Differential diagnosis of hypokinetic disorders in hereditary neuromuscular diseases
- Authors: Saikova L.A.1, Kosachev V.D.1, Pustozerov V.G.1, Alekseeva Т.M.1, Vasilyeva Т.N.1, Zavolokov I.G.1
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Affiliations:
- Medical Academy of Postgraduate Education
- Issue: Vol XXIX, No 1-2 (1997)
- Pages: 81-83
- Section: Articles
- URL: https://bakhtiniada.ru/1027-4898/article/view/79927
- DOI: https://doi.org/10.17816/nb79927
- ID: 79927
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Abstract
For determination criteria of differential diagnosis analysis of clinical manifestations and indices of additional research methods (EMG, ENMY, biochemical, histomorphological) of paroxysmal hypokinetic conditions in myoplegia, myopathic syndromes, glycogenosis and Mc Ardl syndrome in polymyositis, Eulenburg-Lewandowsky paramyotoxia, remittent form of neural amyotrophy, some forms of congenital myopathies was carried out.
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##article.viewOnOriginalSite##About the authors
L. A. Saikova
Medical Academy of Postgraduate Education
Author for correspondence.
Email: info@eco-vector.com
Russian Federation, Saint Petersburg
V. D. Kosachev
Medical Academy of Postgraduate Education
Email: info@eco-vector.com
Russian Federation, Saint Petersburg
V. G. Pustozerov
Medical Academy of Postgraduate Education
Email: info@eco-vector.com
Russian Federation, Saint Petersburg
Т. M. Alekseeva
Medical Academy of Postgraduate Education
Email: info@eco-vector.com
Russian Federation, Saint Petersburg
Т. N. Vasilyeva
Medical Academy of Postgraduate Education
Email: info@eco-vector.com
Russian Federation, Saint Petersburg
I. G. Zavolokov
Medical Academy of Postgraduate Education
Email: info@eco-vector.com
Russian Federation, Saint Petersburg
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