Zobrazeno 1 - 10
of 85
pro vyhledávání: '"L. M. Kuzenkova"'
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:
D. V. Vlodavets, N. V. Ganina, E. S. Ilina, A. A. Kokorina, L. M. Kuzenkova, E. Yu. Sapego, D. S. Smirnov, Yu. A. Shevtsova, A. V. Saulina, A. N. Petrov, N. A. Zolkin, Yu. N. Linkova, A. V. Zinkina-Orikhan
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 66, Iss 4, Pp 64-73 (2021)
Objective. To analyze the natural course of type 1 spinal muscular atrophy in children with the onset of the disease up to 6 months in the Russian population.Material and methods. The retrospective multicenter study included data of 54 children with
Externí odkaz:
https://doaj.org/article/f70391724f154e2ba1f5c21b766216e9
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
Autor:
N. D. Vashakmadze, L. S. Namazova-Baranova, A. K. Gevorkyan, L. M. Kuzenkova, T. V. Podkletnova, M. A. Babaikina, A. V. Anikin, G. V. Kuznetsova, L. A. Osipova
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 61, Iss 4, Pp 114-120 (2016)
Joint pathology without signs of inflammation must always arouse suspicion of lysosomal storage diseases, mucopolysaccharidosis (MPS) in particular. It is these orthopedic diseases in mild MPS type I, which are an early sign of the disease; moreover,
Externí odkaz:
https://doaj.org/article/51bdde6c02e5480789d1be7781f7167f
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
Publikováno v:
Вопросы современной педиатрии, Vol 14, Iss 6, Pp 724-731 (2016)
Leukoencephalopathy with predominant lesion of the brain stem, spinal cord and high blood lactate in the MR spectroscopy is a hereditary disease characterized by slowly progressing cerebellar, pyramidal disorders, disorders involving the lesion of po
Externí odkaz:
https://doaj.org/article/1732dacf7d79472fb4a4b0bc75e241dd