Zobrazeno 1 - 10
of 25
pro vyhledávání: '"L M Karzakova"'
Autor:
S. I. Kudryashov, L. M. Karzakova
Publikováno v:
Медицинская иммунология, Vol 26, Iss 4, Pp 853-860 (2024)
One of the urgent problems of medicine is to clarify the pathogenetic mechanisms of glomerulonephritis (GN) with refractory nephrotic syndrome (NS). In 30% of cases, refractory NS has a genetic nature. The role of human histocompatibility system (HLA
Externí odkaz:
https://doaj.org/article/7ad79e35189a4004aa8c1d4cbb00bd11
Publikováno v:
Медицинская иммунология, Vol 26, Iss 1, Pp 181-190 (2024)
Glomerulonephritis (GN) is a group of immuno-inflammatory kidney diseases with predominant glomerular lesions that are difficult to treat. The greatest problems are caused by the treatment of GN with nephrotic syndrome, which often has a recurrent co
Externí odkaz:
https://doaj.org/article/b9bc3e35690f4a99865041bcc4fb45b9
Autor:
L. M. Karzakova, O. M. Muchukova, T. S. Lutkova, S. I. Kudryashov, N. V. Zhuravleva, N. D. Ukhterova, E. S. Gavrilova, I. A. Sidorov, A. V. Odintsova
Publikováno v:
Медицинская иммунология, Vol 23, Iss 2, Pp 353-368 (2021)
In recent years, primary immunodeficiencies have turned from the class of rare diseases to the category of more common disorders which may be encountered by doctors of any clinical discipline. The first case of primary immunodeficiency disorder (PID)
Externí odkaz:
https://doaj.org/article/c07fcf429b68473491edba36dc7df87f
Publikováno v:
Медицинская иммунология, Vol 21, Iss 2, Pp 293-302 (2019)
One of the urgent problems of modern medicine is the search for genetic markers of chronic obstructive pulmonary disease (COPD).The aim of the study was to investigate the relationship between HLA haplotypes and COPD in individuals whose illness deve
Externí odkaz:
https://doaj.org/article/15ed1f362e914c0fa5bffb151fd9c692
Autor:
N A Komelyagina, L M Karzakova, N.V. Zhuravleva, S I Kudryashov, I. A. Sidorov, L V Borisova, A. V. Odintsova
Publikováno v:
Russian Clinical Laboratory Diagnostics. 66:610-617
The timely diagnosis and treatment of post-infectious glomerulonephritis (PIGN) is currently limited by the erased and low-symptom nature of the disease, which leads to the search for informative biological markers of the disease, which can be used a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62bdf3908c3a8b537af1eb65853d237e
https://doi.org/10.51620/0869-2084-2021-66-10-610-617
https://doi.org/10.51620/0869-2084-2021-66-10-610-617
Publikováno v:
Медицинская иммунология, Vol 10, Iss 6, Pp 513-518 (2014)
Abstract. We have examined parameters of innate and adaptive immunity, as well as HLA profile in COPD patients living under the conditions of environmental zinc deficiency (Zn levels in the soil < 0.1 mg/kg, and dietary contents of zinc, 9.1 mg/d, as
Externí odkaz:
https://doaj.org/article/770e386fe1b94abc8113cbff7e45e43c
Publikováno v:
Медицинская иммунология, Vol 7, Iss 1, Pp 57-62 (2014)
Abstract. The purpose of the present investigation was to study the immune status of the patients with acute stroke (54 patients with cerebral infarction; 34 — with cerebral hemorrhage). Evaluation of the immune status included the study of the pop
Externí odkaz:
https://doaj.org/article/5c0c9f8389854eafba28dfff850d1881
Publikováno v:
Медицинская иммунология, Vol 14, Iss 4-5, Pp 433-438 (2014)
Abstract. This work presents immunological data of one-hundred patients with severe pyoinflammatory diseases of face and neck area. Upon laboratory evaluation of patients with such pathology, it was shown that production of IL-1β, IL-2, IL-6, IL-8,
Externí odkaz:
https://doaj.org/article/14211d05ca30429f820becbd358e412a
Publikováno v:
Journal of Bioscience and Applied Research. :45-58
The low effectiveness of the existing ways of treatment of glomerulonephritis (GN) requires the development of new treatment methods and profound studying of mechanisms of development of (GN). A review of modern literature data indicates a relationsh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32206b828d30c426e6d1c72cbbb9e140
https://doi.org/10.21608/jbaar.2021.175196
https://doi.org/10.21608/jbaar.2021.175196
Autor:
N.V. Zhuravleva, N.D. Ukhterova, O. M. Muchukova, Tatyana S. Lutkova, I. A. Sidorov, L M Karzakova, A. V. Odintsova, S I Kudryashov, E. S. Gavrilova
Publikováno v:
Medicinskaâ Immunologiâ, Vol 23, Iss 2, Pp 353-368 (2021)
In recent years, primary immunodeficiencies have turned from the class of rare diseases to the category of more common disorders which may be encountered by doctors of any clinical discipline. The first case of primary immunodeficiency disorder (PID)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4d1529d043cf3c6a4c14d8e9253bd0a
https://doi.org/10.15789/1563-0625-rro-2148
https://doi.org/10.15789/1563-0625-rro-2148