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Clinical and electromyographic criteria for the diagnosis of hereditary myotonic syndromes
Fedotov V.P., Kurbatov S.A., Ivanova E.A., Galeeva N.M., Polyakov A.V.
Clinical case of the late diagnosis of neurolipomatosis (Dercum’s disease)
Shnayder N.A., Kiselev I.A., Dmitrenko D.V.
Adult spinal muscular atrophy: problems of early diagnosis
Shpilyukova Y.A., Illarioshkin S.N.
Lumbosacral motor polyneuropathy
Malmberg S.A., Rudenko E.N.
Differential diagnosis of the disease of the great Russian artist I. Repin
Gorozhanin A.V., Fedyakov A.G., Lovyagina V.E.
Comparative multimodal sensory testing in multifocal motor neuropathy and multifocal variant of chronic inflammatory demyelinating polyradiculoneuropathy
Tumilovich T.A., Grishina D.A., Suponeva N.A., Fedin P.A.
Neurophysiological differential diagnostic markers in hereditary neuropathy with liability to pressure palsies and chronic inflammatory demyelinating polyradiculoneuropathy
Grishina D.A., Suponeva N.A.
Analysis of primary diagnostics of hereditary motor and sensory neuropathies in the Republic of Bashkortostan
Saifullina E.V., Magzhanov R.V., Khidiiatova I.M., Khusnutdinova E.K.
Stiff-person syndrome with early onset in infancy
Malmberg S.A., Dadali E.L., Jumakchanov D.B., Djaksibaeva A.K.
Inherited progressive limb-girdle muscular dystrophy type 2A (calpainopathy): a review of literature
Grishina D.A., Suponeva N.A., Shvedkov V.V., Belopasova A.V.
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