Full text
PDF
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Almers W., Stanfield P. R., Stühmer W. Slow changes in currents through sodium channels in frog muscle membrane. J Physiol. 1983 Jun;339:253–271. doi: 10.1113/jphysiol.1983.sp014715. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cannon S. C., Brown R. H., Jr, Corey D. P. A sodium channel defect in hyperkalemic periodic paralysis: potassium-induced failure of inactivation. Neuron. 1991 Apr;6(4):619–626. doi: 10.1016/0896-6273(91)90064-7. [DOI] [PubMed] [Google Scholar]
- Cannon S. C., Brown R. H., Jr, Corey D. P. Theoretical reconstruction of myotonia and paralysis caused by incomplete inactivation of sodium channels. Biophys J. 1993 Jul;65(1):270–288. doi: 10.1016/S0006-3495(93)81045-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cannon S. C., Corey D. P. Loss of Na+ channel inactivation by anemone toxin (ATX II) mimics the myotonic state in hyperkalaemic periodic paralysis. J Physiol. 1993 Jul;466:501–520. [PMC free article] [PubMed] [Google Scholar]
- Lerche H., Heine R., Pika U., George A. L., Jr, Mitrovic N., Browatzki M., Weiss T., Rivet-Bastide M., Franke C., Lomonaco M. Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III-IV linker. J Physiol. 1993 Oct;470:13–22. doi: 10.1113/jphysiol.1993.sp019843. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ptacek L. J., Johnson K. J., Griggs R. C. Genetics and physiology of the myotonic muscle disorders. N Engl J Med. 1993 Feb 18;328(7):482–489. doi: 10.1056/NEJM199302183280707. [DOI] [PubMed] [Google Scholar]
- Ruff R. L., Simoncini L., Stühmer W. Slow sodium channel inactivation in mammalian muscle: a possible role in regulating excitability. Muscle Nerve. 1988 May;11(5):502–510. doi: 10.1002/mus.880110514. [DOI] [PubMed] [Google Scholar]