Zobrazeno 1 - 10
of 132
pro vyhledávání: '"A. Prityko"'
Publikováno v:
Русский журнал детской неврологии, Vol 17, Iss 4, Pp 8-23 (2023)
Background. Currently, more than 500 genes are known, in one degree or another associated with the development of the phenotype of congenital cerebral palsy (CP). The amount of accumulated data requires the sorting of the mechanisms of the influence
Externí odkaz:
https://doaj.org/article/dea5b805787a4b0bb365e04bef08a9df
Publikováno v:
Русский журнал детской неврологии, Vol 17, Iss 3, Pp 43-54 (2022)
Background. The problem of congenital cerebral palsy (CP) is relevant due to the limited complexity of habilitation and social adaptation of such patients. The genetic aspects of the pathogenesis of the disease are being actively studied. CP is often
Externí odkaz:
https://doaj.org/article/3ed36bc9d21c4a68bba51e366d05ca84
Autor:
T. V. Kozhanova, S. S. Zhilina, T. I. Meshсheryakova, N. P. Prokopyeva, A. G. Prityko, N. N. Zavadenko
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 14, Iss 2, Pp 214-220 (2022)
The clinical case of a patient with congenital contractures of the lower and upper limbs, face, seizures, facial dysmorphias, motor disorders and psychomotor development delay is presented. The proband with Freeman–Sheldon syndrome had no mutations
Externí odkaz:
https://doaj.org/article/d61d98af154d4c0ca2e75248fdc73c27
Autor:
O.Y. Kovalenko, N.G. Prityko
Publikováno v:
Клінічна та профілактична медицина, Iss 1, Pp 21-27 (2022)
Relevance: The problem of treatment of cerebrovascular diseases is one of the leading in modern medicine. The combination of this nosology in patients with emotional and volitional disorders acquires a special shade. Features of neurochemical transmi
Externí odkaz:
https://doaj.org/article/a1febf1694c4433cbe16b204fe20d73a
Autor:
T. V. Kozhanova, S. S. Zhilina, T. I. Mescheryakova, M. Yu. Shorina, I. F. Demenshin, G. G. Prokopiev, I. V. Kanivets, V. S. Suchorukov, P. L. Anufriev, T. I. Baranich, A. A. Kozina, A. G. Prityko
Publikováno v:
Нервно-мышечные болезни, Vol 11, Iss 3, Pp 51-63 (2021)
Congenital muscular dystrophies are heterogeneous groups of neuromuscular diseases leading to hypotonia, progressive muscle weakness and dystrophic or structural signs in muscle biopsy. At the present time, 34 genes associated with congenital muscula
Externí odkaz:
https://doaj.org/article/01099aa7c969436698e9e63a4c653882
Akademický článek
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Publikováno v:
Русский журнал детской неврологии, Vol 16, Iss 3, Pp 46-54 (2021)
Background. The problem of preventing the development of gross congenital brain lesions and their successful treatment is more than relevant now. It is known that approximately in every third case of the development of congenital cerebral palsy (CP),
Externí odkaz:
https://doaj.org/article/e65f24dcad844e1983c1c6ab0422960f
Autor:
A. G. Prityko, K. V. Osipova, P. L. Sokolov, E. A. Ezhova, I. G. Kotel’nikova, E. G. Lukyanov, G. A. Osipova
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 13, Iss 3, Pp 200-210 (2021)
Objective: to prove the therapeutic equivalence and similar safety profile of “Sibazon, rectal solution” (international nonproprietary name: diazepam) and “Sibazon, solution for intravenous and intramuscular administration” in children with p
Externí odkaz:
https://doaj.org/article/a8dde0c082b2440999bb7287cb5c8145
Autor:
A. G. Prityko, K. V. Osipova, P. L. Sokolov, E. A. Ezhova, I. G. Kotel’nikova, E. G. Lukyanova, G. A. Osipova
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 13, Iss 2, Pp 97-105 (2021)
Objective: to confirm a therapeutic equivalence and similar safety profile of “Midazolam, oromucosal (buccal) solution” and “Sibazon, solution for intravenous and intramuscular administration” used in children aged from 1 year to 18 years suf
Externí odkaz:
https://doaj.org/article/3fbef71389ca4a91b32efc9dedd2c4a4
Autor:
T. V. Kozhanova, S. S. Zhilina, T. I. Meshcheryakova, E. G. Luk’yanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko, N. N. Zavadenko
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 13, Iss 1, Pp 44-50 (2021)
We present the clinical case of patient with epilepsy, developmental retardation and hearing loss. The whole exome sequencing allowed to reveal compound heterozygous variants of the nucleotide sequence in SPATA5 gene (c.1714+1G>A, c.1678G>A). Mutatio
Externí odkaz:
https://doaj.org/article/20cde55ee1614d86af7a31769b6e9d00