Zobrazeno 1 - 10
of 142
pro vyhledávání: '"M S Ignatova"'
Autor:
M S Ignatova
Publikováno v:
Терапевтический архив, Vol 78, Iss 6, Pp 66-73 (2003)
Externí odkaz:
https://doaj.org/article/f388fb6e9ec2407ea00cde4c4bc940d5
Autor:
M. S. Ignatova, N. G. Demenkova
Publikováno v:
Bulletin of the South Ural State University series "Law". 18:737-78
Деменкова Наталья Геннадьевна – кандидат юридических наук, доцент кафедры управления и права, Южно-Уральский государственный универси
Autor:
M. S. Ignatova, V. V. Dlin
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 62, Iss 6, Pp 29-44 (2018)
This literature review is focused to change our ideas about the etiology, pathogenesis and treatment tactics of the nephrotic syndrome in recent decades. The change in the treatment outcomes of the primary nephrotic syndrome in connection with the em
Autor:
V. V. Dlin, M. S. Ignatova
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 61, Iss 6, Pp 21-31 (2017)
Summarized research material for nephropathy associated with the pathology of the complement system in children and adults. Presents clinical, immunological and morphological differences of the nephropathy associated with the pathology of the complem
Autor:
M. S. Ignatova, V. V. Dlin
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 60, Iss 3, Pp 6-9 (2016)
Generalized data on the role of medical genetics in the development of pediatric nephrology are given on the basis of the authors’ observations and modern literature. It is shown that the introduction of genetic researches into the practice of a pe
Autor:
M. S. Ignatova, V. V. Dlin
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 59, Iss 3, Pp 82-90 (2016)
Based on their studies and the data available in the literature, the authors consider current views on hereditary nephropathies running with hematuria, such as Alport syndrome, thin basement membrane disease, C3 glomerulonephritis, etc.).
Publikováno v:
Bulletin of experimental biology and medicine. 159(3)
The parameters characterizing antituberculous immune response at the stage of cytokinedependent activation of T cells were analyzed in 90 patients with pulmonary tuberculosis before etiotropic therapy. Immunophenotyping of T cells for IL-12Rβ2, WSX-
Autor:
M S, Ignatova
Publikováno v:
Vestnik Rossiiskoi akademii meditsinskikh nauk. (11)
The paper describes a number of hereditary nephropathies, including hereditary nephritis (Alport's syndrome), the most common genetically determined renal disease, in the context of recent genetic studies. The specific features of tuberous sclerosis,
Autor:
E S, Moskaleva, O V, Katysheva, E A, Ruzhitskaia, V V, Nevstrueva, E K, Ivanina, M S, Ignatova
Publikováno v:
Terapevticheskii arkhiv. 71(6)
Publikováno v:
Terapevticheskii arkhiv. 69(6)
Investigations performed in the region contaminated with heavy metal salts revealed high prevalence of renal diseases in children. The test for blood polymorphic proteins indicated signs of genetic predisposition to renal damage. Greater occurrence i