Zobrazeno 1 - 10
of 88
pro vyhledávání: '"L. M. Kuzenkova"'
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:
T. A. Gremyakova, S. V. Artemyeva, N. D. Vashakmadze, I. P. Vitkovskaya, V. I. Guzeva, O. V. Guzeva, L. M. Kuzenkova, S. V. Mikhailova, L. P. Nazarenko, T. M. Pervunina, N. L. Pechatnikova, T. V. Podkletnova, G. E. Sakbaeva, A. A. Stepanov, V. M. Suslov, O. I. Gremyakova, N. I. Shakhovskaya, S. S. Nikitin
Publikováno v:
Нервно-мышечные болезни, Vol 12, Iss 2, Pp 10-18 (2022)
Duchenne muscular dystrophy (DMD) is a fatal neuromuscular disease due to a mutation in the gene encoding dystrophin synthesis. In patients, muscle damage and atrophy progresses, the ability to move independently decreases as well as respiratory and
Externí odkaz:
https://doaj.org/article/2d5cb1f3844a45cb95295db2a3337785
Autor:
A. L. Kurenkov, L. M. Kuzenkova, B. I. Bursagova, V. V. Chernikov, O. V. Agranovich, L. G. Khachatryan, V. M. Kenis, V. A. Zherebtsova, M. N. Sarzhina, N. D. Odinaeva, A. R. Artemenko, G. A. Popova, E. A. Moroshek, E. E. Tabe, A. A. Nezhelskaya, A. A. Maksimenko, L. Ya. Akhadova, M. V. Indereikin, N. V. Duibanova, L. V. Tikhonova, A. V. Sapogovskiy, Z. M. Gadzhialieva, A. V. Grigorieva, V. S. Perminov, I. D. Fedonyuk, L. M. Kolpakchi, A. Yu. Kursakova, N. A. Tsurina
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 14, Iss 2, Pp 117-125 (2022)
Botulinum therapy for cerebral palsy (CP) is considered not only as one of the effective approaches for the treatment of increased muscle tone and spasticity, but also as a method of excessive salivation correction. The article presents an overview o
Externí odkaz:
https://doaj.org/article/9d0b5cf529ef41c19d59bbf356c0c69c
Autor:
A. L. Kurenkov, L. M. Kuzenkova, V. V. Chernikov, B. I. Bursagova, A. A. Nezhelskaya, A. R. Artemenko
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 13, Iss 4, Pp 52-59 (2021)
Sialorrhea is a severe medical problem that is difficult to treat, which can lead to serious complications. In almost all cases, chronic sialorrhea is accompanied by a restriction of the child's contacts with peers, socialization difficulties, and a
Externí odkaz:
https://doaj.org/article/738d246fce0c4e50a18745eae0705cea
Autor:
S. B. Artemieva, L. M. Kuzenkova, E. S. Ilyina, Yu. A. Kursakova, L. M. Kolpakchi, E. Yu. Sapego, A. A. Golenko, S. G. Popovich, D. V. Parshin, O. A. Shidlovskaya, Yu. O. Papina, A. V. Monakhova, D. V. Vlodavets
Publikováno v:
Нервно-мышечные болезни, Vol 10, Iss 3, Pp 35-41 (2020)
Introduction. Spinal muscular atrophy is a severe neuromuscular disease characterized by rapid progression of muscle weakness and early death. Pathogenetic therapy with nusinersen can significantly change the course of the disease and enable the pati
Externí odkaz:
https://doaj.org/article/d4d807ba23b9488ebcb489a0ed528e87
Autor:
A. L. Kurenkov, O. A. Klochkova, B. I. Bursagova, L. M. Kuzenkova, A. R. Artemenko, I. V. Falkovsky
Publikováno v:
Медицинский совет, Vol 0, Iss 1S, Pp 113-121 (2017)
Injections of botulinum toxin type A (BTA) are regarded as one of the basic methods to treat cerebral palsy (CP). The article discusses issues unique mechanism of action of botulinum toxin type A injections, double sensomotor mechanism of action of t
Externí odkaz:
https://doaj.org/article/d5666562bf6d4bf5b8f4167125496e53
Publikováno v:
Педиатрическая фармакология, Vol 13, Iss 3, Pp 251-258 (2016)
Background: Specialized foods, based on aminoacids without phenilalanin, are the main source of protein for patients with phenilketonuria of all ages. Based on modern technologies, new Russian-made foods were created. They have an optimized aminoacid
Externí odkaz:
https://doaj.org/article/76bac02d888b4e83975a08c89e6a2bc1
Autor:
O. A. Klochkova, A. L. Kurenkov, K. M. Karimova, B. I. Bursagova, L. S. Namazova-Baranova, A. M. Mamedyarov, L. M. Kuzenkova, I. M. Tardova, I. V. Fal’kovskiy, O. G. Dontzov, M. A. Ryzhenkov, V. A. Zmanovskaya, M. N. Butorina, O. L. Pavlova, N. N. Harlamova, D. M. Dankov, E. V. Levitina, D. A. Popkov, S. O. Ryabykh, S. N. Medvedeva, E. B. Gubina, L. N. Vladykina, V. M. Kenis, T. I. Kiseleva, D. A. Krasavina, O. N. Vasil’eva, A. S. Nosko, V. P. Zykov, V. I. Michnovich, T. A. Belogorova, L. V. Rychkova
Publikováno v:
Педиатрическая фармакология, Vol 13, Iss 3, Pp 259-269 (2016)
Background: The contemporary application of Botulinum toxin A (BTA) in cerebral palsy (CP) implies multilevel injections both in on-label and off-label muscles. However, there is no single international opinion on the effective and safe dosages, targ
Externí odkaz:
https://doaj.org/article/8311b1c0bf284d4290f52f9a2060867b
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 6, Iss 1, Pp 57-63 (2016)
Abstract: the article present the literature data on clinical, EEG characteristics of benign occipital epilepsy of childhood with early debut – Panayiotopoulos syndrome, and the results of own research group of patients with this form of idiopathic
Externí odkaz:
https://doaj.org/article/0c28316c764943d0b3767362f7af4774
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 6, Iss 2, Pp 52-60 (2016)
Abstract: this article contains information about the principles of treatment different forms of epilepsy and a more detailed information about antiepileptic drug - topiramate. Based on the own research the authors evaluate the efficacy and safety of
Externí odkaz:
https://doaj.org/article/7d2050004ab542a28fccdeecebaddabf