Lerche H - Search Results

1

Mutations in GABRB3: From febrile seizures to epileptic encephalopathies.

Møller RS, Wuttke TV, Helbig I, Marini C, Johannesen KM, Brilstra EH, Vaher U, Borggraefe I, Talvik I, Talvik T, Kluger G, Francois LL, Lesca G, de Bellescize J, Blichfeldt S, Chatron N, Holert N, Jacobs J, Swinkels M, Betzler C, Syrbe S, Nikanorova M, Myers CT, Larsen LH, Vejzovic S, Pendziwiat M, von Spiczak S, Hopkins S, Dubbs H, Mang Y, Mukhin K, Holthausen H, van Gassen KL, Dahl HA, Tommerup N, Mefford HC, Rubboli G, Guerrini R, Lemke JR, Lerche H, Muhle H, Maljevic S. Møller RS, et al. Among authors: lerche h. Neurology. 2017 Jan 31;88(5):483-492. doi: 10.1212/WNL.0000000000003565. Epub 2017 Jan 4. Neurology. 2017. PMID: 28053010 Free PMC article.

2

Enhanced inactivation and pH sensitivity of Na(+) channel mutations causing hypokalaemic periodic paralysis type II.

Kuzmenkin A, Muncan V, Jurkat-Rott K, Hang C, Lerche H, Lehmann-Horn F, Mitrovic N. Kuzmenkin A, et al. Among authors: lerche h. Brain. 2002 Apr;125(Pt 4):835-43. doi: 10.1093/brain/awf071. Brain. 2002. PMID: 11912116

3

Skeletal muscle channelopathies.

Jurkat-Rott K, Lerche H, Lehmann-Horn F. Jurkat-Rott K, et al. Among authors: lerche h. J Neurol. 2002 Nov;249(11):1493-502. doi: 10.1007/s00415-002-0871-5. J Neurol. 2002. PMID: 12420087 Review.

4

C-terminal interaction of KCNQ2 and KCNQ3 K+ channels.

Maljevic S, Lerche C, Seebohm G, Alekov AK, Busch AE, Lerche H. Maljevic S, et al. Among authors: lerche c, lerche h. J Physiol. 2003 Apr 15;548(Pt 2):353-60. doi: 10.1113/jphysiol.2003.040980. Epub 2003 Mar 14. J Physiol. 2003. PMID: 12640002 Free PMC article.

5

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

6

Molecular analysis of the A322D mutation in the GABA receptor alpha-subunit causing juvenile myoclonic epilepsy.

Krampfl K, Maljevic S, Cossette P, Ziegler E, Rouleau GA, Lerche H, Bufler J. Krampfl K, et al. Among authors: lerche h. Eur J Neurosci. 2005 Jul;22(1):10-20. doi: 10.1111/j.1460-9568.2005.04168.x. Eur J Neurosci. 2005. PMID: 16029191

7

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.

8

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

9

Subthreshold changes of voltage-dependent activation of the K(V)7.2 channel in neonatal epilepsy.

Hunter J, Maljevic S, Shankar A, Siegel A, Weissman B, Holt P, Olson L, Lerche H, Escayg A. Hunter J, et al. Among authors: lerche h. Neurobiol Dis. 2006 Oct;24(1):194-201. doi: 10.1016/j.nbd.2006.06.011. Epub 2006 Aug 17. Neurobiol Dis. 2006. PMID: 16916607

10

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.

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