Zobrazeno 1 - 10
of 102
pro vyhledávání: '"R. V Deev"'
Autor:
A. V. Zholinsky, A. I. Kadykova, N. S. Gladyshev, M. V. Terekhov, A. A. Ivashechkin, V. V. Maksyutina, A. I. Nekrasova, S. I. Mitrofanov, M. V. Ivanov, D. A. Kashtanova, V. S. Yudin, A. A. Keskinov, S. M. Yudin, R. V. Deev, V. I. Skvortsova
Publikováno v:
Спортивная медицина: наука и практика, Vol 13, Iss 4, Pp 12-26 (2024)
Introduction: Morphofunctional changes of the circulatory system organs detected in athletes may remain without due attention, as clinical (phenotypic) signs of pathological abnormalities are very similar to manifestations of cardiovascular system ad
Externí odkaz:
https://doaj.org/article/0de727b8a0634cd9a1f4879f28582ed3
Publikováno v:
Спортивная медицина: наука и практика, Vol 12, Iss 4, Pp 59-66 (2023)
NGS is becoming an integral part of medical practice, including in cardiology. The role of genes in the formation of diseases of the cardiovascular system has been actively studied for the last 20 years. Currently, heart diseases with a hereditary co
Externí odkaz:
https://doaj.org/article/8398a434282b40e6a0ca2a8c9aad348a
Autor:
M. V. Korokin, E. V. Kuzubova, A. I. Radchenko, R. V. Deev, I. A. Yakovlev, A. V. Deikin, N. S. Zhunusov, A. M. Krayushkina, V. M. Pokrovsky, O. A. Puchenkova, K. D. Chaprov, N. V. Ekimova, S. N. Bardakov, O. N. Chernova, A. M. Emelin, I. S. Limaev
Publikováno v:
Фармация и фармакология (Пятигорск), Vol 10, Iss 5, Pp 483-496 (2022)
The aim of the work was behavioral and pathomorphological phenotyping of the mice knockout for the DYSF gene, which plays an important role in the development and progression of dysferlinopathy.Materials and methods. A B6.A-Dysfprmd/GeneJ (Bla/J) mic
Externí odkaz:
https://doaj.org/article/d38a67d29fb84df8b4112fa10beab58d
Autor:
S. N. Bardakov, I. S. Limaev, A. M. Emelin, V. Nikitins, E. V. Presnyakov, S. A. Kurbatov, P. G. Tsygankova, V. A. Tsargush, I. A. Chekmareva, E. V. Kolmakova, N. V. Bakulina, R. V. Deev
Publikováno v:
Нервно-мышечные болезни, Vol 12, Iss 4, Pp 56-72 (2022)
Mitochondrial neurogastrointestinal encephalomyopathy is an extremely rare (1–9:1 000 000, Orphanet, 2021) multisystem genetic disease caused by mutations in the TYMP gene encoding the enzyme thymidine phosphorylase.The article presents the data of
Externí odkaz:
https://doaj.org/article/18016ff039554d8791c0c23664fce85c
Autor:
S. N. Bardakov, A. М. Emelin, S. S. Nikitin, A. N. Khelkovskaya-Sergeeva, I. S. Limaev, A. F. Murtazina, V. A. Tsargush, M. V. Gusev, Ya. V. Safronova, V. S. Kaimonov, A. A. Isaev, R. V. Deev
Publikováno v:
Нервно-мышечные болезни, Vol 12, Iss 4, Pp 73-87 (2022)
Differential diagnosis of inflammatory myopathies with hereditary muscular dystrophies accompanied by a secondary inflammatory process is a time‑consuming clinical and pathomorphological task. In particular, false diagnosis of polymyositis in patie
Externí odkaz:
https://doaj.org/article/b2e69f02488b40eaa34fb3cd3cd8b162
Publikováno v:
Спортивная медицина: наука и практика, Vol 12, Iss 2, Pp 82-95 (2022)
There are many classifications of sports disciplines, which base on various approaches, which separately take into account the patterns of training activity, physiology, the risk of collision and injury, etc. In our opinion, it most fully reflects th
Externí odkaz:
https://doaj.org/article/eb3a51cf48eb4eeea281f4c9c1fff1c7
Autor:
O. Ya. Porembskaya, V. N. Kravchuk, M. I. Galchenko, R. V. Deev, M. Sh. Chesnokov, A. V. Avanesyan, K. V. Lobastov, S. N. Tsaplin, L. A. Laberko, V. S. Ermakov, O. V. Pashovkina, I. V. Schastlivtsev, S. A. Sayganov
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 18, Iss 4, Pp 376-384 (2022)
Aim. We aimed to study the histological and thrombotic changes in lung vessels in patients who died with COVID-19, to access the correlation between anticoagulation therapy (ACT) and thrombotic events (TE), treatment results, clinical and laboratory
Externí odkaz:
https://doaj.org/article/99acba87ea4c4f0b9d67721093498754
Autor:
A. V. Zholinsky, A. I. Kadykova, V. S. Feshchenko, M. G. Hovhannisyan, A. V. Zorenko, R. V. Deev
Publikováno v:
Спортивная медицина: наука и практика, Vol 11, Iss 4, Pp 5-16 (2022)
Molecular genetic methods are an integral part of recent medicine. Polymerase chain reaction, Sanger sequencing, next-generation sequencing are widely used in many areas: diagnostics of infectious, inherited, oncological diseases, prenatal screening,
Externí odkaz:
https://doaj.org/article/c39f0a069e284a068e0009428b7f1d62
Autor:
S. S. Nikitin, S. N. Bardakov, N. A. Suponeva, I. V. Zhirov, T. A. Adyan, D. A. Grishina, R. V. Deev
Publikováno v:
Нервно-мышечные болезни, Vol 11, Iss 3, Pp 12-36 (2021)
Transthyretin amyloidosis (ATTR-amyloidosis) is a systemic progressive fatal disease, for which a modifying therapy has recently been proposed that delays the progression of the disease and improves the patient’s quality of life. The delay in the d
Externí odkaz:
https://doaj.org/article/2c8b6b89032e4c1b888806a2edc307f7
Autor:
S. N. Bardakov, D. I. Skulyabin, A. N. Moshnikova, S. V. Lapin, A. A. Sokolov, E. A. Kondratyeva, T. V. Bulgakova, A. S. Manuilov, M. V. Zakharov, A. N. Belskikh, V. A. Tsargush, R. V. Deev
Publikováno v:
Нервно-мышечные болезни, Vol 11, Iss 4, Pp 34-47 (2021)
Anti‑NMDA encephalitis is a rare autoimmune disease of the central nervous system caused by the synthesis of autoantibodies to the NR1/NR2 subunits of the NMDA receptor, characterized by the development of acute mental, cognitive, motor, autonomic
Externí odkaz:
https://doaj.org/article/bd93456b2bc34e9b8f43fedc37308e55