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pro vyhledávání: '"Olga V. Petryaeva"'
Autor:
Natalia A. Shnayder, Olga V. Petryaeva, Ivan P. Artyuhov, Margarita R. Sapronova, Irina O. Loginova
Publikováno v:
International Journal of Biomedicine, Vol 7, Iss 4, Pp 324-326 (2017)
Charcot-Marie-Tooth disease type 2 (CMT2S) is rare form of Charcot-Marie-Tooth disease (CMT) that is characterized by a mutation in the IGHMBP2 gene. This gene encodes a helicase superfamily member that binds a specific DNA sequence from the region o
Externí odkaz:
https://doaj.org/article/049c478e6aca4ed1bf34728af317fc6f
Autor:
Olga V. Petryaeva, Irina O. Loginova
Publikováno v:
Психология. Психофизиология. 12:34-43
Considering research on rehabilitation and rehabilitation potential in modern medical and psychological literature from the leading databases reduces subjectivity when analyzing the relevance of scientific issues. The results obtained will allow pred
Autor:
Olga V. Petryaeva, Irina O. Loginova
Publikováno v:
Psychological Applications and Trends 2021.
Statement of the problem. The article formulates the problem and purpose of a study focused on identifying the characteristics of the doctors life-world stability during the pandemic associated with COVID-19. The problem of this study is due to the c
Publikováno v:
Psychological Applications and Trends 2021.
"Staying at the peak of professional success in medical is possible only for a doctor who is characterized by psychological health. The human life-world stability is contributed to success of the life self-fulfillment and transference of abilities in
Autor:
Natalia Shnayder, Irina O. Loginova, Olga V. Petryaeva, Ivan Artyukhov, Margarita R. Sapronova
Publikováno v:
Journal of Biosciences and Medicines. :23-34
Charcot-Marie-Tooth (CMT) disease, which encompasses several hereditary motor and sensory neuropathies, is one of the most common neuro-muscular disorders. 80% of patients having CMT disease are diagnosed with per cavus deformity. Orthosis is widespr
Autor:
Margarita R. Sapronova, Irina O. Loginova, Olga V. Petryaeva, Ivan Artyuhov, Natalia Shnayder
Publikováno v:
International Journal of Biomedicine, Vol 7, Iss 4, Pp 324-326 (2017)
Charcot-Marie-Tooth disease type 2 (CMT2S) is rare form of Charcot-Marie-Tooth disease (CMT) that is characterized by a mutation in the IGHMBP2 gene. This gene encodes a helicase superfamily member that binds a specific DNA sequence from the region o