Mitochondrial DNA maintenance disorders in 102 patients from different parts of Russia: Mutational spectrum and phenotypes
Bychkov, I.O., Itkis, Y.S., Tsygankova, P.G., Krylova, T.D., Mikhaylova, S.V., Klyushnikov, S.A., Pechatnikova, N.L., Degtyareva, A.V., Nikolaeva, E.A., Seliverstov, Y.A., Kurbatov, S.A., Dadali, E.L., Rudenskaya, G.E., Illarioshkin, S.N., Zakharova, E.Y.
Published in Mitochondrion (01.03.2021)
Published in Mitochondrion (01.03.2021)
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Journal Article
Recent Problems of Heat-Transfer Simulation in Technological Processes of Selective Laser Melting and Fusion
Zhavoronok, S. I., Kurbatov, A. S., Rabinskiy, L. N., Solyaev, Yu. O.
Published in High temperature (01.11.2019)
Published in High temperature (01.11.2019)
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Journal Article
Myotonia and myotonic discharges of dystrophic myotonia type 1 at the first decade onset: a literature review and data of the case series
Kurbatov, S. A., Kenis, V. M., Savina, M. V., Kleimenova, I. S., Priymak, N. S., Kryukov, Yu. V., Kokorina, A. A., Ryadninskaya, N. V., Kuznetsova, I. A., Shchagina, O. A., Poliakov, A. V.
Published in Nervno-myshechnye bolezni (09.06.2022)
Published in Nervno-myshechnye bolezni (09.06.2022)
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Journal Article
A new mutation in the TYMP-gene: clinical and morphological characteristics of a patient with MNGIE syndrome
Bardakov, S. N., Limaev, I. S., Emelin, A. M., Nikitins, V., Presnyakov, E. V., Kurbatov, S. A., Tsygankova, P. G., Tsargush, V. A., Chekmareva, I. A., Kolmakova, E. V., Bakulina, N. V., Deev, R. V.
Published in Nervno-myshechnye bolezni (13.12.2022)
Published in Nervno-myshechnye bolezni (13.12.2022)
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Journal Article
Clinical and genetic characteristics of Charcot–Marie–Tooth disease type 4D (type Lom) in Russia
Murtazina, A. F., Shchagina, O. A., Milovidova, T. B., Dadali, E. L., Rudenskaya, G. E., Kurbatov, S. A., Fedotova, T. V., Nikitin, S. S., Sparber, P. A., Orlova, M. D., Polyakov, A. V.
Published in Nervno-myshechnye bolezni (23.08.2020)
Published in Nervno-myshechnye bolezni (23.08.2020)
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Journal Article
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. Yu, Bychkov, I. O., Itkis, Yu. S., Zabnenkova, V. V., Umakhanova, Z. R., Geybatova, L. G., Zakharova, E. Yu
Published in Nervno-myshechnye bolezni (20.11.2019)
Published in Nervno-myshechnye bolezni (20.11.2019)
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Journal Article
Late-onset Pompe disease with phenotype of the limb-girdle muscular dystrophy
Kurbatov, S. A., Nikitin, S. S., Zakharova, E. Yu
Published in Nervno-myshechnye bolezni (21.09.2015)
Published in Nervno-myshechnye bolezni (21.09.2015)
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Journal Article
A case of Becker myotonia with pseudodominant inheritance: сurrent approaches to the differential diagnosis of Thomsen’s and Becker's myotonia congenita
Kurbatov, S. A., Nikitin, S. S., Illarioshkin, S. N., Gundorova, P., Polyakov, A. V.
Published in Nervno-myshechnye bolezni (29.03.2016)
Published in Nervno-myshechnye bolezni (29.03.2016)
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