Zobrazeno 1 - 10
of 25
pro vyhledávání: '"nephrobiopsy"'
Publikováno v:
Вестник Витебского государственного медицинского университета, Vol 22, Iss 2, Pp 35-46 (2023)
Lupus nephritis is characterized by a variety of clinical and morphological manifestations. Histological changes in the renal tissue often determine the course and prognosis of the disease. The performance of nephrobiopsy provides an important inform
Externí odkaz:
https://doaj.org/article/8f3378a609a841c7963136bfcbfc972c
Publikováno v:
Počki, Vol 11, Iss 1, Pp 45-52 (2022)
Proliferative glomerulonephritis (GN) with monoclonal immunoglobulin deposits (PGNMIDs) is a recently described entity among the spectrum of monoclonal gammopathy of renal significance (MGRS). The disease is renal limited and manifests in chronic glo
Externí odkaz:
https://doaj.org/article/a5b28c2e9e744a5593598662a72c6c43
Autor:
N. V. Fomina, E. V. Utkina
Publikováno v:
Архивъ внутренней медицины, Vol 11, Iss 5, Pp 325-334 (2021)
The article discusses the concept of monoclonal renal gammopathy, which combines various renal diseases caused by the deposition of monoclonal immunoglobulin and / or their components in the glomeruli and tubulointerstitium. This nosological group wa
Externí odkaz:
https://doaj.org/article/db086dcfb0e74683bb7d7208f017e487
Publikováno v:
Počki, Vol 10, Iss 2, Pp 70-77 (2021)
There is a complex bidirectional relationship between rheumatic diseases and cancer. Certain rheumatic diseases, in particular dermatomyositis, polymyositis, rheumatoid arthritis, systemic lupus erythematosus, Sjogren’s syndrome, and systemic scler
Externí odkaz:
https://doaj.org/article/ab795f58d4ce44bc86d4bcddc9f69ecd
Publikováno v:
Klinicist, Vol 12, Iss 2, Pp 37-42 (2018)
The aim of study was to describe a clinical case of a hereditary disease with autosomal recessive type of inheritance – familial Mediterranean fever (FMF).Materials and methods. Patient A., 19 years old, Armenian, was hospitalized in the Department
Externí odkaz:
https://doaj.org/article/1523c20a3c964085af8bc54a0b0cfda8
Autor:
I.Yu. Golovach, Ye.D. Yehudina
Publikováno v:
Počki, Vol 7, Iss 4, Pp 298-310 (2018)
Scleroderma renal crisis (SRC) is a major complication in patients with systemic sclerosis. SRC occurs in about 5–25 % of all patients with scleroderma. It is characterized by malignant hypertension and olig-/anuric acute renal failure. Around 10 %
Externí odkaz:
https://doaj.org/article/80140b4f19d6467ca50d9c0b91d27ede
Autor:
T. G. Shekhovtseva, M. A. Dolinna
Publikováno v:
Український Журнал Нефрології та Діалізу, Iss 1(61) (2019)
Abstract. According to current presentations, primary AL-amyloidosis (AL-A) and multiple myeloma, associated and not associated with AL-A, are considered as a part of uniform β-lymphocytic dislocation that is characterized by proliferation of abnorm
Externí odkaz:
https://doaj.org/article/faf28d2f7fa14aa7a2bba398c2678109
Введение: трансплантация почки, обеспечивающая высокое качество жизни пациентам с терминальной хронической почечной недостаточностью
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::505ac05455d7d529d21e94d3fd278703
Publikováno v:
Počki, Vol 10, Iss 2, Pp 70-77 (2021)
KIDNEYS; Vol. 10 No. 2 (2021); 70-77
Почки-Počki; Том 10 № 2 (2021); 70-77
Нирки-Počki; Том 10 № 2 (2021); 70-77
KIDNEYS; Vol. 10 No. 2 (2021); 70-77
Почки-Počki; Том 10 № 2 (2021); 70-77
Нирки-Počki; Том 10 № 2 (2021); 70-77
There is a complex bidirectional relationship between rheumatic diseases and cancer. Certain rheumatic diseases, in particular dermatomyositis, polymyositis, rheumatoid arthritis, systemic lupus erythematosus, Sjogren’s syndrome, and systemic scler
Autor:
I.Yu. Golovach, Ye.D. Yehudina
Publikováno v:
KIDNEYS; Том 7, № 4 (2018); 298-310
Почки-Počki; Том 7, № 4 (2018); 298-310
Нирки-Počki; Том 7, № 4 (2018); 298-310
Почки-Počki; Том 7, № 4 (2018); 298-310
Нирки-Počki; Том 7, № 4 (2018); 298-310
Scleroderma renal crisis (SRC) is a major complication in patients with systemic sclerosis. SRC occurs in about 5–25 % of all patients with scleroderma. It is characterized by malignant hypertension and olig-/anuric acute renal failure. Around 10 %