Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Alexey L. Kurenkov"'
Autor:
Inga V. Anisimova, Svetlana B. Artemyeva, Elena D. Belousova, Nato D. Vashakmadze, Dmitriy V. Vlodavets, Tatiana A. Gremyakova, Olga S. Groznova, Valentina I. Guzeva, Elena V. Gusakova, Lyudmila M. Kuzenkova, Alexey L. Kurenkov, Sergey I. Kutsev, Svetlana V. Mikhaylova, Lyudmila P. Nazarenko, Sergey S. Nikitin, Artem Yu. Novikov, Tatiana V. Podkletnova, Elena V. Polevichenko, Alexander V. Polyakov, Gennady G. Prokopyev, Dmitry I. Rudenko, Svetlana A. Repina, Evgeniia V. Romanenko, Sergey O. Ryabykh, Gul’zhan E. Sakbaeva, Elena Yu. Sapego, Liliia R. Selimzyanova, Andrey A. Stepanov, Dmitry M. Subbotin, Vasiliy M. Suslov, Elena V. Tozliyan, Dmirty A. Feklistov, Nadezhda I. Shakhovskaya, Ekaterina V. Shreder
Publikováno v:
Педиатрическая фармакология, Vol 20, Iss 5, Pp 427-453 (2023)
Duchenne muscular dystrophy is one of the most common forms of childhood muscular dystrophies. Its incidence is 1 in 3.5–6 thousand newborn boys according to various sources. The disease is caused by the mutation in the DMD gene coding the dystroph
Externí odkaz:
https://doaj.org/article/376b5dfeb86d48aa82f78ab3af2f103f
Autor:
Olga A. Klochkova, Alexey L. Kurenkov
Publikováno v:
Вопросы современной педиатрии, Vol 19, Iss 2, Pp 107-115 (2020)
Various aspects of muscle strength decrease and loss of motor skills in patients with cerebral palsy (CP) are considered in this review. Pathophysiological mechanisms caused by primary damage and reorganization of central nervous system (CNS), struct
Externí odkaz:
https://doaj.org/article/3ffbf8a7aaab4e3a95a6f35a19b820d7
Autor:
Olga A. Klochkova, Alexey L. Kurenkov, Natalya V. Zhurkova, Kirill V. Savostyanov, Ilya S. Zhanin, Ayaz M. Mamedyarov, Ilona M. Tardova
Publikováno v:
Вопросы современной педиатрии, Vol 16, Iss 4, Pp 326-333 (2017)
Autosomal recessive peripheral neuropathy with neuromyotonia (ARAN-NM) is a relatively newly described disease associated with mutations in the HINT1 gene. It accounts for a significant part of the poorly differentiated forms of axonal polyneuropathi
Externí odkaz:
https://doaj.org/article/1e08c8c623fc4af59ecbada229c00dea
Autor:
Olga A. Klochkova, Alexey L. Kurenkov, Leyla S. Namazova-Baranova, Ayaz M. Mamedyarov, Khadizhat M. Karimova, Margarita A. Kuznetsova
Publikováno v:
Вопросы современной педиатрии, Vol 16, Iss 1, Pp 39-48 (2017)
The botulinum therapy remains the most effective and safe method for reducing local spasticity in patients with cerebral palsy (CP). However, the list of indications for injections of botulinum toxin type A (BTA) in cerebral palsy is limited both in
Externí odkaz:
https://doaj.org/article/94ba920ce8764658aefa55bb18fbadaa
Publikováno v:
L.O. Badalyan Neurological Journal. 4:43-51
Multiple sclerosis (MS) is a rare neuroinflammatory and neurodegenerative disease that leads to disability and a significant decrease in the quality of life. Over the past decade, the focus of studies of MS disease-modifying therapies (DMT) in adults
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02eff04a6f96193053f67653325c6692
https://doi.org/10.46563/2686-8997-2023-4-1-43-51
https://doi.org/10.46563/2686-8997-2023-4-1-43-51
Autor:
Tatyana V. Podkletnova, Lyudmila M. Kuzenkova, Alexey L. Kurenkov, Evgeniya V. Uvakina, Sofya G. Popovich, Anastasiya A. Lyalina
Publikováno v:
L.O. Badalyan Neurological Journal. 3:96-100
Duchenne muscular dystrophy (DMD) is a hereditary progressive muscular dystrophy with an X-linked recessive type of inheritance, mainly manifested in boys, characterized by an onset at an early age, rapidly progressive atrophy of the striated muscles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d93bd7e3a220c01af27589127425b6d5
https://doi.org/10.46563/2686-8997-2022-3-2-96-100
https://doi.org/10.46563/2686-8997-2022-3-2-96-100
Publikováno v:
L.O. Badalyan Neurological Journal. 3:72-81
Chronic inflammatory demyelinating polyneuropathy (CIDP) in children is a rare disease, the genesis of which is autoimmune disorders. In CIDP, autoimmune inflammatory processes are mediated by disorders of both the cellular and humoral links of the i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed9bfd7c91267a140590988153d59e58
https://doi.org/10.46563/2686-8997-2022-3-2-72-81
https://doi.org/10.46563/2686-8997-2022-3-2-72-81
Autor:
Alexey L. Kurenkov, Oleg V. Agranovich, Lyudmila M. Kuzenkova, Lusine G. Khachatryan, Vladimir M. Kenis, Valentina A. Zherebtsova, Marina N. Sarzhina, Niso D. Odinaeva, Ada R. Artemenko, Galina A. Popova, Ekaterina A. Moroshek, Bella I. Bursagova, Vladislav V. Chernikov, Evgeniya E. Tabe, Alexandra A. Nezhelskaya, Anna A. Maksimenko, Leila Ya. Akhadova, Mikhail V. Indereykin, Nina V. Duibanova, Lyudmila V. Tikhonova, Andrey V. Sapogovsky, Zumrut M. Gadzhialieva, Antonina V. Grigorieva, Vladislav S. Perminov, Inessa D. Fedonyuk, Larisa M. Kolpakchi, Yulia A. Kursakova, Natalia A. Tsurina
Publikováno v:
L.O. Badalyan Neurological Journal. 2:189-202
Introduction. In patients with infantile cerebral palsy (CP), botulinum therapy is used to treat both muscle tone disorders and sialorrhea. Therefore, it is logical to use one preparation of botulinum toxin type A to treat spasticity and sialorrhea i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d2a14e3a777354c4f3352fc4b08d492
https://doi.org/10.46563/2686-8997-2021-2-4-189-202
https://doi.org/10.46563/2686-8997-2021-2-4-189-202
Autor:
Lale A. Pak, Svetlana B. Lazurenko, Svetlana B. Makarova, Tatyana V. Sviridova, Lyudmila M. Kuzenkova, Alexey L. Kurenkov, Bella I. Bursagova, Tamara R. Chumbadze
Publikováno v:
L.O. Badalyan Neurological Journal. 2:173-188
Introduction. Currently, Russia does not have a scientifically grounded medical and psychological support system for disabled children (DC), which allows involving them in classes in children and youth schools of adaptive physical education, preparin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::416e9cee8aaad163e3b0239e2f37cae0
https://doi.org/10.46563/2686-8997-2021-2-4-173-188
https://doi.org/10.46563/2686-8997-2021-2-4-173-188