Zobrazeno 1 - 10
of 91
pro vyhledávání: '"D. A. Rudenko"'
Publikováno v:
International Journal of Polymer Science, Vol 2013 (2013)
The optical and bactericidal properties of acetic and basic chitosan films were studied. By the ORD technique, we found that these films differed in the values of their specific optical rotation and of their rotary and dispersive constants. A sign in
Externí odkaz:
https://doaj.org/article/1ec19bbdff6143b6baa51d8e03270f6a
Publikováno v:
Нервно-мышечные болезни, Vol 13, Iss 4 (2024)
Background. Duchenne muscular dystrophy is a hereditary, X-linked, progressive, disabling disease. One of the possible pathogenetic methods for treating this disease is the drug ataluren, which acts at the stage of protein translation in the ribosome
Externí odkaz:
https://doaj.org/article/f22fc8205d2e469ead6ae1a53dc548f4
Publikováno v:
Креативная хирургия и онкология, Vol 12, Iss 3, Pp 256-260 (2022)
Introduction. Hepatocellular carcinoma is oft en asymptomatic in its early stages and when the tumor is small. Though this type of tumor is oft en accompanied with metastasis to the lungs, the present paper describes a patient whose both pathologies
Externí odkaz:
https://doaj.org/article/e5f7cfe0b19c403ab01aad14626eede1
Autor:
V. M. Suslov, L. N. Lieberman, P. G. Carlier, G. N. Ponomarenko, D. O. Ivanov, D. I. Rudenko, G. A. Suslova, E. I. Adulas
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
Duchenne muscular dystrophy (DMD) is one of the most common forms of hereditary muscular dystrophies in childhood and is characterized by steady progression and early disability. It is known that physical therapy can slow down the rate of progression
Externí odkaz:
https://doaj.org/article/377f5c44e19e458881b8d4fab1e0ccb6
Autor:
R. A. Gapeshin, E. R. Barantsevich, D. I. Rudenko, T. R. Stuchevskaya, E. A. Gavrilova, M. S. Pushkaryov, A. A. Yakovlev, A. V. Gavrichenko, A. G. Smochilin
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 13, Iss 1, Pp 51-56 (2021)
Chronic inflammatory demyelinating polyneuropathy (CIDP) is a peripheral neuropathy, predominantly motor neuropathy, with a progressive or relapse-remitting course. Fatigue is a condition characterized by a physical or mental feeling of lack of energ
Externí odkaz:
https://doaj.org/article/a59f38639eea41a7b615192d25d17b0b
Autor:
V. Yu. Kudryashova, N. B. Lutova, D. I. Rudenko, A. Ya. Vuks, T. R. Stuchevskaya, O. D. Egorova, N. K. Kulagina, S. M. Zatakovenko
Publikováno v:
Обозрение психиатрии и медицинской психологии имени В.М. Бехтерева, Vol 0, Iss 4, Pp 33-41 (2020)
The aim of the study was self-regulation of behavior and other psychological aspects of adaptive-compensatory mechanisms in patients with schizophrenia and myasthenia, in comparison with a group of healthy subjects.Materials and methods. The study in
Externí odkaz:
https://doaj.org/article/cdea2db9809741f28ee77e0dfde61311
Publikováno v:
Нервно-мышечные болезни, Vol 10, Iss 1, Pp 53-63 (2020)
Introduction. Myasthenia gravis is one of the most common autoimmune neuromuscular diseases, the peak incidence is in the age of 20–40 years. However, studies show that throughout the world in recent decades there has been an increase in the preval
Externí odkaz:
https://doaj.org/article/f613dc435e504f739f662c0b756f813b
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 12, Iss 3, Pp 24-29 (2020)
Chronic inflammatory demyelinating polyneuropathy (CIDP) in patients with diabetes mellitus (DM) occurs approximately 9—11 times more frequently than in the general population.Objective: to assess the characteristics of CIDP in the presence of DM.P
Externí odkaz:
https://doaj.org/article/e26d645f89c44ae69efadad25021ac0e
Autor:
O. V. Melnik, A. B. Malashicheva, Yu. V. Fomicheva, A. A. Khudyakov, A. Ya. Gudkova, D. I. Rudenko, M. A. Simonenko, Е. N. Mikhailov, D. S. Lebedev, E. S. Vasichkina, T. M. Pervunina, A. A. Kostareva
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 72-77 (2019)
Mutations in the LMNA gene cause developing of several phenotypes, both with isolated involvement of cardiac, muscle, adipose and bone tissues, and with their combination. The dominance of cardiovascular signs in the clinical performance and false cl
Externí odkaz:
https://doaj.org/article/36befde99f054c6d88dfee7d1ca3a85b
Publikováno v:
Нервно-мышечные болезни, Vol 9, Iss 2, Pp 21-29 (2019)
Diagnosis of neuromuscular diseases is complicated by the variety of clinical manifestations and requires the use of additional methods, an important place among which is the pathomorphological study of skeletal muscle biopsy. Despite the fact that t
Externí odkaz:
https://doaj.org/article/a777cce2b90a445c9031433571e6fa76