Zobrazeno 1 - 10
of 19
pro vyhledávání: '"M M, Ilkovich"'
Autor:
A. S. Elgouhari, N. M. Lazareva, O. P. Baranova, I. V. Kudryavtsev, T. P. Ses, M. M. Ilkovich, A. A. Totolian
Publikováno v:
Медицинская иммунология, Vol 26, Iss 4, Pp 755-764 (2024)
Sarcoidosis is a multisystem inflammatory disease of unknown etiology characterized by the formation of non-caseating granulomas, most commonly in the lung tissue. It presents with two main forms: acute and chronic. Patients with chronic sarcoidosis
Externí odkaz:
https://doaj.org/article/4a4142217ee4473ca71ccb48220ff35b
Autor:
N. M. Lazareva, I. V. Kudryavtsev, O. P. Baranova, D. V. Isakov, M. K. Serebriakova, A. A. Bazhanov, N. A. Arsentieva, N. E. Liubimova, T. P. Ses’, M. M. Ilkovich, A. A. Totolian
Publikováno v:
Медицинская иммунология, Vol 25, Iss 5, Pp 1049-1058 (2023)
Immune cell hyperactivation along with cytokines they overproduce plays an important role in sarcoidosis and related disease pathogenesis. A central place in the immunopathogenesis of sarcoidosis is held by diverse cell-mediated reactions governed by
Externí odkaz:
https://doaj.org/article/262bf29d573e44e2aef43c438dac5fa2
Autor:
I. V. Kudryavtsev, N. M. Lazareva, O. P. Baranova, M. K. Serebriakova, T. P. Ses’, M. M. Ilkovich, A. A. Totolian
Publikováno v:
Медицинская иммунология, Vol 24, Iss 3, Pp 573-586 (2022)
Sarcoidosis is a multisystemic granulomatous disorder of unknown cause, characterized by formation of immune granulomas in various organs, mainly in lungs. Currently, two main phenotypes of pulmonary sarcoidosis are described, i.e., Lofgren’s syndr
Externí odkaz:
https://doaj.org/article/7e83a774cb6040d2a4f270116a3d1422
Autor:
N. M. Lazareva, O. P. Baranova, I. V. Kudryavtsev, D. V. Isakov, N. A. Arsentieva, N. E. Liubimova, T. P. Ses’, M. M. Ilkovich, A. A. Totolian
Publikováno v:
Медицинская иммунология, Vol 23, Iss 4, Pp 791-798 (2021)
Various immune cells as well as related cytokines are involved in immunopathogenesis of sarcoidosis and mechanisms of granuloma development. Currently, a role for chemokines in sarcoidosis has been extensively investigated, which is paralleled with a
Externí odkaz:
https://doaj.org/article/1210bec412154f91a2e318934f66fd7d
Autor:
N. M. Lazareva, O. P. Baranova, I. V. Kudryavtsev, N. A. Arsentieva, N. E. Liubimova, T. P. Ses’, M. M. Ilkovich, Areg A. Totolian
Publikováno v:
Медицинская иммунология, Vol 23, Iss 1, Pp 73-86 (2021)
Sarcoidosis is a polysystemic inflammatory disease of unknown etiology, morphologically related to the group of granulomatosis, with heterogeneous clinical manifestations and outcomes. Immune cells, in particular T helper cells, are attracted to lung
Externí odkaz:
https://doaj.org/article/0e74c93033564c2f88020c5119001f62
Autor:
N. M. Lazareva, O. P. Baranova, I. V. Kudryavtsev, N. A. Arsentieva, N. E. Liubimova, T. P. Ses’, M. M. Ilkovich, Areg A. Totolian
Publikováno v:
Медицинская иммунология, Vol 22, Iss 5, Pp 993-1002 (2020)
Sarcoidosis is an inflammatory disease of unknown etiology with damage to the lungs and other organs characterized by development of necrosis-free epithelioid cell granulomas. Granulomatous inflammation characterized by the activation of different im
Externí odkaz:
https://doaj.org/article/6cfcf9a2508c4de08ea9ee9ee978d45d
Autor:
N. M. Lazareva, I. V. Kudryavtsev, O. P. Baranova, M. K. Serebriakova, A. A. Bazhanov, T. P. Ses’, M. M. Ilkovich, A. A. Totolian
Publikováno v:
Медицинская иммунология, Vol 21, Iss 6, Pp 1081-1098 (2020)
Sarcoidosis is an inflammatory disease of unknown etiology, characterized by development of necrosis-free epithelioid cell granulomas, resulting in hyperactivation of various cells of the immune system. The role of humoral mechanisms in the pathogene
Externí odkaz:
https://doaj.org/article/8c16232191e74934a684ac5548501266
Autor:
I. V. Kudryavtsev, N. M. Lazareva, O. P. Baranova, A. S. Golovkin, D. V. Isakov, M. K. Serebriakova, T. P. Ses’, M. M. Ilkovich, Areg A. Totolian
Publikováno v:
Медицинская иммунология, Vol 21, Iss 3, Pp 467-478 (2019)
Sarcoidosis is a disorder of unknown etiology characterized by development of necrosis-free epithelioid cell granulomas in various tissues. There are two main phenotypes of pulmonary sarcoidosis (PS): Lofgren’s syndrome (LS) is an acute form with f
Externí odkaz:
https://doaj.org/article/6b7c030954df40b3ba1281b68c28aa24
Autor:
A. G. Chuchalin, S. N. Avdeev, Z. R. Aisanov, O. P. Baranova, S. E. Borisov, N. A. Geppe, A. A. Vizel’, I. Yu. Vizel’, A. A. Zaicev, N. Y. Kravchenko, M. M. Ilkovich, O. V. Lovacheva, A. B. Malakhov, A. G. Malyavin, D. V. Petrov, V. V. Romanov, I. V. Sivokozov, M. V. Samsonova, I. P. Solovieva, I. E. Stepanyan, S. A. Terpigorev, I. E. Tyurin, L. Ya. Frantsuzevich, A. L. Chernyaev, E. I. Shmelev, N. M. Shmeleva
Publikováno v:
PULMONOLOGIYA. 32:806-833
Sarcoidosis is a multi-organ granulomatosis of unknown origin. Modern diagnostic methods allow detecting this disease at an early stage. The absence of specific markers requires a comprehensive approach to diagnosis based on comparison of radiation,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5210feb4dfa986661430684e0b8db30
https://doi.org/10.18093/0869-0189-2022-32-6-806-833
https://doi.org/10.18093/0869-0189-2022-32-6-806-833
Autor:
S. N. Avdeev, Z. R. Aisanov, A. S. Belevskiy, M. M. Ilkovich, E. A. Kogan, Z. M. Merzhoeva, D. V. Petrov, M. V. Samsonova, S. A. Terpigorev, N. V. Trushenko, I. N. Trofimenko, I. E. Tyurin, A. L. Chernyaev, B. A. Chernyak, A. V. Chernyak, S. Yu. Chikina, A. G. Chuchalin, E. I. Shmelev
Publikováno v:
PULMONOLOGIYA. 32:473-495
Idiopathic pulmonary fibrosis (IPF) is a specific form of chronic fibrotic interstitial pneumonia with a progressive course and poor prognosis. The prevalence of IPF in the Russian Federation is about 8 – 12 cases per 100,000 population. The basic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::caf8a53a6bb4fdb71a1604d2445a3714
https://doi.org/10.18093/0869-0189-2022-32-3-473-495
https://doi.org/10.18093/0869-0189-2022-32-3-473-495