Zobrazeno 1 - 5
of 5
pro vyhledávání: '"I. V. Shulyakova"'
Autor:
S. B. Artemyeva, O. A. Shidlovskaya, Yu. O. Papina, A. V. Monakhova, I. V. Shulyakova, E. D. Belousova, O. Yu. Germanenko, D. V. Vlodavets
Publikováno v:
Нервно-мышечные болезни, Vol 14, Iss 1, Pp 86-92 (2024)
Spinal muscular atrophy (SMA) is a hereditary, autosomal recessive disease that debuts at different ages. Neurological symptoms are progressive and lead to significant limitation of life activity and reduced life expectancy. Currently, there are seve
Externí odkaz:
https://doaj.org/article/f2f91c0cc52a4187a0a0049cebda1a23
Autor:
T. G. Okhapkina, Z. K. Gorchanova, I. V. Shulyakova, E. S. Ilyina, E. S. Michurina, E. D. Belousova
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 9, Iss 2, Pp 74-90 (2017)
West syndrome is an epileptic syndrome, characterized by a triad of symptoms: infantile spasms, hypsarrhythmia on interictal EEG, and a regression or delay of psycho-motoric development. According to the current concept, two of these three criteria s
Externí odkaz:
https://doaj.org/article/e90e6c7cc3294517bbf9f228ddfe6fe1
Autor:
E. D. Belousova, Z. K. Gorchanova, E. S. Michurina, E. S. Ilyina, T. G. Okhapkina, I. V. Shulyakova
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 9, Iss 2, Pp 74-90 (2017)
West syndrome is an epileptic syndrome, characterized by a triad of symptoms: infantile spasms, hypsarrhythmia on interictal EEG, and a regression or delay of psycho-motoric development. According to the current concept, two of these three criteria s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1a6bd6847ad18ea181f11b97b291319
https://doi.org/10.17749/2077-8333.2017.9.2.074-090
https://doi.org/10.17749/2077-8333.2017.9.2.074-090
Autor:
T. I. Baranich, S. B. Artemyeva, N. V. Kleimenova, L. A. Khavkhun, D. V. VIodavets, D. O. Kazakov, P. A. Shatalov, E. B. Litvinova, I. V. Shulyakova, A. V. Brydun, V. V. Glinkina, V. S. Sukhorukov
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 60, Iss 4, Pp 69-74 (2016)
The clinical presentation of progressive limb-girdle muscular dystrophy type 2A (LGMD2A) is due to loss of functionally active cal-pain-3, a skeletal muscle specific isoform of one of the calpain family proteins involved in the regulation of differen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::e43b33921e26c7a0e56a9c458cf5b1f1
https://www.ped-perinatology.ru/jour/article/view/138
https://www.ped-perinatology.ru/jour/article/view/138
Publikováno v:
Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova. 116:61
West syndrome is one of the most well-known epileptic encephalopathies, a catastrophic epilepsy syndrome with onset in the first year of life. Prognosis of this condition depends on the etiology and adequate treatment. The authors review the hormonal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b019fcb2d267f445383f51e958e1edaf
https://doi.org/10.17116/jnevro20161169261-66
https://doi.org/10.17116/jnevro20161169261-66