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PRRT2 Mutations Are the Major Cause of Benign Familial Infantile Seizures
Schubert, Julian et al. (2012)
Wissenschaftlicher Artikel
Acetazolamide-responsive exercise-induced episodic ataxia associated with a novel homozygous DARS2 mutation
Synofzik, Matthis et al. (2011)
Wissenschaftlicher Artikel
Altered stress stimulation of inward rectifier potassium channels in Andersen-Tawil syndrome
Seebohm, Guiscard et al. (2012)
Wissenschaftlicher Artikel
Disease-causing mutations C277R and C277Y modify gating of human ClC-1 chloride channels in myotonia congenita
Weinberger, Sebastian et al. (2012)
Wissenschaftlicher Artikel
Monogenic channelopathies of the skeletal muscle
Lehmann-Horn, Frank; Jurkat-Rott, K. (2013)
Wissenschaftlicher Artikel
7-T Cl-35 and Na-23 MR Imaging for Detection of Mutation-dependent Alterations in Muscular Edema and Fat Fraction with Sodium and Chloride Concentrations in Muscular Periodic Paralyses
Weber, Marc-Andre et al. (2016)
Wissenschaftlicher Artikel
Pathophysiological role of omega pore current in channelopathies
Jurkat-Rott, Karin; Groome, James; Lehmann-Horn, Frank (2012)
Wissenschaftlicher Artikel
Open-and closed-state fast inactivation in sodium channels Differential effects of a site-3 anemone toxin
Groome, James R.; Lehmann-Horn, Frank; Holzherr, Boris D. (2011)
Wissenschaftlicher Artikel
In vitro muscle contracture investigations on the malignant hyperthermia like episodes in myotonia congenita
Hoppe, K. et al. (2013)
Wissenschaftlicher Artikel
Muscle channelopathies. Myotonias and periodic paralyses
Jurkat-Rott, K.; Lerche, H.; Lehmann-Horn, Frank (2011)
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