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PRRT2 Mutations Are the Major Cause of Benign Familial Infantile Seizures
Schubert, Julian et al. (2012)
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Altered stress stimulation of inward rectifier potassium channels in Andersen-Tawil syndrome
Seebohm, Guiscard et al. (2012)
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Disease-causing mutations C277R and C277Y modify gating of human ClC-1 chloride channels in myotonia congenita
Weinberger, Sebastian et al. (2012)
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Pathophysiological role of omega pore current in channelopathies
Jurkat-Rott, Karin; Groome, James; Lehmann-Horn, Frank (2012)
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Evaluation of Myoplasmic Sodium in Hyperkalemic Periodic Paralysis with 3Tesla Magnetic Resonance Imaging
Amarteifio, E. et al. (2012)
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Hyperkalemic Periodic Paralysis and Permanent Weakness: 3-T MR Imaging Depicts Intracellular Na-23 Overload-Initial Results
Amarteifio, Erick et al. (2012)
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Membrane excitability and excitation-contraction uncoupling in muscle fatigue
Fouler, Michael; Jurkat-Rott, Karin; Lehmann-Horn, Frank (2012)
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Permanent muscular sodium overload and persistent muscle edema in Duchenne muscular dystrophy: a possible contributor of progressive muscle degeneration
Weber, M. -A. et al. (2012)
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A Becker myotonia patient with compound heterozygosity for CLCN1 mutations and Prinzmetal angina pectoris
Zielonka, Daniel et al. (2012)
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