Characterization of hyperkalemic periodic paralysis: a survey of genetically diagnosed individuals by Charles, G., Zheng, C., Lehmann-Horn, F., Jurkat-Rott, K., Levitt, J.

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Effects of S906T polymorphism on the severity of a novel borderline mutation I692M in Nav1.4 cause periodic paralysis by Fan, C., Mao, N., Lehmann‐Horn, F., Bürmann, J., Jurkat‐Rott, K.

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Contractile elements in muscular fascial tissue – implications for in‐vitro contracture testing for malignant hyperthermia by Hoppe, K., Schleip, R., Lehmann‐Horn, F., Jäger, H., Klingler, W.

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In vitro muscle contracture investigations on the malignant hyperthermia like episodes in myotonia congenita by HOPPE, K., LEHMANN-HORN, F., CHAIKLIENG, S., JURKAT-ROTT, K., ADOLPH, O., KLINGLER, W.

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Recovery of mechano-electrical transduction in rat cochlear hair bundles after postnatal destruction of the stereociliar cross-links by Ebert, J., Fink, S., Koitschev, A., Walther, P., Langer, M. G., Lehmann-Horn, F.

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A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions by Lerche, H., Biervert, C., Alekov, A. K., Schleithoff, L., Lindner, M., Klingler, W., Bretschneider, F., Mitrovic, N., Jurkat-Rott, K., Bode, H., Lehmann-Horn, F., Steinlein, O. K.

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A possible role of the junctional face protein JP-45 in modulating Ca2+ release in skeletal muscle by Gouadon, E, Schuhmeier, R P, Ursu, D, Anderson, A A, Treves, S, Zorzato, F, Lehmann-Horn, F, Melzer, W

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Effects of S906T polymorphism on the severity of a novel borderline mutation I692M in Na v 1.4 cause periodic paralysis by Fan, C, Mao, N, Lehmann-Horn, F, Bürmann, J, Jurkat-Rott, K

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Permanent muscular sodium overload and persistent muscle edema in Duchenne muscular dystrophy: a possible contributor of progressive muscle degeneration by Weber, M.-A., Nagel, A. M., Wolf, M. B., Jurkat-Rott, K., Kauczor, H.-U., Semmler, W., Lehmann-Horn, F.

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Active fascial contractility: Fascia may be able to contract in a smooth muscle-like manner and thereby influence musculoskeletal dynamics by Schleip, R., Klingler, W., Lehmann-Horn, F.

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In vitro contracture test for diagnosis of malignant hyperthermia following the protocol of the European MH Group: Results of testing patients surviving fulminant MH and unrelated... by ØRDING, H., BRANCADORO, V., COZZOLINO, S., ELLIS, F. R., GLAUBER, V., GONANO, E. F., HALSALL, P. J., HARTUNG, E., HEFFRON, J. J. A., HEYTENS, L., KOZAK-RIBBENS, G., KRESS, H., KRTVOSIC-HORBER, R., LEHMANN-HORN, F., MORTIER, W., NIVOCHE, Y., RANKLEV-TWETMAN, E., SIGURDSSON, S., SNOECK, M., STIEGLITZ, P., TEGAZZIN, V., URWYLER, A., WAPPLER, F.

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ICCN2010-NL1 Myotonias as channelopathies by Lehmann-Horn, F

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Mechanisms of cold sensitivity of paramyotonia congenita mutation R1448H and overlap syndrome mutation M1360V by Mohammadi, B., Mitrovic, N., Lehmann-Horn, F., Dengler, R., Bufler, J.

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Role in fast inactivation of the IV/S4-S5 loop of the human muscle Na+ channel probed by cysteine mutagenesis by Lerche, H., Peter, W., Fleischhauer, R., Pika‐Hartlaub, U., Malina, T., Mitrovic, N., Lehmann‐Horn, F.

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Different effects on gating of three myotonia-causing mutations in the inactivation gate of the human muscle sodium channel by N MitroviÄ, A L George, Jr, H Lerche, S Wagner, C Fahlke, F Lehmann-Horn

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Malignant hyperthermia mutation Arg615Cys in the porcine ryanodine receptor alters voltage dependence of Ca2+ release by Dietze, B., Henke, J., Eichinger, H. M., Lehmann‐Horn, F., Melzer, W.

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S44-5 Chloride and sodium channel myotonias by Lehmann-Horn, F, Deymeer, F, Jurkat-Rott, K

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S45-4 Periodic paralysis by Jurkat-Rott, K, Lehmann-Horn, F

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K(+)-aggravated myotonia: destabilization of the inactivated state of the human muscle Na+ channel by the V1589M mutation by N MitroviÄ, A L George, Jr, R Heine, S Wagner, U Pika, U Hartlaub, M Zhou, H Lerche, C Fahlke, F Lehmann-Horn

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135. Electrophysiological decrement and transient weakness in myotonic syndromes by Matur, Z, Ciftci, F.D, Kara, B, Serdaroglu-Oflazer, P, Parman, Y, Basak, N, Jurkat-Rott, K, Lehmann-Horn, F, Deymeer, F

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