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Myotonia: A review of biochemical studies Shiro MAWATARI 1,2 1Department of Neurology, College of Physicians and Surgeons, Columbia University 2Department of Neurology, Neurological Institute, Faculty of Medicine, Kyushu University pp.20-25
Published Date 1976/2/10
DOI https://doi.org/10.11477/mf.1431903811
  • Abstract
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Myotonia is a characteristic phenomenon or symptom of myotonic dystrophy, myotonia congenita and paramyotonia in man, and of a hereditary disease of goats. This phenomenon can be induced by a number of chemical compounds including hypocholesterolemic drugs and monocarboxylic aromatic acids. The site of the defect in myotonia has been considered to be muscle cell itself since the myotonia persists despite denervation or curalization of the muscle, although some studies have suggested that the muscle changes are secondary to a primary defect of the nervous system.


Copyright © 1976, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1243 印刷版ISSN 0001-8724 医学書院

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