Showing results (21-30 of 34) with videos related to
Sort By:
Pageof 4
Zhurnal Nevropatologii I Psikhiatrii Imeni S.S. Korsakova (Moscow, Russia : 1952)|January 1, 1987
[Clinico-electrophysiological analysis of mitochondrial myopathy]B M Gekht, L L Babakova, L F Kasatkina, et al.Zhurnal Nevropatologii I Psikhiatrii Imeni S.S. Korsakova (Moscow, Russia : 1952)|January 1, 1985
[Strategy for using glucocorticoid preparations in neuromuscular diseases]B M Gekht, E A Kolomenskaia, D I Shagal, et al.Zhurnal Nevropatologii I Psikhiatrii Imeni S.S. Korsakova (Moscow, Russia : 1952)|January 1, 1979
[Pathogenetic therapy of nervous system and muscular diseases using large doses of prednisolone on alternate days]B M Gekht, M I Kuzin, E A Kolomenskaia, et al.Zhurnal Nevropatologii I Psikhiatrii Imeni S.S. Korsakova (Moscow, Russia : 1952)|January 1, 1981
[Electromyographic and morphological analysis of the changes in the motor units in myasthenia, combined myasthenia with thymoma and polymyositis and terminal polyneuropathy with myasthenic syndrome]B M Gekht, V V Gustaĭnis, L F Kasatkina, et al.Neuroscience and Behavioral Physiology|July 1, 1984
Clinical and electromyographic characteristics of pathological muscular-fatigue syndromes of the myasthenia typeL B Perel'man, E G Almazova, L F Kasatkina, et al.Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|July 23, 2003
[Photopheresis--anew method for treatment of myasthenia]V Ia Neretin, A V Kil'diushevskiĭ, B V Agafonov, et al.Klinicheskaia Meditsina|November 8, 2006
[The differential diagnostic criteria and clinical features of endocrine ophtalmopathy in patients suffering from myastenia with oculomotor disturbances]V N Zakutniaia, A S Ametov, B M Gekht, et al.Vestnik Rossiiskoi Akademii Meditsinskikh Nauk|January 1, 1995
[Analysis of the association of ABO blood groups and Rhesus factor with myasthenia]B M Gekht, B V Agafonov, V G Tsuman, et al.Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|August 29, 2001
[Antigens of histocompatibility in children with myasthenia gravis]V Ia Neretin, L D Serova, B V Agafonov, et al.Neuropediatrics|January 22, 2003
Congenital myasthenic syndrome (CMS) in three European kinships due to a novel splice mutation (IVS7 - 2 A/G) in the epsilon acetylcholine receptor (AChR) subunit geneN Barisic, C Schmidt, O P Sidorova, et al.Pageof 4