Zobrazeno 1 - 10
of 38
pro vyhledávání: '"V. I. Larionova"'
Autor:
S. I. MELNIK, M. V. PINEVSKAYA, E. A. ORLOVA, S. V. STAREVSKAYA, I. Y. MELNIKOVA, V. I. LARIONOVA
Publikováno v:
Медицинский совет, Vol 0, Iss 9, Pp 166-170 (2017)
Hereditary deficiency of the alpha-1-antitrypsin occupies a leading position among the causes of chronic nonspecific lung diseases with emphysema formation. Deficiency of alpha-1-antitrypsin is a potentially fatal hereditary disease, under-diagnosed
Externí odkaz:
https://doaj.org/article/27f70a79081f4ce4903fa262180520b0
Autor:
S. S. Nikitin, S. I. Kutsev, E. N. Basargina, S. V. Mikhaylova, E. Yu. Zakharova, V. I. Larionova, S. I. Polyakova, N. P. Kotlukova, E. N. Arkhipova, M. O. Kovalchuk, N. V. Buchinskaya
Publikováno v:
Нервно-мышечные болезни, Vol 6, Iss 1, Pp 11-43 (2016)
Externí odkaz:
https://doaj.org/article/e0cae3a787574e14abdbd6b1dc15e6db
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 4, Iss 1, Pp 33-38 (2016)
Aim. To study association between stroke and gene polymorphism of angeotensin converting enzyme (ACE), angeotensin II type 1 receptor (ATR1), apolipoprotein СIII (APO CIII), apoproteine Е (APO E), methylentetrahydrofolate reductase (MTHFR), fibrino
Externí odkaz:
https://doaj.org/article/386114231fa14205b0fd47b51777b29c
Publikováno v:
Современная ревматология, Vol 8, Iss 3, Pp 28-33 (2014)
Juvenile idiopathic arthritis (JIA) is a chronic inflammatory joint disease associated with impaired immune system performance. The specific features of JIA may be genetically determined.Objective: to assess JIA activity in children with vitamin D re
Externí odkaz:
https://doaj.org/article/012da262d7db4a6bb0c650e1c29a4fe3
Publikováno v:
Педиатрическая фармакология, Vol 9, Iss 3, Pp 52-57 (2012)
We investigated the polymorphism of the gene p53 exon 4 Arg72Pro and intron 3 ins/del 16 b. p. in children with juvenile idiopathic arthritis in order to identify the influence of gene polymorphisms on the course and outcome of the disease. The child
Externí odkaz:
https://doaj.org/article/6b5d1754c7544693bbdbc6abaa8615b0
Autor:
M. M. KOSTIK, M. M. MNUSKINA, I N MAKAROVA, D. A. KUZ'MINA, L. A. ShchEPLYaGINA, V. I. LARIONOVA
Publikováno v:
Остеопороз и остеопатии, Vol 14, Iss 3, Pp 19-23 (2011)
This study describes bone metabolism in children withjuvenile idiopathic arthritis (JIA), association between disturbances of bone metabolism with inflammatory activity, juvenile arthritis disease course and therapy in 198 children. Low bone mineral
Externí odkaz:
https://doaj.org/article/9a89787932b14fce9cb7a81eaa98ee1a
Publikováno v:
Abstracts.
Introduction Chronic gastroduodenitis in adolescents is often accompanied by a decrease in bone density. The mechanisms of this relationship are not fully understood. Objective To study the level of 25 (OH)-vitamin D, vitamin D receptor gene polymorp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c72b1b42c35955cdcc0b63f0c1124822
https://doi.org/10.1136/archdischild-2019-epa.206
https://doi.org/10.1136/archdischild-2019-epa.206
Publikováno v:
Остеопороз и остеопатии, Vol 17, Iss 2, Pp 11-15 (2014)
The aim of this study was to assess the role of simple clinical and laboratorial markers for prediction of low bone mineral density (LBMD < -2 SD) in children with juvenile idiopathic arthritis (JIA). Low weight and linear growth ( 5.0, DAS > 2.9, DA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab024f0409d05fb67ad208dfa2716471
https://endojournals.ru/index.php/osteo/article/view/8881
https://endojournals.ru/index.php/osteo/article/view/8881
Autor:
H. .. An-Hahar, V. I. Larionova, Olga Belyaeva, O. Berkovich, Elena Baranova, O. O. Bolsha-Kova
Publikováno v:
"Arterial’naya Gipertenziya" ("Arterial Hypertension"). 18:255-266
Objective. To evaluate G-75A and C+83T polymorphisms of apolipoprotein A1 gene and Q192R polymorphism of paraoxonase 1 gene and their association with blood pressure and lipid levels in patients with abdominal obesity. Design and methods. We examined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79e5f8f4e19c8e0492cd45300e4fa2b8
https://doi.org/10.18705/1607-419x-2012-18-3-255-266
https://doi.org/10.18705/1607-419x-2012-18-3-255-266
Autor:
V S Tikhonova, A N Voytovich, A V Kamaev, T E Ivashchenko, A V Orlov, L A Zhelenina, D S Korostovtsev, V I Larionova, A N Voitovich, T E Ivaschenko, D S Korostovsev
Publikováno v:
Russian Journal of Allergy. 8:24-27
Background. To detect sixteen cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations most common to Russian populations in children with severe asthma (SA). Patients and Methods. S A group included 59 children aged 4-17 years old (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8ece28d89cbe9070f01f9a145376abf
https://doi.org/10.36691/rja783
https://doi.org/10.36691/rja783