Suchergebnisse - Lehmann–Horn, Frank

Muscle channelopathies and critical points in functional and genetic studies von Jurkat-Rott, Karin, Lehmann-Horn, Frank

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The impact of splice isoforms on voltage-gated calcium channel α(1) subunits von Jurkat-Rott, Karin, Lehmann-Horn, Frank

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Do Hyperpolarization-induced Proton Currents Contribute to the Pathogenesis of Hypokalemic Periodic Paralysis, a Voltage Sensor Channelopathy? von Jurkat-Rott, Karin, Lehmann-Horn, Frank

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Pathophysiological Role of Omega Pore Current in Channelopathies von Jurkat-Rott, Karin, Groome, James, Lehmann-Horn, Frank

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Eplerenone repolarizes muscle membrane through Na,K-ATPase activation by Tyr10 dephosphorylation von Breitenbach, Simon, Lehmann-Horn, Frank, Jurkat-Rott, Karin

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Letter to the Editor concerning “A hypothesis of chronic back pain: ligament subfailure injuries lead to muscle control dysfunction” (M. Panjabi) von Schleip, Robert, Vleeming, Andry, Lehmann-Horn, Frank, Klingler, Werner

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Open- and closed-state fast inactivation in sodium channels: Differential effects of a site-3 anemone toxin von Groome, James R, Lehmann-Horn, Frank, Holzherr, Boris D

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The impact of permanent muscle weakness on quality of life in periodic paralysis: a survey of 66 patients von CAVEL-GREANT, DEBORAH, LEHMANN-HORN, FRANK, JURKAT-ROTT, KARIN

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Domain III S4 in closed-state fast inactivation: Insights from a periodic paralysis mutation von Groome, James R, Jurkat-Rott, Karin, Lehmann-Horn, Frank

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Sodium channelopathies of skeletal muscle result from gain or loss of function von Jurkat-Rott, Karin, Holzherr, Boris, Fauler, Michael, Lehmann-Horn, Frank

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The role of fibrosis in Duchenne muscular dystrophy von KLINGLER, WERNER, JURKAT-ROTT, KARIN, LEHMANN-HORN, FRANK, SCHLEIP, ROBERT

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Successful treatment of periodic paralysis with coenzyme Q10: two case reports von Da, Yuwei, Lei, Lin, Jurkat-Rott, Karin, Lehmann-Horn, Frank

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Mechanisms of cold sensitivity of paramyotonia congenita mutation R1448H and overlap syndrome mutation M1360V von Mohammadi, Bahram, Mitrovic, Nenad, Lehmann-Horn, Frank, Dengler, Reinhard, Bufler, Johannes

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A gating model for wildtype and R1448H Nav1.4 channels in paramyotonia von HOLZHERR, BORIS, LEHMANN-HORN, FRANK, KUZMENKINA, ELZA, FAN, CHUNXIANG, JURKAT-ROTT, KARIN

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Cooperative effect of S4–S5 loops in domains D3 and D4 on fast inactivation of the Na(+) channel von Oana Popa, M, Alekov, Alexi K, Bail, Sigrid, Lehmann-Horn, Frank, Lerche, Holger

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A sodium channel mutation causing epilepsy in man exhibits subtle defects in fast inactivation and activation in vitro von Alekov, Alexi K, Rahman, Md Masmudur, Mitrovic, Nenad, Lehmann-Horn, Frank, Lerche, Holger

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Elevation of extracellular osmolarity improves signs of myotonia congenita in vitro: a preclinical animal study von Hoppe, Kerstin, Chaiklieng, Sunisa, Lehmann‐Horn, Frank, Jurkat‐Rott, Karin, Wearing, Scott, Klingler, Werner

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Na(V)1.4 DI-S4 periodic paralysis mutation R222W enhances inactivation and promotes leak current to attenuate action potentials and depolarize muscle fibers von Bayless-Edwards, Landon, Winston, Vern, Lehmann-Horn, Frank, Arinze, Paula, Groome, James R., Jurkat-Rott, Karin

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Neutralization of a negative charge in the S1–S2 region of the K(V)7.2 (KCNQ2) channel affects voltage-dependent activation in neonatal epilepsy von Wuttke, Thomas V, Penzien, Johann, Fauler, Michael, Seebohm, Guiscard, Lehmann-Horn, Frank, Lerche, Holger, Jurkat-Rott, Karin

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Na(V)1.4 mutations cause hypokalaemic periodic paralysis by disrupting IIIS4 movement during recovery von Groome, James R., Lehmann-Horn, Frank, Fan, Chunxiang, Wolf, Markus, Winston, Vern, Merlini, Luciano, Jurkat-Rott, Karin

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