Zobrazeno 1 - 10
of 112
pro vyhledávání: '"T V Beketova"'
Autor:
V V Kraeva, T V Beketova
Publikováno v:
Терапевтический архив, Vol 91, Iss 5, Pp 76-83 (2019)
In the article, we report the causes of pulmonary hemorrhage (PH) according to the literature data and own experience, with an emphasis on patients suffering from rheumatic diseases. Methods of diagnosis and modern approaches to the treatment of PH a
Externí odkaz:
https://doaj.org/article/ffd4d0c4e3434a55a001ae091685b4c2
Autor:
T V Beketova
Publikováno v:
Терапевтический архив, Vol 90, Iss 5, Pp 13-21 (2018)
Antineutrophil cytoplasm antibody (ANCA)-associated vasculitis (AAV) are rare autoimmune disorders and characterized by severe multiple organ lesions with a potential fatal outcome. AAV comprises granulomatosis with polyangiitis (GPA), microscopic po
Externí odkaz:
https://doaj.org/article/7ad322b26ac9454abaa0ad98b1097f42
Autor:
T M Ignatova, L V Kozlovskaya, N B Gordovskaya, O A Chernova, S Yu Milovanova, P I Novikov, T P Nekrasova, T V Beketova, N A Mukhin
Publikováno v:
Терапевтический архив, Vol 89, Iss 5, Pp 46-52 (2017)
Aim. To summarize the experience of a multidisciplinary therapy hospital in treating patients with hepatitis C virus (HCV)-associated cryoglobulinemic vasculitis (CV). Subjects and methods. Seventy-two patients (mean age, 49.4±10.3 years) with HCV-a
Externí odkaz:
https://doaj.org/article/5fcafc2d5c674a3eaf7e43e17d6da874
Publikováno v:
Терапевтический архив, Vol 88, Iss 5, Pp 86-92 (2016)
The 2015 international guidelines for the diagnosis and treatment of eosinophilic granulomatosis with polyangiitis, formerly known as the Churg-Strauss syndrome, are detailed and an attempt is made to expand an evidence base, by attracting more recen
Externí odkaz:
https://doaj.org/article/c7c0fc744d544a4b84b744706141c261
Autor:
T V Beketova
Publikováno v:
Терапевтический архив, Vol 87, Iss 5, Pp 33-46 (2015)
Aim. To study the clinical features of early- and extended-stage microscopic polyangiitis (MPA) and its outcomes on the basis of a long-term follow-up in a rheumatologist’s practice. Subjects and methods. The clinical features of early- and extende
Externí odkaz:
https://doaj.org/article/57f4dce6286346a8ac6eeed225c8fad5
Autor:
T V Beketova
Publikováno v:
Терапевтический архив, Vol 86, Iss 5, Pp 94-98 (2014)
Systemic vasculitides (SV) are severe multiorgan diseases whose early diagnosis and treatment can significantly improve prognosis. Improving the classification of SV may lead to a significant reduction in the likelihood of diagnostic errors. The pres
Externí odkaz:
https://doaj.org/article/7f1fd1747ee44ca1aa83a1e72c8f5ad4
Autor:
T V Beketova, E L Nasonov
Publikováno v:
Терапевтический архив, Vol 84, Iss 5, Pp 68-74 (2012)
Systemic vasculitis (SV) pathogenetically associated with anti-neutrophilic cytoplasmic antibodies (ANCA) is the subject of intensive research in present-day rheumatology. There were noticeable changes in ANCA-associated SV (ANCA-SV) nomenclature in
Externí odkaz:
https://doaj.org/article/514a25e0299347989d1e27770027510e
Publikováno v:
Терапевтический архив, Vol 80, Iss 12, Pp 69-73 (2008)
Externí odkaz:
https://doaj.org/article/95a327f908164948b7cb15e87dd91b77
Publikováno v:
Терапевтический архив, Vol 79, Iss 5, Pp 22-28 (2004)
Aim. To investigate occurrence and diagnostic significance of antibodies to proteinase-3 (aPR-3) and myeloperoxidase (aMPO) in systemic vasculitis (SV). Material and methods. A total of 98 patients with different forms of SV were examined: nonspecifi
Externí odkaz:
https://doaj.org/article/0df4609772ca4a3eaf91e88ce91890da
Autor:
T. V. Beketova
Publikováno v:
Научно-практическая ревматология, Vol 61, Iss 5, Pp 531-536 (2023)
The new 2022 classification criteria for antineutrophil cytoplasmic antibodies associated vasculitis (AAV), proposed by the American College of Rheumatology (ACR) and the European Alliance of Associations for Rheumatology (EULAR), was an important st
Externí odkaz:
https://doaj.org/article/bfae3ac9ce954c4dbf353072dcfd9bee