 2006 Jul 10;402(1-2):118-20. doi: 10.1016/j.neulet.2006.03.048. Epub 2006 Apr 24. Neurosci Lett. 2006. PMID: 16632198

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