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pro vyhledávání: '"M. Dubko"'
Akademický článek
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Autor:
E. Kalashnikova, R. Raupov, N. Lybimova, E. Kuchinskaya, O. Kalashnikova, V. Chasnyk, T. Kornishina, L. Snegireva, E. Gaidar, V. Masalova, E. Isupova, M. Kaneva, M. Dubko, T. Likhacheva, L. Sorokina, M. Kostik
Publikováno v:
Annals of the Rheumatic Diseases. 81:997.2-997
Backgroundjuvenile systemic lupus erythematosus (jSLE) is the most frequent pediatric connective tissue disease with multiorgan involvement and different outcomes and prognosis. Corticosteroids remain the base treatment option and steroid-sparing tre
Autor:
V. Masalova, Lubov Sorokina, Ilia Avrusin, M. Kostik, T. Likhacheva, I.A. Chikova, M. Gharabaghtsyan, R. Raupov, E. Gaidar, L. Snegireva, S. Khrypov, M. Dubko, N. Garipova, E. Isupova
Publikováno v:
Annals of the Rheumatic Diseases. 80:931-932
Background:Hip osteoarthritis (HOA) is a severe outcome of juvenile idiopathic arthritis (JIA) itself and also can be result of corticosteroid (CS) treatment, if it was used. Total hip arthroplasty (THA) is the last step in JIA treatment and indicate
Autor:
Anastasia V. Tumakova, Ilya V. Bizin, Maria A. Makhova, Lidiya V. Lyazina, Marina N Guseva, Evgeny N. Suspitsin, Mikhail Kostik, Irina Kondratenko, Olga P. Kozlova, Tatiana V. Gabrusskaya, Svetlana S. Vahliarskaya, Anastasia S. Levina, M. Dubko, Olga V. Goleva, Liliya V. Ditkovskaya, Evgeny N. Imyanitov, Nataliya V. Skripchenko, Anna P. Sokolenko, Natalia E. Sokolova
Publikováno v:
Clinical geneticsREFERENCES. 98(3)
Primary immune deficiencies are usually attributed to genetic defects and, therefore, frequently referred to as inborn errors of immunity (IEI). We subjected the genomic DNA of 333 patients with clinical signs of IEI to next generation sequencing (NG
Autor:
I.A. Chikova, M. Dubko, M. Kostik, M. Kaneva, L. Snegireva, T. Likhacheva, T.L. Kornishina, E. Isupova, Vyacheslav Chasnyk, Olga Kalashnikova, V. Masalova, E. Gaidar
Publikováno v:
Annals of the Rheumatic Diseases. 80:937.1-937
Background:Macrophage activation syndrome (MAS) is a severe life-threatening complication of the systemic-onset juvenile idiopathic arthritis (soJIA). The treatment options included high-dose of the corticosteroids (CS), cyclosporine A (CsA), intrave
Autor:
M. Kostik, M. Kaneva, Olga Kalashnikova, M. Dubko, Vyacheslav Chasnyk, E. Isupova, V. Masalova, L. Snegireva, I.A. Chikova, T. Likhacheva, E. Gaidar, M. Chakhalian, T. Nikitina
Publikováno v:
Annals of the Rheumatic Diseases. 80:1402.2-1402
Background:Uveitis is the most common extra-articular manifestation of juvenile idiopathic arthritis (JIA). Usually uveitis developed during first two years after arthritis occurred [1]. In the previous studies was shown the shorter time interval bet
Autor:
R. Raupov, V. Masalova, Evgeny N. Suspitsin, Vyacheslav Chasnyk, Lubov Sorokina, T. Ermachenkova, T. Likhacheva, M. Kostik, Olga Kalashnikova, T. Gabrusskaya, E. Gaidar, M. Dubko, L. Snegireva, E. Isupova, M. Kaneva
Publikováno v:
Annals of the Rheumatic Diseases. 80:247.1-248
Background:While efficacy of tofacitinib (TOF) has been proven in many adult immune-mediated conditions, the information on its’ safety and efficacy in the pediatric population is limited.Objectives:to evaluate the safety and efficacy of TOF in chi
Autor:
Elena D Serogodskaia, V. Masalova, E. Gaidar, Olga Kalashnikova, Anatolii Viktorovich Kononov, Alla Hynes, Liudmila I Grebenkina, Tatiana N. Nikitina, Vyacheslav Chasnyk, Vladimir Keltsev, Tatyana Ammosova, L. Snegireva, Sergei Nekhai, Mikhail Kostik, M. Dubko, Yuri Obukhov, Xionghao Lin
Publikováno v:
Pediatrician (St. Petersburg). 8:5-26
The paper presents epidemiologic and pathophysiological aspects of the problem statement for early recognition of Uveitis (Uv) associated with Juvenile Idiopathic Arthritis (JIA) in terms of the proteomic profile of tears as well as the results of an
Autor:
M. Kostik, Evgeny N. Imyanitov, M. Dubko, Anna P. Sokolenko, A. Yu. Kazantseva, T. Likhacheva, O. V. Kalashnikova, Vyacheslav Chasnyk, E.N. Suspitsyn
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
Autor:
Tatiana Kornishina, V. Masalova, A. Santimov, I.A. Chikova, L. Snegireva, E. Isupova, Tatiana Likhacheva, Maria Rumyantseva, Mikhail Kostik, E. Gaidar, Olga Kalashnikova, M. Dubko
Publikováno v:
Paediatric rheumatology.