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Hereditary Channelopathies in Neurology
Jurkat-Rott, Karin et al. (2010)
Teil eines Buches
Comparative analysis of brain structure, metabolism, and cognition in myotonic dystrophy 1 and 2
Weber, Y. G. et al. (2010)
Wissenschaftlicher Artikel
Sodium channelopathies of skeletal muscle result from gain or loss of function
Jurkat-Rott, Karin et al. (2010)
Wissenschaftlicher Artikel
Recovery of mechano-electrical transduction in rat cochlear hair bundles after postnatal destruction of the stereociliar cross-links
Ebert, J. et al. (2010)
Wissenschaftlicher Artikel
Principles of Electrophysiological In Vitro Measurements
Lehmann-Horn, Frank et al. (2010)
Teil eines Buches
Biomechanical Properties of Fascial Tissues and Their Role as Pain Generators
Schleip, Robert; Zorn, Adjo; Klingler, Werner (2010)
Wissenschaftlicher Artikel
SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain
Liao, Y. et al. (2010)
Wissenschaftlicher Artikel
S100A1 promotes action potential-initiated calcium release flux and force production in skeletal muscle
Prosser, Benjamin L. et al. (2010)
Wissenschaftlicher Artikel
Genetic testing in the epilepsies-Report of the ILAE Genetics Commission
Ottman, Ruth et al. (2010)
Wissenschaftlicher Artikel
Axon initial segment dysfunction in a mouse model of genetic epilepsy with febrile seizures plus
Wimmer, Verena C. et al. (2010)
Wissenschaftlicher Artikel