Differential diagnosis of hypokinetic disorders in hereditary neuromuscular diseases | Zendy

Л А Сайкова | Zendy; В Д Косачев | Zendy; В. Г. Пустозеров | Zendy; Т. М. Алексеева | Zendy; Tatyana Vasilyeva | Zendy; I. G. Zavolokov | Zendy

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Differential diagnosis of hypokinetic disorders in hereditary neuromuscular diseases

Author(s) -

Л А Сайкова,

В Д Косачев,

В. Г. Пустозеров,

Т. М. Алексеева,

Tatyana Vasilyeva,

I. G. Zavolokov

Publication year - 1997

Publication title -

neurology bulletin

Language(s) - English

Resource type - Journals

eISSN - 2304-3067

pISSN - 1027-4898

DOI - 10.17816/nb79927

Subject(s) - polymyositis , differential diagnosis , medicine , amyotrophy , physical medicine and rehabilitation , pathology , atrophy

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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