Zobrazeno 1 - 10
of 60
pro vyhledávání: '"N V Kokosadze"'
Autor:
V. I. Vasiliev, V. R. Gorodetskiy, B. D. Chaltsev, N. A. Probatova, N. S. Shornikova, N. V. Kokosadze, A. I. Pavlovskaya, E. A. Borisenko, I. V. Gaiduk
Publikováno v:
Современная ревматология, Vol 16, Iss 6, Pp 84-91 (2022)
This article describes a case of a transformed diffuse large B-cell lymphoma of the stomach in a patient with Sjögren's disease (SjD) and systemic sclerosis (SSc), as well as a brief review of the literature on lymphoproliferative diseases in SjD an
Externí odkaz:
https://doaj.org/article/4bd13a9bba464c02aaf0e865164ba075
Autor:
V. i. Vasiljev, N. A. Probatova, N. N. Tupitsyn, E. Y. Varlamova, O. A. Logvinenko, A. M. Kovrigina, E. M. Sholohova, M. V. Simonova, T. N. Safonova, V. R. Gorodetsky, N. V. Kokosadze, A. M. Pavlovskaya, T. N. Kondratjeva, Z. G. Kadagidze, E. V. Gayduk
Publikováno v:
Онкогематология, Vol 0, Iss 3, Pp 16-26 (2022)
During long term follow up (median 10 years) of 412 patients with primary Sjogren's syndrome (pSS) 46; (11,2%) women developed non-Hodgkin's lymphoma (NHL). Median pSS duration before development of NHL was 17 years. 43 (93,3%) patients had B-cell an
Externí odkaz:
https://doaj.org/article/8a947f2af17e42a58b1c3ea1e6aded5b
Autor:
V. I. Vasil'ev, B. D. Chal'tsev, V. R. Gorodetskii, S. G. Pal'shina, N. S. Shornikova, L. P. Anan'eva, I. V. Gaiduk, N. V. Kokosadze, N. A. Probatova, A. I. Pavlovskaia, E. B. Rodionova, T. N. Safonova, A. A. Balabina
Publikováno v:
Терапевтический архив, Vol 92, Iss 12, Pp 126-136 (2020)
Despite the large number of studies devoted to the study of systemic sclerosis (SSc), the high risk of developing lymphomas in this disease, the relationship of their development with certain subtypes of SSc and specific SSc-associated autoantibodies
Externí odkaz:
https://doaj.org/article/fdeb9b88367d40e3a26c6fd203470653
Autor:
T. V. Beketova, N. V. Kokosadze
Publikováno v:
Научно-практическая ревматология, Vol 58, Iss 5, Pp 550-559 (2020)
Systemic vasculitis (SV) associated with anti-neutrophilic cytoplasmic antibodies is a multifactorial process characterized by the variability of the epitope specificity of anti-neutrophilic cytoplasmic antibodies and the diversity of clinical phenot
Externí odkaz:
https://doaj.org/article/dbc172619faa43efab430c0ba2207422
Autor:
V. I. Vasilyev, S. G. Palshina, A. I. Pavlovskaya, N. V. Kokosadze, B. D. Chaltsev, L. A. Shornikova
Publikováno v:
Терапевтический архив, Vol 92, Iss 5, Pp 78-84 (2020)
Idiopathic multicentric Castlemans disease is a rare lymphoproliferative disorder that has many similar laboratory, radiological, clinical and pathological manifestations with various conditions, including IgG4-related disease. Increased activity of
Externí odkaz:
https://doaj.org/article/1d51dd40f7914121a68a134a20cdcace
Publikováno v:
Современная ревматология, Vol 14, Iss 1, Pp 74-77 (2020)
IgG4-related disease (IgG4-RD) is a rare immune-mediated fibroinflammatory disease that is characterized by the occurrence of nodules in one or more organs and proceeds in most patients with the elevated levels of IgG4 in serum and/or in the tissues
Externí odkaz:
https://doaj.org/article/0a5c2f7bc6cb4b2d945623df29c5e5b2
Autor:
V. Е. Bugaev, M. P. Nikulin, N. I. Pospekhova, V. M. Safronova, N. V. Kokosadze, Ya. A. Bozhchenko, S. N. Nered, L. N. Lyubchenko, I. S. Stilidi
Publikováno v:
Успехи молекулярной онкологии, Vol 6, Iss 3, Pp 37-48 (2019)
Background. Leiomyosarcoma is one of the most common types of soft tissue sarcomas. Radical surgical resection with subsequent adjuvant chemotherapy remain the most effective treatment approach. Immunotherapy based on inhibition of PD-L1 (programmed
Externí odkaz:
https://doaj.org/article/fea2f4fb439949de87b671113b8b70b6
Autor:
E V Sokol, V I Vasilyev, S G Palshina, N V Kokosadze, N A Probatova, A M Kovrigina, T N Safonova, E B Rodionova, I V Gaiduk, E I Selifanova
Publikováno v:
Терапевтический архив, Vol 91, Iss 5, Pp 40-48 (2019)
Aim: to propose diagnostic algorithm of IgG4-related disease (IgG4-RD). Materials and methods. One center retrospective research. 52 pts with IgG4-RD were included. The diagnosis was proved histologically and immunohistochemically. 48 out of 52 pts r
Externí odkaz:
https://doaj.org/article/aea07e5fadd747bcbfd55d7249309150
Autor:
V. I. Vasilyev, I. V. Gaiduk, S. G. Palshina, V. R. Gorodetsky, E. V. Sokol, E. B. Rodionova, M. V. Burtseva, N. S. Shornikova, N. A. Probatova, N. V. Kokosadze, A. I. Pavlovskaya, N. A. Kupryshina, T. N. Safonova
Publikováno v:
Современная ревматология, Vol 13, Iss 1, Pp 44-51 (2019)
Objective: to identify the main types of lymphoma with the onset of involvement of the major salivary glands (MSGs), which are encountered in rheumatologic practice, and to evaluate the efficiency of minimally invasive incisional biopsies of the MSGs
Externí odkaz:
https://doaj.org/article/c7b06a86d3364f728de57bda55452af8
Autor:
V I Vasilyev, T N Safonova, E V Socol, N A Probatova, N V Kokosadze, A I Pavlovskaya, A M Kovrigina, S G Radenska-Lopovok, V R Gorodetsky, E B Rodionova, S G Palshina, E N Aleksandrova, N S Shornikova, I V Gaiduk
Publikováno v:
Терапевтический архив, Vol 90, Iss 5, Pp 61-71 (2018)
Purpose of the study. To provide demographic, clinical, laboratory, ultrasound, radiological, morphological/ immunomorphological phenotype of IgG4-related ophthalmic diseases, which allowsmaking a differential diagnosis with granulomatous, autoimmune
Externí odkaz:
https://doaj.org/article/5f4d5a2178b24246b17eff4b48fb8113