Zobrazeno 1 - 10
of 24
pro vyhledávání: '"N. Shapovalenko"'
Publikováno v:
Український антарктичний журнал, Iss 2, Pp 94-105 (2021)
The immune system plays a major role in human homeostasis, yet a body’s unique individuality complicates the diagnostic forecasting of unfavourable physiological states and diseases. Studying the immunophenotypic features of winterers of the Ukrain
Externí odkaz:
https://doaj.org/article/e552381294854c0db868b3d152712b56
Autor:
Е. S. Fedorov, S. О. Salugina, Е. Yu. Zakharova, А. N. Shapovalenko, S. G. Radenska-Lopovok, V. G. Matkava, А. N. Arefieva
Publikováno v:
Научно-практическая ревматология, Vol 62, Iss 2, Pp 216-226 (2024)
Monogenic familial autoinflammatory Behçet-like syndrome/haploinsufficiency A20 syndrome is a hereditary autoinflammatory disease from the group of ubiquitinopathies which are caused by a mutation of the TNFAIP3 gene encoding the A20 protein with an
Externí odkaz:
https://doaj.org/article/1be9774c6e3a4c9199cd1dc478df9a9c
Publikováno v:
Научно-практическая ревматология, Vol 62, Iss 4 (2024)
The treatment of systemic lupus erythematosus with juvenile onset (jSLE) remains a difficult task, taking into account the more aggressive course of the disease, requiring the appointment of various therapy regimens, including mainly a combination of
Externí odkaz:
https://doaj.org/article/230206639b104356b9d6a2e962bbfcaf
Autor:
M. I. Kaleda, I. P. Nikishina, A. N. Latypova, N. N. Yudkina, Zh. G. Verizhnikova, A. N. Shapovalenko, T. N. Pachkoria
Publikováno v:
Современная ревматология, Vol 18, Iss 1, Pp 62-69 (2024)
Mixed connective tissue disease (MCTD) is one of the very rare systemic autoimmune diseases; it accounts for 0.1–0.6% of cases in pediatric rheumatologists' practices. MCTD is characterized by a broad spectrum of clinical manifestations and a high
Externí odkaz:
https://doaj.org/article/dd0561bcecdf44409426cbc0f9f74857
Autor:
M. I. Kaleda, I. P. Nikishina, S. O. Salugina, E. S. Fedorov, S. V. Arsenyeva, A. N. Shapovalenko, T. N. Pachkoria, V. G. Matkava
Publikováno v:
Современная ревматология, Vol 16, Iss 4, Pp 32-39 (2022)
Juvenile idiopathic inflammatory myopathies (JIIM) are rare diseases in which the prognosis is largely determined by timely diagnosis, timing of prescription and effectiveness of therapy.Objective: to characterize the clinical phenotypes, the results
Externí odkaz:
https://doaj.org/article/802559bbc4eb4aa98dd723665e3e0220
Autor:
M. I. Kaleda, I. P. Nikishina, E. V. Nikolaeva, A. N. Shapovalenko, E. S. Fedorov, T. N. Pachkoria
Publikováno v:
Научно-практическая ревматология, Vol 59, Iss 2, Pp 208-214 (2021)
Objective: to analyze the safety of rituximab (RTM) in children with various rheumatic diseases.Materials and methods. The retrospective study included 81 pediatric patients with a confirmed diagnosis of rheumatic disease. Data on the safety of RTM w
Externí odkaz:
https://doaj.org/article/2651932c642a4d9ba309aaf0eaad7829
Publikováno v:
Научно-практическая ревматология, Vol 55, Iss 6, Pp 662-667 (2018)
Tocilizumab (TCZ) is one of the biological agents that are most commonly used in the treatment of juvenile idiopathic arthritis (JIA), especially its systemic variant. The development of neutropenia, which is associated with the use of TCZ and its me
Externí odkaz:
https://doaj.org/article/d0059567bfd04f8590e705d3b3ac3daa
Publikováno v:
Современная ревматология, Vol 15, Iss 1, Pp 20-26 (2021)
Seropositive juvenile rheumatoid arthritis (JRA) is the rarest subtype of juvenile idiopathic arthritis (JIA) that is the equivalent of RA in adults and is manifested mainly by a symmetric polyarticular lesion, rapid structural disease progression wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fab50858b671d4b593a8122c216f8352
https://mrj.ima-press.net/mrj/article/view/1095
https://mrj.ima-press.net/mrj/article/view/1095
Publikováno v:
Научно-практическая ревматология, Vol 45, Iss 5, Pp 74-82 (2007)
Externí odkaz:
https://doaj.org/article/a7a7313fe6b847d89946b57f48977028
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