Zobrazeno 1 - 10
of 32
pro vyhledávání: '"P E, Povilaitite"'
Publikováno v:
Успехи молекулярной онкологии, Vol 9, Iss 4 (2022)
Introduction. Disturbances in the PI3K-dependent (PI3K – phosphoinositide 3‑kinase) cascade are characteristic of all types of breast cancer. In particular, 30–40 % of patients with advanced / metastatic hormone-positive HER2‑negative (HER2
Externí odkaz:
https://doaj.org/article/3d690671f0bc436ea95028bbb08ad99e
Publikováno v:
Сибирский научный медицинский журнал, Vol 39, Iss 5, Pp 134-140 (2019)
The defining feature of HER2/neu-positive Luminal B and HER2/neu-positive (non-luminal) subtype breast cancer is HER2/neu gene amplification and protein overexpression on cancer cell membrane. The HER2-targeted therapy is nowadays available for patie
Externí odkaz:
https://doaj.org/article/3743e35c9f824e09b347b1c85ea23740
Publikováno v:
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 67:75-82
The authors analyzed clinical and morphological correlations between the manifestations and outcome in nephritis with Henoch– Schönlein purpura and assessed the effect of morphological data on achieving remission as per ISKDC, SQC, MEST-C classifi
Publikováno v:
Nephrology (Saint-Petersburg). 26:74-79
BACKGROUND. The widespread use of genetic methods in clinical practice has shown that pathogenic variants in COL4A3, COL4A4, COL4A5 genes associated with Alport syndrome (AS) are detected in 10 % of sporadic and in 20 % of familial cases of IgA nephr
Autor:
E. S. Rusakova, E. K. Petrosyan, M. S. Molchanova, V. A. Gavrilova, A. V. Ryzhova, B. L. Kushnir, P. E. Povilaitite, P. V. Shumilov
Publikováno v:
Nephrology (Saint-Petersburg). 26:80-87
BACKGROUND. Steroid-dependent nephrotic syndrome (SDNS) treatment is still an important problem in pediatric nephrology since the proper use of steroid-sparing agents can reduce the frequency of relapses and avoid steroid toxicity. THE AIM of our stu
Publikováno v:
Терапевтический архив, Vol 88, Iss 6, Pp 80-83 (2016)
The paper describes a clinical case of a female woman with nephropathy due to light chain deposition disease caused by secretion of κ Bence-Jones protein. Complete immunochemical remission was achieved after induction therapy using a bortezomib + cy
Externí odkaz:
https://doaj.org/article/4b5f2aa401c5438b9dcae0f85cba3d9f
Publikováno v:
Nephrology (Saint-Petersburg). 25:48-56
BACKGROUND. The course and outcomes of primary IgA nephropathy in children are variable. Early therapy for high-risk individuals can help to delay the development of end-stage renal disease.THE AIM: to analysis of risk factors for progression and out
Publikováno v:
Nephrology (Saint-Petersburg). 25:73-78
IgG4-related disease (IgG4-AD), is a fibro-inflammatory condition characterized by an increase of serum IgG4 and infiltration of the tissue of affected organs by IgG4-positive plasma cells. There is a significant cross between IgG4-AB and antineutrop
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 65, Iss 6, Pp 42-49 (2021)
The Alport’s syndrome is the hereditary multisystem disease characterized by the development of the progressive nephropathy. The early diagnosis and subsequent prescription of nephroprotective therapy improves significantly the nephrological progno
Publikováno v:
Вестник урологии, Vol 0, Iss 3, Pp 30-38 (2013)
The article describes the clinical observation of toxic chronic tubulointerstitial nephritis due to prolonged use of herbal drug Agrimonia Eupatoria. The toxic effects of A.Eupatoria more associated not with specific toxicants, and the presence of a
Externí odkaz:
https://doaj.org/article/7a9265d8bfd147e088b4e69a196990c2