Muscle channelopathies: does the predicted channel gating pore offer new treatment insights for hypokalaemic periodic paralysis?

Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family

(2009) Tie Ke et al.   JOURNAL OF HUMAN GENETICS

Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis

(2009) E. Matthews et al.   NEUROLOGY

K+-dependent paradoxical membrane depolarization and Na+ overload, major and reversible contributors to weakness by ion channel leaks

(2009) K. Jurkat-Rott et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Acetazolamide prevents vacuolar myopathy in skeletal muscle of K+-depleted rats

(2008) D Tricarico et al.   BRITISH JOURNAL OF PHARMACOLOGY

Gating Pore Currents in DIIS4 Mutations of NaV1.4 Associated with Periodic Paralysis: Saturation of Ion Flux and Implications for Disease Pathogenesis

(2008) Arie F. Struyk et al.   JOURNAL OF GENERAL PHYSIOLOGY

Depolarization-activated gating pore current conducted by mutant sodium channels in potassium-sensitive normokalemic periodic paralysis

(2008) S. Sokolov et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Carbonic anhydrases IV and IX: subcellular localization and functional role in mouse skeletal muscle

(2007) Renate J. Scheibe et al.   AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY

Paradoxical depolarization of BA2+- treated muscle exposed to low extracellular K+: Insights into resting potential abnormalities in hypokalemic paralysis

(2007) Arie F. Struyk et al.   MUSCLE & NERVE