Zobrazeno 1 - 10
of 12
pro vyhledávání: '"E K Petrosyan"'
Publikováno v:
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 68:22-28
Idiopathic nephrotic syndrome is the most common glomerular disease in children, with a prevalence of 1.15–16.9 cases per 100,000 children per year worldwide. In some cases, nephrotic syndrome has a frequently relapsing course or dependence on ster
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). 26:66-73
BACKGROUND: Alport syndrome is a non-immune genetically determined glomerulopathy caused by mutation of genes encoding α3-5 chains of collagen type IV of the basement membranes. It manifests with hematuria and/or proteinuria, progressive renal funct
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
Autor:
М. I. Dubrovskaya, А. S. Botkina, N. V. Davidenko, T. V. Zubova, V. B. Lyalikova, K. V. Shebalkina, E. K. Petrosyan
Publikováno v:
Вопросы современной педиатрии, Vol 14, Iss 3, Pp 402-407 (2015)
The article focuses on the development of malabsorption syndrome in young children suffering food allergies and protein-losing enteropathy resulting from failure to follow contemporary nutrition principles. The clinical events demonstrate the consequ
Externí odkaz:
https://doaj.org/article/c74ace4115664e4d8c4f19266cddb3a3
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
Autor:
E. K. Petrosyan
Publikováno v:
Social'naja politika i social'noe partnerstvo (Social Policy and Social Partnership). :135-138
Anti-crisis PR is usually the most difficult area of public relations. The issues of practical anti-crisis PR are related to the theoretical and methodological problems that exist in this area. This article discusses attempts at anti-crisis managemen
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
Autor:
E.V. Pushkareva, P. E. Povilaitite, E. K. Petrosyan, P.V. Shumilov, B. L. Kushnir, Rostov Region pataloanatomical Bureau
Publikováno v:
Nephrology and dialysis. 20:324-238
Publikováno v:
Russian Journal of Genetics. 43:196-199
A comparative analysis of allele and genotype distribution of polymorphic markers Val762Ala and Leu54Phe of ADPRT1 gene encoding poly(ADP-ribose)polymerase1 has been performed in chronic glomerulonephritis patients compared to normal controls. This h