Lehmann-Horn F - Search Results

1

Mechanisms of cold sensitivity of paramyotonia congenita mutation R1448H and overlap syndrome mutation M1360V.

Mohammadi B, Mitrovic N, Lehmann-Horn F, Dengler R, Bufler J. Mohammadi B, et al. J Physiol. 2003 Mar 15;547(Pt 3):691-8. doi: 10.1113/jphysiol.2002.033928. Epub 2003 Jan 24. J Physiol. 2003. PMID: 12562902 Free PMC article.

2

Preferred mexiletine block of human sodium channels with IVS4 mutations and its pH-dependence.

Mohammadi B, Jurkat-Rott K, Alekov A, Dengler R, Bufler J, Lehmann-Horn F. Mohammadi B, et al. Pharmacogenet Genomics. 2005 Apr;15(4):235-44. doi: 10.1097/01213011-200504000-00007. Pharmacogenet Genomics. 2005. PMID: 15864116

3

Effects of temperature and mexiletine on the F1473S Na+ channel mutation causing paramyotonia congenita.

Fleischhauer R, Mitrovic N, Deymeer F, Lehmann-Horn F, Lerche H. Fleischhauer R, et al. Pflugers Arch. 1998 Oct;436(5):757-65. doi: 10.1007/s004240050699. Pflugers Arch. 1998. PMID: 9716710

4

A human muscle Na+ channel mutation in the voltage sensor IV/S4 affects channel block by the pentapeptide KIFMK.

Peter W, Mitrovic N, Schiebe M, Lehmann-Horn F, Lerche H. Peter W, et al. J Physiol. 1999 Jul 1;518(Pt 1):13-22. doi: 10.1111/j.1469-7793.1999.0013r.x. J Physiol. 1999. PMID: 10373685 Free PMC article.

5

Different effects of mexiletine on two mutant sodium channels causing paramyotonia congenita and hyperkalemic periodic paralysis.

Weckbecker K, Würz A, Mohammadi B, Mansuroglu T, George AL Jr, Lerche H, Dengler R, Lehmann-Horn F, Mitrovic N. Weckbecker K, et al. Neuromuscul Disord. 2000 Jan;10(1):31-9. doi: 10.1016/s0960-8966(99)00060-7. Neuromuscul Disord. 2000. PMID: 10677861

6

A sodium channel mutation causing epilepsy in man exhibits subtle defects in fast inactivation and activation in vitro.

Alekov A, Rahman MM, Mitrovic N, Lehmann-Horn F, Lerche H. Alekov A, et al. J Physiol. 2000 Dec 15;529 Pt 3(Pt 3):533-9. doi: 10.1111/j.1469-7793.2000.00533.x. J Physiol. 2000. PMID: 11118488 Free PMC article.

7

Impaired slow inactivation due to a polymorphism and substitutions of Ser-906 in the II-III loop of the human Nav1.4 channel.

Kuzmenkin A, Jurkat-Rott K, Lehmann-Horn F, Mitrovic N. Kuzmenkin A, et al. Pflugers Arch. 2003 Oct;447(1):71-7. doi: 10.1007/s00424-003-1137-5. Epub 2003 Jul 26. Pflugers Arch. 2003. PMID: 12898257

8

K(+)-aggravated myotonia: destabilization of the inactivated state of the human muscle Na+ channel by the V1589M mutation.

Mitrović N, George AL Jr, Heine R, Wagner S, Pika U, Hartlaub U, Zhou M, Lerche H, Fahlke C, Lehmann-Horn F. Mitrović N, et al. J Physiol. 1994 Aug 1;478 Pt 3(Pt 3):395-402. doi: 10.1113/jphysiol.1994.sp020260. J Physiol. 1994. PMID: 7965854 Free PMC article.

9

Paramyotonia congenita: the R1448P Na+ channel mutation in adult human skeletal muscle.

Lerche H, Mitrovic N, Dubowitz V, Lehmann-Horn F. Lerche H, et al. Ann Neurol. 1996 May;39(5):599-608. doi: 10.1002/ana.410390509. Ann Neurol. 1996. PMID: 8619545

10

Role in fast inactivation of the IV/S4-S5 loop of the human muscle Na+ channel probed by cysteine mutagenesis.

Lerche H, Peter W, Fleischhauer R, Pika-Hartlaub U, Malina T, Mitrovic N, Lehmann-Horn F. Lerche H, et al. J Physiol. 1997 Dec 1;505 ( Pt 2)(Pt 2):345-52. doi: 10.1111/j.1469-7793.1997.345bb.x. J Physiol. 1997. PMID: 9423178 Free PMC article.

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