Lerche H - Search Results

1

Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1.

Suls A, Mullen SA, Weber YG, Verhaert K, Ceulemans B, Guerrini R, Wuttke TV, Salvo-Vargas A, Deprez L, Claes LR, Jordanova A, Berkovic SF, Lerche H, De Jonghe P, Scheffer IE. Suls A, et al. Among authors: lerche h. Ann Neurol. 2009 Sep;66(3):415-9. doi: 10.1002/ana.21724. Ann Neurol. 2009. PMID: 19798636

2

The new anticonvulsant retigabine favors voltage-dependent opening of the Kv7.2 (KCNQ2) channel by binding to its activation gate.

Wuttke TV, Seebohm G, Bail S, Maljevic S, Lerche H. Wuttke TV, et al. Among authors: lerche h. Mol Pharmacol. 2005 Apr;67(4):1009-17. doi: 10.1124/mol.104.010793. Epub 2005 Jan 20. Mol Pharmacol. 2005. PMID: 15662042

3

Ion channel defects in idiopathic epilepsies.

Lerche H, Weber YG, Jurkat-Rott K, Lehmann-Horn F. Lerche H, et al. Curr Pharm Des. 2005;11(21):2737-52. doi: 10.2174/1381612054546815. Curr Pharm Des. 2005. PMID: 16101452 Review.

4

Epileptic nystagmus: two case reports, clinical and pathophysiological review of the literature.

Weber YG, Roesche J, Lerche H. Weber YG, et al. Among authors: lerche h. J Neurol. 2006 Jun;253(6):767-71. doi: 10.1007/s00415-006-0114-2. Epub 2006 Mar 6. J Neurol. 2006. PMID: 16511649 Review.

5

Immunohistochemical analysis of KCNQ3 potassium channels in mouse brain.

Geiger J, Weber YG, Landwehrmeyer B, Sommer C, Lerche H. Geiger J, et al. Among authors: lerche h. Neurosci Lett. 2006 May 29;400(1-2):101-4. doi: 10.1016/j.neulet.2006.02.017. Epub 2006 Mar 2. Neurosci Lett. 2006. PMID: 16513263

6

A mutation in the GABA(A) receptor alpha(1)-subunit is associated with absence epilepsy.

Maljevic S, Krampfl K, Cobilanschi J, Tilgen N, Beyer S, Weber YG, Schlesinger F, Ursu D, Melzer W, Cossette P, Bufler J, Lerche H, Heils A. Maljevic S, et al. Among authors: lerche h. Ann Neurol. 2006 Jun;59(6):983-7. doi: 10.1002/ana.20874. Ann Neurol. 2006. PMID: 16718694

7

Novel anticonvulsant drugs targeting voltage-dependent ion channels.

Wuttke TV, Lerche H. Wuttke TV, et al. Among authors: lerche h. Expert Opin Investig Drugs. 2006 Oct;15(10):1167-77. doi: 10.1517/13543784.15.10.1167. Expert Opin Investig Drugs. 2006. PMID: 16989594 Review.

8

Exploration of the genetic architecture of idiopathic generalized epilepsies.

Hempelmann A, Taylor KP, Heils A, Lorenz S, Prud'homme JF, Nabbout R, Dulac O, Rudolf G, Zara F, Bianchi A, Robinson R, Gardiner RM, Covanis A, Lindhout D, Stephani U, Elger CE, Weber YG, Lerche H, Nürnberg P, Kron KL, Scheffer IE, Mulley JC, Berkovic SF, Sander T. Hempelmann A, et al. Among authors: lerche h. Epilepsia. 2006 Oct;47(10):1682-90. doi: 10.1111/j.1528-1167.2006.00677.x. Epilepsia. 2006. PMID: 17054691 Free article.

9

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: lerche h. 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

10

Neutralization of a negative charge in the S1-S2 region of the KV7.2 (KCNQ2) channel affects voltage-dependent activation in neonatal epilepsy.

Wuttke TV, Penzien J, Fauler M, Seebohm G, Lehmann-Horn F, Lerche H, Jurkat-Rott K. Wuttke TV, et al. Among authors: lerche h. J Physiol. 2008 Jan 15;586(2):545-55. doi: 10.1113/jphysiol.2007.143826. Epub 2007 Nov 15. J Physiol. 2008. PMID: 18006581 Free PMC article.

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