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Title
Authors
Vol 5, No 2 (2015)
Electromyographic stages of denervation/reinnervation process in neuromuscular diseases: need for revision
Nikitin S.S.
PDF
(Rus)
Vol 6, No 1 (2016)
Miyoshi myopathy: diagnosis of a familial case of dysferlinopathy
Fedotov V.P., Ryzhkova O.P., Polyakov A.V.
PDF
(Rus)
Vol 9, No 4 (2019)
Spinal and bulbar muscular atrophy with pseudomyotonia phenomena: a clinical case report
Nikitin S.S., Grigoryeva V.N., Mashkovich K.A., Mironovich O.L., Ryadninskaya N.V., Polyakov A.V.
PDF
(Rus)
Vol 9, No 4 (2019)
Clinical examination of patients with late-onset Pompe disease: typical and not typical symptoms and signs
Nikitin S.S.
PDF
(Rus)
Vol 5, No 1 (2015)
The hereditary progressive muscular dystrophy type 2A (calpainopathy): a clinical case
Grishina D.A., Suponeva N.A., Shvedkov V.V., Belopasova A.V.
PDF
(Rus)
Vol 9, No 3 (2019)
Infantile and early childhood onset of mitochondrial myopathy due to mutations in the TK2 gene with a phenotype of spinal muscular atrophy 5q: the first cases in Russia
Kurbatov S.A., Tsygankova P.G., Mollaeva K.Y., Bychkov I.O., Itkis Y.S., Zabnenkova V.V., Umakhanova Z.R., Geybatova L.G., Zakharova E.Y.
PDF
(Rus)
Vol 5, No 1 (2015)
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.
PDF
(Rus)
Vol 14, No 3 (2024)
Steroid myopathy in patients with myasthenia gravis: a literature review
Zaytsevskaya S.A., Suponeva N.A., Antonova K.V., Grishina D.A., Narbut A.M.
PDF
(Rus)
Vol 9, No 3 (2019)
Clinical and genetic characteristics of Nonaka myopathy (GNE-myopathy) in russian patients
Dadali E.L., Sharkova I.V., Rudenskaya G.E., Nikitin S.S., Murtazina A.F., Ryzhkova O.P., Chukhrova A.L.
PDF
(Rus)
Vol 5, No 1 (2015)
Acute rhabdomyolysis
de Lonlay P., Mamoune A., Hamel Y., Bahuau M., Vergnaud S., Piraud M., Lallemand L., Nguyen More M., Vio M., Romero N.
PDF
(Rus)
Vol 13, No 1 (2023)
Clinical and genetic characteristics and an algorithm for the differential diagnosis of progressive muscular dystrophies that manifest after a period of normal motor development
Sharkova I.V., Dadali E.L.
PDF
(Rus)
Vol 9, No 3 (2019)
The clinical case of limb-girdle muscle dystrophy 2Q associated with myasthenic syndrome and lung damage
Bardakov S.N., Deev R.V., Mavlikeev M.O., Umakhanova Z.R., Akhmedova P.G., Magomedova R.M., Zulfugarov K.Z., Tsargush V.A., Chekmareva I.A., Yakovlev I.A., Dalgatov G.D., Yakubovsky G.I., Isaev A.A.
PDF
(Rus)
Vol 2, No 3 (2012)
Experience of polymyositis and antisynthetase syndrome treatment with rituximab
Palshina S.G., Nikitin S.S., Vasilyev V.I.
PDF
(Rus)
Vol 12, No 3 (2022)
New classification of limb-girdle muscular dystrophy
Sidorova O.P., Kotov A.S., Bunak M.S., Filyushkin Y.N.
PDF
(Rus)
Vol 9, No 3 (2019)
Mitochondrial disorders in neuromuscular pathology
Kotov S.V., Sidorova O.P., Borodataya E.V.
PDF
(Rus)
Vol 3, No 2 (2013)
The diagnosis and pathogenesis of chronic alcoholic myopathy
Kazantseva Y.V., Zinovyeva O.E., Shenkman B.S., Shcheglova N.S., Lysenko E.A.
PDF
(Rus)
Vol 12, No 2 (2022)
Differential diagnosis of myopathy and multiple epiphysal dysplasia caused by mutations in the COMP gene in children
Markova T.V., Kenis V.M., Nikitin S.S., Melchenko E.V., Nagornova T.S., Osipova D.V., Alieva A.E., Yugeno Y.S., Zakharova E.Y., Dadali E.L.
PDF
(Rus) PDF
(Eng)
Vol 4, No 1 (2014)
Late-onset Pompe disease: first clinical description in Russia
Nikitin S.S., Kovalchuk M.O., Zaharova E.U., Tsivileva V.V.
PDF
(Rus)
Vol 10, No 1 (2020)
Spinal and bulbar muscular atrophy as a multisystem disease with motor neuron and muscle involvement: literature review and a case report
Ivanova E.O., Fedotov E.Y., Illarioshkin S.N.
PDF
(Rus)
Vol 5, No 3 (2015)
Late-onset Pompe disease with phenotype of the limb-girdle muscular dystrophy
Kurbatov S.A., Nikitin S.S., Zakharova E.Y.
PDF
(Rus)
1 - 20 of 20 Items

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