Zobrazeno 1 - 10
of 35
pro vyhledávání: '"I. A Tuzankina"'
Autor:
D. A. Cheremokhin, S. S. Deryabina, I. A. Tuzankina, E. V. Vlasova, N. V. Nikitina, M. A. Bolkov
Publikováno v:
Медицинская иммунология, Vol 23, Iss 6, Pp 1357-1366 (2021)
Chromosomal pathology is one of the most common causes of congenital malformations. The CATCH-22 symptom complex is most often associated with a microdeletion of chromosome 22, upon detection of which it is customary to diagnose DiGeorge syndrome, a
Externí odkaz:
https://doaj.org/article/bc5d7ceb87b3484c96b53c29a3c24046
Publikováno v:
Медицинская иммунология, Vol 22, Iss 6, Pp 1163-1172 (2021)
The article presents the results of the work performed by the laboratory of molecular diagnostics at the Medical Center “Health Care of Mother and Child” for the diagnosis of primary immunodeficiency in Sverdlovsk region over 5 years. The laborat
Externí odkaz:
https://doaj.org/article/876fae4f0a3f455fac6ea4eec917acc7
Autor:
I. A. Tuzankina, M. A. Bolkov, N. S. Zhuravleva, Yu. O. Vaseneva, Kh. Shinvari, O. V. Schipacheva
Publikováno v:
Медицинская иммунология, Vol 22, Iss 3, Pp 569-576 (2020)
This article presents two clinical cases of patients with a homozygous deletion of segment of chromosome 1, which covers regions of genes associated with complement factor H, in particular CFHR3. Patients underwent in-depth clinical studies, heredity
Externí odkaz:
https://doaj.org/article/979ddc913ffe41a989d3c485bc7ca3b7
Autor:
N. G. Sarkisian, N. N. Kataeva, I. A. Tuzankina, S. G. Melikyan, V. A. Zurochka, A. V. Zurochka
Publikováno v:
Инфекция и иммунитет, Vol 9, Iss 3-4, Pp 549-558 (2019)
Antibacterial drugs are routinely used in therapy of periodontal diseases. However, increasing incidence of antibiotics resistance necessitates development of novel therapeutic approaches for oral diseases. Currently, newly designed antibacterial age
Externí odkaz:
https://doaj.org/article/8d811d45d83c40139927947a40e1b987
Publikováno v:
Бюллетень сибирской медицины, Vol 18, Iss 3, Pp 144-154 (2019)
To understand the current state of the issue of dental manifestations of primary immunodeficiencies, foreign literature on the problem has been analyzed. The article describes the dental manifestations of many primary immunodeficiencies, which can be
Externí odkaz:
https://doaj.org/article/425f1d38430b4478923221e495dad27c
Publikováno v:
Медицинская иммунология, Vol 20, Iss 1, Pp 85-98 (2018)
As a preparatory stage for implementation of genetic testing for severe combined immunodeficiency under a neonatal screening program, a study was performed in Sverdlovsk Region which concerned quantitative determination of T and B cell neogenesis mar
Externí odkaz:
https://doaj.org/article/29d7a7eeab2b4ac5b4586def680ad857
Publikováno v:
Russian Journal of Immunology. 25:555-560
In the modern world, inborn errors of immunity (IEIs), or primary immunodeficiencies (PIDs), are among of the main causes of childhood disability and mortality, determining the demographic state of mankind not only at present, but also in the future.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be121126322440dde0b88cd520358470
https://doi.org/10.46235/1028-7221-1185-roi
https://doi.org/10.46235/1028-7221-1185-roi
Publikováno v:
Медицинская иммунология, Vol 19, Iss 1, Pp 95-100 (2017)
The work represents a family which includes two siblings with chromosome 22q11.2 deletion syndrome. Their mother carries the same chromosome anomaly, but with apparently normal phenotype. Hence, this interesting case of 22q11.2 deletion syndrome exis
Externí odkaz:
https://doaj.org/article/37f763de45724cc993fe6fdefad04732
Publikováno v:
Медицинская иммунология, Vol 18, Iss 6, Pp 583-588 (2016)
In order to justify a need for mass screening of primary immunodeficiencies (PID) in a regional program for the newborns, we performed a retrospective study of blood spots (archived screening cards) from the babies who deceased at the first year of l
Externí odkaz:
https://doaj.org/article/d6f9db08a1534b2d8d2d2b6935182e0a
Autor:
N. G. Sarkisyan, L. V. Gankovskaya, I. A. Tuzankina, O. A. Svitich, G. I. Ron, V. N. Shershnev, O. N. Kolyadina, M. A. Dolgikh
Publikováno v:
Журнал микробиологии, эпидемиологии и иммунобиологии, Vol 0, Iss 1, Pp 67-71 (2016)
Aim. Search of association of polymorphisms in DEFВ1, IL-10, TNF-a and TLR2 genes with development of chronic generalized periodontitis in representatives of Ural region (Caucasian race). Materials and methods. 142 patients, that were split into 3 g
Externí odkaz:
https://doaj.org/article/671756f13863425fa4616049c84e4a03