Zobrazeno 1 - 10
of 39
pro vyhledávání: '"S. V. Mikhaylova"'
Autor:
T. A. Gremyakova, S. B. Artemyeva, E. N. Baybarina, N. D. Vashakmadze, V. I. Guzeva, E. V. Gusakova, L. M. Kuzenkova, A. E. Lavrova, O. A. Lvova, S. V. Mikhaylova, L. P. Nazarenko, S. S. Nikitin, A. V. Polyakov, E. L. Dadali, A. G. Rumyantsev, G. E. Sakbaeva, V. M. Suslov, O. I. Gremyakova, A. A. Stepanov, N. I. Shakhovskaya
Publikováno v:
Нервно-мышечные болезни, Vol 13, Iss 2, Pp 10-19 (2023)
Duchenne muscular dystrophy is a genetic orphan neuromuscular disease caused by a mutation in the DMD gene encoding the protein dystrophin. As a result of developing and progressive muscle damage and atrophy, children lose the ability to walk, develo
Externí odkaz:
https://doaj.org/article/4f23ad2f44564dcc8bb335b99bdacb0e
Autor:
S. V. Mikhaylova
Publikováno v:
RUDN Journal of Medicine, Vol 24, Iss 2, Pp 183-190 (2020)
To characterize fitness health, defined as the state of the physical well-being of the body, due to the functional state, physical qualities and component composition of the body, assessment methods are needed. The purpose of the study : physiologica
Externí odkaz:
https://doaj.org/article/fb990cdddb2749aebcc93322a6140bd4
Autor:
E. Yu Voskoboeva, T. M. Bookina, A. N. Semyachkina, S. V. Mikhaylova, N. D. Vashakmadze, G. V. Baydakova, E. Yu Zakharova, S. I. Kutsev
Publikováno v:
Frontiers in Molecular Biosciences, Vol 8 (2022)
Mutations in the IDUA gene cause deficiency of the lysosomal enzyme alpha-l-iduronidase (IDUA), which leads to a rare disease known as mucopolysaccharidosis type I. More than 300 pathogenic variants of the IDUA gene have been reported to date, but no
Externí odkaz:
https://doaj.org/article/f8b01ae100a143058ab34fccabc7477d
Autor:
P. S. Orlov, V. N. Maksimov, S. V. Mikhaylova, D. E. Ivanoshchuk, S. K. Malyutina, M. I. Voevoda
Publikováno v:
Атеросклероз, Vol 15, Iss 3, Pp 50-55 (2019)
The aim of the study was to investigate the association of SNPs in the TRPA1 (rs13268757) and TRPV1 (rs222747) genes with myocardial infarction. Material and methods. Myocardial infarction (MI) (200 individuals) and control (420 individuals) group
Externí odkaz:
https://doaj.org/article/d3bf4117d739467db8412d69d81a73c7
Autor:
S. V. Mikhaylova, I. A. Pogrebnaya
Publikováno v:
Вестник Дагестанского государственного технического университета: Технические науки, Vol 46, Iss 2, Pp 20-27 (2019)
Objectives Investigate the prospect of improving the quality of centrifugal pumps in oil production.Method The method is based on energy-efficient installations for high-yield wells - the steps of the Borets-Weatherford installations and the Borets P
Externí odkaz:
https://doaj.org/article/dc81a1053b57417ba26395afef0cc81a
Autor:
E. L. Dadali, F. A. Konovalov, I. A. Akimova, A. A. Sharkov, G. E. Rudenskaya, S. V. Mikhaylova, S. A. Korostelev
Publikováno v:
Нервно-мышечные болезни, Vol 8, Iss 2, Pp 42-52 (2018)
Background. A large number of single gene disorders with seizures in clinical picture has been described. Among them, a special place is held by early-onset epileptic encephalopathies (EEE) – a genetically diverse group of disorders characterized b
Externí odkaz:
https://doaj.org/article/487b6c1732b74dbb99f5b14660251b6b
Autor:
M. Yu. Bobylova, V. S. Kakaulina, E. S. Il’ina, I. V. Nekrasova, N. L. Pechatnikova, S. V. Mikhaylova, M. B. Mironov, K. Yu. Mironov
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 9, Iss 2, Pp 39-46 (2017)
Dystonic hyperkinesias in children of early childhood may beinvolved in the structure of many syndromes that have differentetiological factors, prognosis, and treatment. This review presentsvarious clinical types of dystonias: benign idiopathic forms
Externí odkaz:
https://doaj.org/article/c1516c10273e4865ab72b5a2e5b2acad
Autor:
S. S. Nikitin, S. I. Kutsev, E. N. Basargina, S. V. Mikhaylova, E. Yu. Zakharova, V. I. Larionova, S. I. Polyakova, N. P. Kotlukova, E. N. Arkhipova, M. O. Kovalchuk, N. V. Buchinskaya
Publikováno v:
Нервно-мышечные болезни, Vol 6, Iss 1, Pp 11-43 (2016)
Externí odkaz:
https://doaj.org/article/e0cae3a787574e14abdbd6b1dc15e6db
Publikováno v:
Туберкулез и болезни лёгких, Vol 97, Iss 6, Pp 56-57 (2019)
Externí odkaz:
https://doaj.org/article/6c92f9e110834ac183d76526c7ab6d43
Autor:
T. D. Krylova, P. G. Tsygankova, Y. S. Itkis, N. L. Sheremet, T. A. Nevinitsyna, S. V. Mikhaylova, E. Y. Zakharova
Publikováno v:
Biochemistry (Moscow), Supplement Series B: Biomedical Chemistry. 12:43-49
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e6e20532f1caebdda54334568dc12d8
https://doi.org/10.1134/s1990750818010080
https://doi.org/10.1134/s1990750818010080