Lerche H - Search Results

1

Novel KCNQ3 Mutation in a Large Family with Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal Seizures.

Maljevic S, Vejzovic S, Bernhard MK, Bertsche A, Weise S, Döcker M, Lerche H, Lemke JR, Merkenschlager A, Syrbe S. Maljevic S, et al. Among authors: lerche h. Mol Syndromol. 2016 Sep;7(4):189-196. doi: 10.1159/000447461. Epub 2016 Jul 7. Mol Syndromol. 2016. PMID: 27781029 Free PMC article.

2

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.

3

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

4

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

5

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

6

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

7

Nervous system KV7 disorders: breakdown of a subthreshold brake.

Maljevic S, Wuttke TV, Lerche H. Maljevic S, et al. Among authors: lerche h. J Physiol. 2008 Apr 1;586(7):1791-801. doi: 10.1113/jphysiol.2008.150656. Epub 2008 Jan 31. J Physiol. 2008. PMID: 18238816 Free PMC article. Review.

8

Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsy.

Liao Y, Deprez L, Maljevic S, Pitsch J, Claes L, Hristova D, Jordanova A, Ala-Mello S, Bellan-Koch A, Blazevic D, Schubert S, Thomas EA, Petrou S, Becker AJ, De Jonghe P, Lerche H. Liao Y, et al. Among authors: lerche h. Brain. 2010 May;133(Pt 5):1403-14. doi: 10.1093/brain/awq057. Epub 2010 Apr 5. Brain. 2010. PMID: 20371507

9

KV7 channelopathies.

Maljevic S, Wuttke TV, Seebohm G, Lerche H. Maljevic S, et al. Among authors: lerche h. Pflugers Arch. 2010 Jul;460(2):277-88. doi: 10.1007/s00424-010-0831-3. Epub 2010 Apr 18. Pflugers Arch. 2010. PMID: 20401729 Review.

10

Temperature and pharmacological rescue of a folding-defective, dominant-negative KV 7.2 mutation associated with neonatal seizures.

Maljevic S, Naros G, Yalçin Ö, Blazevic D, Loeffler H, Cağlayan H, Steinlein OK, Lerche H. Maljevic S, et al. Among authors: lerche h. Hum Mutat. 2011 Oct;32(10):E2283-93. doi: 10.1002/humu.21554. Hum Mutat. 2011. PMID: 21913284

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