Spinal Muscular Atrophy 5q under the Mask of Myopathy: 10 Clinical Cases by Sergei A. Kurbatov

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The Legend of “berendeika”. Historical and Linguistic Note by Dr. Oleg A. Kurbatov

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Late-onset Pompe disease with phenotype of the limb-girdle muscular dystrophy by S. A. Kurbatov, S. S. Nikitin, E. Yu. Zakharova

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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

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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

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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

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Assessment of heavy metals content in podzolic soil for various granulometric composition when applying activated sludge as the basis for nanofertilizer (the pulp-and-paper indu... by Maria G. Yurkevich, Ruslan R. Suleymanov, Ekaterina S. Dorogaya, Arkady A. Kurbatov

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Electrodeposition of Mo/MoOx on Copper Substrate from Dimethyl Sulfoxide Solutions by A. Dauletbay, W. Braida, M. Nauryzbaev, L. Kudreeva, A. Kurbatov, A. Tulegenov

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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

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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

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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

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A case of myotonic dystrophy type 1 with paternal history of clinical worsening by S. A. Kurbatov, V. P. Fedotov, N. M. Galeeva, V. V. Zabnenkova, A. V. Polyakov

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Myotonic dystrophy: genetics and clinical polymorphism by Ekaterina O. Ivanova, Anna N. Moskalenko, Ekaterina Yu. Fedotova, Sergey A. Kurbatov, Sergey N. Illarioshkin

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Juvenile Huntington’s disease by G. E. Rudenskaya, D. A. Savvin, V. P. Fedotov, S. A. Kurbatov, A. V. Polyakov, N. M. Galeeva

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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

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Galileo E5 AltBOC Signals: Application for Single-Frequency Total Electron Content Estimations by Artem M. Padokhin, Anna A. Mylnikova, Yury V. Yasyukevich, Yury V. Morozov, Gregory A. Kurbatov, Artem M. Vesnin

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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

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Temperature Dependent Characteristics of Activated Carbons from Walnut Shells for Improved Supercapacitor Performance by V. V. Pavlenko, Q. Abbas, P. Przygocki, T. Kon’kova, Zh. Supiyeva, N. Abeykoon, N. Prikhodko, M. Bijsenbayev, A. Kurbatov, B.T. Lesbayev, Z. A. Mansurov

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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

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SPECTRUM OF MOLECULAR GENETIC ALTERATIONS AND DIVERSITY OF CLINICAL FORMS OF STARGARDT DISEASE by N. L. Sheremet, I. G. Grushke, N. V. Zhorzholadze, I. A. Ronzina, A. A. Mikaelyan, S. A. Kurbatov, V. V. Kadyshev, K. I. Anoshkin, V. V. Strelnikov

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