The familial periodic paralyses and nondystrophic myotonias
- 1 July 1998
- journal article
- review article
- Published by Elsevier in The American Journal of Medicine
- Vol. 105 (1) , 58-70
- https://doi.org/10.1016/s0002-9343(98)00123-5
Abstract
No abstract availableThis publication has 66 references indexed in Scilit:
- Channelopathies: ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous systemNeuromuscular Disorders, 1997
- Sodium channel mutations in acetazolamide‐responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysisNeurology, 1994
- A novel SCN4A mutation causing myotonia aggravated by cold and potassiumHuman Molecular Genetics, 1993
- Genetics and Physiology of the Myotonic Muscle DisordersNew England Journal of Medicine, 1993
- The Periodic ParalysesHospital Practice, 1992
- Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenitaNeuron, 1992
- Temperature-sensitive mutations in the III–IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenitaCell, 1992
- A Met-to-Val mutation in the skeletal muscle Na+ channel α-subunit in hyperkalaemic periodic paralysisNature, 1991
- Identification of a mutation in the gene causing hyperkalemic periodic paralysisCell, 1991
- STUDIES IN DISORDERS OF MUSCLE. VII. CLINICAL MANIFESTATIONS AND INHERITANCE OF A TYPE OF PERIODIC PARALYSIS WITHOUT HYPOPOTASSEMIA 1Journal of Clinical Investigation, 1951