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:
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://doaj.org/article/cd563438ddb1438c85c3383a41b59250
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:
Научно-практическая ревматология, Vol 45, Iss 3, Pp 90-95 (2007)
Bone mineral density (BMD), bone biochemical markers, influence of inflammation and glucocorticoid administration on bone metabolism in 70 children with chronic arthritis were studied. Osteopenia was detected by dual energetic X-ray absorptiometry L1
Externí odkaz:
https://doaj.org/article/72b3e9c9f7664a4b84429f99431f9be6
Autor:
O N Semenova, M M Kostik, S I Yagashkina, M A Bogdanova, A N Voytovich, O S Romashkina, L A Shcheplyagina, V I Larionova
Publikováno v:
Остеопороз и остеопатии, Vol 14, Iss 2, Pp 11-13 (2011)
The aim of our study is researching influence of vitamin D and osteocalcin polymorphic gene markers in people, who lived in Blockaded Leningrad in 1941-1944 and detecting “critical age” of peak bone mass formation in these people. We included in
Externí odkaz:
https://doaj.org/article/0032b8088a454e4f9db77981f060ac25
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