Spinal Muscular Atrophy 5q under the Mask of Myopathy: 10 Clinical Cases

by Sergei A. Kurbatov
Published 2021-12-01

Late-onset Pompe disease with phenotype of the limb-girdle muscular dystrophy

by S. A. Kurbatov, S. S. Nikitin, E. Yu. Zakharova
Published 2015-09-01

Spectrum of sonographic changes in hereditary motor and sensory neuropathy with autosomal dominant and X-linked inheritance

by E. S. Naumova, D. S. Druzhinin, S. S. Nikitin, S. A. Kurbatov
Published 2016-07-01

Development of the thermostrengthening regimes of reinforcing steel No 25-36 in conditions of mill 320 of the Belurussian metallurgical works

by V. I. Shcherbakov, G. A. Kurbatov, V. A. Tishchenko
Published 2002-05-01

A case of Becker myotonia with pseudodominant inheritance: сurrent approaches to the differential diagnosis of Thomsen’s and Becker's myotonia congenita

by S. A. Kurbatov, S. S. Nikitin, S. N. Illarioshkin, P. Gundorova, A. V. Polyakov
Published 2016-03-01

Electrodeposition of Mo/MoOx on Copper Substrate from Dimethyl Sulfoxide Solutions

by A. Dauletbay, W. Braida, M. Nauryzbaev, L. Kudreeva, A. Kurbatov, A. Tulegenov
Published 2011-12-01

Differential diagnosis of mitochondrial neurogastrointestinal encephalomyopathy. First clinical description in Russia

by S. A. Kurbatov, V. P. Fedotov, P. G. Tsygankova, E. Y. Zakharova, S. N. Lipovka
Published 2015-06-01

A familial case of segregation of motor sensory neuropathy type 1B with multiple exostoses in monozygous twins

by V. P. Fedotov, S. A. Kurbatov, S. S. Nikitin, T. B. Milovidova, N. M. Galeeva, A. V. Polyakov
Published 2015-05-01

Clinical and electromyographic criteria for the diagnosis of hereditary myotonic syndromes

by V. P. Fedotov, S. A. Kurbatov, E. A. Ivanova, N. M. Galeeva, A. V. Polyakov
Published 2015-02-01

Clinical and genetic characteristics of autosomal recessive axonal neuropathy with neuromyotonia in Russian patients

by E. L. Dadali, S. S. Nikitin, S. A. Kurbatov, A. F. Murtazina, I. V. Sharkova, O. A. Shchagina, F. A. Konovalov
Published 2017-11-01

A case of hereditary motor and sensory neuropathy type IVA with unusual genealogy

by S. A. Kurbatov, T. B. Milovidova, V. P. Fedotov, A. F. Murtazina, G. E. Rudenskaya, O. A. Shchagina, A. V. Polyakov
Published 2018-07-01

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

by S. A. Kurbatov, P. G. Tsygankova, K. Yu. Mollaeva, I. O. Bychkov, Yu. S. Itkis, V. V. Zabnenkova, Z. R. Umakhanova, L. G. Geybatova, E. Yu. Zakharova
Published 2019-11-01

Clinical and genetic characteristics of Charcot–Marie–Tooth disease type 4D (type Lom) in Russia

by A. F. Murtazina, O. A. Shchagina, T. B. Milovidova, E. L. Dadali, G. E. Rudenskaya, S. A. Kurbatov, T. V. Fedotova, S. S. Nikitin, P. A. Sparber, M. D. Orlova, A. V. Polyakov
Published 2020-08-01