Altered sodium channel behaviour causes myotonia in dominantly inherited myotonia congenita
- 31 December 1991
- journal article
- Published by Elsevier in Neuromuscular Disorders
- Vol. 1 (1) , 47-53
- https://doi.org/10.1016/0960-8966(91)90042-q
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Schwartz–Jampel syndrome: II. Na+ channel defect causes myotoniaMuscle & Nerve, 1990
- Myotonia FluctuansArchives of Neurology, 1990
- Characteristics of single Na+ channels of adult human skeletal musclePflügers Archiv - European Journal of Physiology, 1990
- Transient weakness and altered membrane characteristic in recessive generalized myotonia (Becker)Muscle & Nerve, 1988
- Membrane defects in paramyotonia congenita (eulenburg)Muscle & Nerve, 1987
- Adynamia episodica hereditaria with myotonia: A non‐inactivating sodium current and the effect of extracellular pHMuscle & Nerve, 1987
- Membrane changes in cells from myotonia patients.Physiological Reviews, 1985
- Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patchesPflügers Archiv - European Journal of Physiology, 1981
- MyotoniaArchives of Neurology, 1975
- Tonische Krämpfe in willkürlich beweglichen Muskeln in Folge von ererbter psychischer DispositionArchiv Fur Psychiatrie Und Nervenkrankheiten, 1876