Differential diagnosis of hypokinetic disorders in hereditary neuromuscular diseases
L. A. Saikova , V. D. Kosachev , V. G. Pustozerov , Т. M. Alekseeva , Т. N. Vasilyeva , I. G. Zavolokov
Neurology Bulletin ›› 1997, Vol. XXIX ›› Issue (1-2) : 81 -83.
Differential diagnosis of hypokinetic disorders in hereditary neuromuscular diseases
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.
Neurological archive of Bekhterev
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Saikova L.A., Kosachev V.D., Pustozerov V.G., Alekseeva Т.M., Vasilyeva Т.N., Zavolokov I.G.
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