Zobrazeno 1 - 10
of 31
pro vyhledávání: '"V. G. Chasnyk"'
Publikováno v:
Обозрение психиатрии и медицинской психологии имени В.М. Бехтерева, Vol 0, Iss 4-2, Pp 78-86 (2020)
In order to study the effect of anxiety and depression on the severity of chronic pain syndrome, 216 patients with the diagnosis of juvenile idiopathic arthritis (JIA) were examined. All children included in the study underwent a traditional rheumato
Externí odkaz:
https://doaj.org/article/62b0d94e49e443ffabbd09c6eb54114d
Autor:
M. M. Kostik, E. A. Isupova, I. A. Chikova, M. F. Dubko, V. V. Masalova, L. S. Snegireva, O. V. Kalashnikova, V. G. Chasnyk
Publikováno v:
Современная ревматология, Vol 11, Iss 4, Pp 30-39 (2018)
Objective: to study the efficiency and safety of tocilizumab (TCZ) therapy in patients with systemic-onset juvenile idiopathic arthritis (sJIA). Patients and methods. The retrospective study included 48 children with active sJIA in whom TCZ therapy w
Externí odkaz:
https://doaj.org/article/bf5b12068cc44ba7b021aee4e1f349b5
Autor:
A. V. Santimov, R. A. Rupp, I. G. Alekseev, N. N. Plutova, E. A. Moskvina, M. K. Kruchina, A. N. Tarasenko, N. E. Sokolova, E. A. Savelyeva, I. Yu. Bogdanov, D. V. Ivanov, T. I. Kandrina, O. V. Kopanevich, A. Ya. Grafskaya, N. A. Ignatyeva, D. B. Pulukchu, N. V. Pavlova, I. V. Solodkova, O. V. Kalashnikova, T. L. Kornishina, M. F. Dubko, V. G. Chasnyk, M. M. Kostik
Publikováno v:
Современная ревматология, Vol 11, Iss 3, Pp 26-32 (2017)
Kawasaki disease (KD) is acute systemic vasculitis of unknown etiology. Approximately 20–25% of untreated patients develop coronary artery changes with a range of severity from asymptomatic coronary artery dilatation to giant coronary artery aneury
Externí odkaz:
https://doaj.org/article/da8a3c8c1f3342c5b2fe172a90d9c178
Autor:
M. F. Dubko, E. N. Suspitsyn, A. P. Sokolenko, E. N. Imyanitov, T. S. Likhacheva, A. Yu. Kazantseva, O. V. Kalashnikova, V. G. Chasnyk, M. M. Kostik
Publikováno v:
Современная ревматология, Vol 11, Iss 2, Pp 41-46 (2017)
Autoinflammatory diseases (AIDs) are a group of rare disorders characterized by persistent or recurrent inflammation caused by the hyperactivation of mediators and innate immune cells (neutrophils, monocytes/macrophages). The paper describes the auth
Externí odkaz:
https://doaj.org/article/34711b88ab69439c8db9e3f8ba5d9e19
Autor:
E. V. Gaidar, M. M. Kostik, M. F. Dubko, V. V. Masalova, L. S. Snegireva, E. A. Isupova, T. N. Nikitina, E. D. Serogodskaya, O. V. Kalashnikova, V. G. Chasnyk
Publikováno v:
Педиатрическая фармакология, Vol 13, Iss 4, Pp 340-344 (2016)
Background: Juvenile idiopathic arthritis (JIA) associated uveitis may be the cause of not only visual acuity decrement, but also blindness. At the same time, in some patients therapy with methotrexate can not prevent the development of these complic
Externí odkaz:
https://doaj.org/article/f97cc0bd41274ac085ce2ba372bf2e82
Autor:
M. Yu. Rykov, I. V. Filinov, E. I. Petrov, N. D. Vashakmadze, A. K. Gevorkyan, E. N. Arkhipova, I. V. Sil’nova, E. N. Basargina, N. V. Buchinskaya, A. I. Ivanov, E. A. Isupova, M. M. Kostik, N. A. Abramova, O. V. Kalashnikova, V. G. Chasnyk, A. E. Aleksandrov, D. A. Morozov, V. G. Polyakov
Publikováno v:
Вопросы современной педиатрии, Vol 14, Iss 4, Pp 522-527 (2015)
Many orphan diseases in children require life-long and regular intravenous enzyme replacement therapy. The article describes the first Russian practice of implanting venous port systems in 12 patients with type I and II mucopolysaccharidosis and Pomp
Externí odkaz:
https://doaj.org/article/30fb0bcb0fcd4f17b6b03dd25e321218
Autor:
M. M. Kostik, E. V. Gaydar, M. F. Dubko, V. V. Masalova, L. S. Snegireva, I. A. Chikova, E. A. Isupova, T. N. Nikitina, E. D. Serogodskaya, O. V. Kalashnikova, A. Ravelli, V. G. Chasnyk
Publikováno v:
Вопросы современной педиатрии, Vol 14, Iss 4, Pp 477-482 (2015)
Background: Uveitis is one of the most common extra-articular manifestations of juvenile idiopathic arthritis (JIA). Currently, the possibility of reducing the risk of uveitis in children with JIA by using methotrexate has been studied.Objective: Our
Externí odkaz:
https://doaj.org/article/9bc2729b6f294ef38331519246db5ed7
Autor:
I. A. Chikova, M. M. Kostik, E. V. Sinelnikova, M. F. Dubko, O. I. Krasnogorskaya, A. I. Imelbaev, R. N. Polozov, N. V. Buchinskaya, E. A. Isupova, E. V. Gaidar, O. V. Kalashnikova, R. A. Nasyrov, V. G. Chasnyk
Publikováno v:
Научно-практическая ревматология, Vol 53, Iss 3, Pp 319-322 (2015)
Pachydermodactyly is a rare form of fibromatosis, which is characterized by an asymptomatic soft tissue enlargement around the proximal interphalangeal (PIP) joints of the hand. The etiology of the disease is unknown. Its possible triggers are recurr
Externí odkaz:
https://doaj.org/article/d99d1c5fa07e4eafac1280d98068148f
Autor:
M. M. Kostik, M. F. Dubko, V. V. Masalova, L. S. Snegireva, I. A. Chikova, E. A. Isupova, O. V. Kalashnikova, V. G. Chasnyk
Publikováno v:
Современная ревматология, Vol 9, Iss 1, Pp 55-59 (2015)
Macrophage activation syndrome (MAS) is a severe life-threatening complication presenting with hemophagocytosis, pancytopenia, coagulopathy, and liver and CNS dysfunctions. The disease belongs to a group of histiocytic disorders. The common triggers
Externí odkaz:
https://doaj.org/article/f083e23c209a48a8806adb12dc87a5c8
Autor:
I. A. Chikova, N. V. Buchinskaya, М. М. Kostik, V. V. Avramenko, O. L. Krasnogorskaya, R. A. Nasirov, T. Levade, V. G. Chasnyk
Publikováno v:
Вопросы современной педиатрии, Vol 13, Iss 6, Pp 78-84 (2014)
Farber disease (lipogranulomatosis, OMIM 228000) — is extremely rare autosomal-recessive disorder from group of lysosomal storage disorders, due to deficiency of acid ceramidase activity enzyme. Farber disease has a lot of clinical masques and rese
Externí odkaz:
https://doaj.org/article/d1aaa2f995ec4645a49fc0c164681ebd