Zobrazeno 1 - 10
of 28
pro vyhledávání: '"K V Savost'yanov"'
Autor:
T. V. Sleptsova, E. I. Alexeeva, K. V. Savost’yanov, A. A. Pushkov, T. M. Bzarova, S. I. Valieva, O. L. Lomakina, R. V. Denisova, K. B. Isaeva, E. G. Chistyakova
Publikováno v:
Педиатрическая фармакология, Vol 13, Iss 2, Pp 143-148 (2016)
The article shows the observation of rare NLPC4-associated autoinflammatory syndrome with enterocolitis and familial cold urticaria. Diagnosis is confirmed molecularly-genetically: previously not described mutation c.928C>T in the heterozygous state
Externí odkaz:
https://doaj.org/article/02d2b0c5e3464d21b2c28ffab04d2102
Publikováno v:
Нервно-мышечные болезни, Vol 6, Iss 1, Pp 54-62 (2016)
Pompe disease (PD) is a rare, progressive, commonly fatal inherited autosomal recessive disease that is difficult to diagnose due to its obvious clinical heterogeneity and low awareness among physicians. Access to the laboratory diagnosis of rare dis
Externí odkaz:
https://doaj.org/article/4620dd8cb8204649bdd61accdbaf8881
Autor:
I. S. Kostushina, T. V. Margieva, T. N. Gusarova, G. T. Yakhyaeva, L. S. Namazova-Baranova, A. A. Pushkov, K. V. Savost'yanov
Publikováno v:
Педиатрическая фармакология, Vol 11, Iss 6, Pp 62-65 (2014)
Nephrotic syndrome is a severe renal disease that may result in the end-stage renal failure despite the extent of proteinuria. Prognosis and tactics of therapy of nephrotic syndrome depend both on the morphological diagnosis and on the cause of the d
Externí odkaz:
https://doaj.org/article/f48e1be13f6c4414be8954e941cc35ef
Autor:
T. V. Sleptsova, E. I. Alexeeva, K. V. Savost’yanov, A. A. Pushkov, A. G. Nikitin, T. M. Bzarova, S. I. Valieva, A. N. Fetisova, A. V. Pakhomov, N. V. Zhurkova, R. V. Denisova, K. B. Isaeva, E. G. Chistyakova
Publikováno v:
Вопросы современной педиатрии, Vol 13, Iss 3, Pp 97-103 (2014)
The article describes the monitoring of severe cryopyrin-associated syndrome (syndrome CINCA/NOMID). The following clinical case indicates successful application of homogeneous antibodies to interleukin 1 — canakinumab — in patient with chronic n
Externí odkaz:
https://doaj.org/article/c4e2f6cb60724f079bcaac6c72e71609
Autor:
Valery Vyacheslavovich Nosikov, Yu A Seregin, Elena Vital'evna Titovich, K V Savost'yanov, Lyubov' Iosifovna Zil'berman, D A Chistyakov, Tamara Leonidovna Kuraeva, Ivan Ivanovich Dedov
Publikováno v:
Сахарный диабет, Vol 5, Iss 1, Pp 34-37 (2002)
Цель: изучение сцепления с СД типа 1 ряда полиморфных маркеров, расположенных в локусах IDDM8, IDDM9, IDDM10 и IDDM12, с использованием семей с конкор
Externí odkaz:
https://doaj.org/article/a13cd95a61064f7b9da8521b01af8e6c
Autor:
Timofey Alexandrovich Chistyakov, K V Savost'yanov, R I Turakulov, L N Shcherbacheva, Galina Grigor'evna Mamaeva, Mikhail Ivanovich Balabolkin, Valery Vyacheslavovich Nosikov, Ivan Ivanovich Dedov
Publikováno v:
Сахарный диабет, Vol 3, Iss 3, Pp 2-7 (2000)
Актуальность Повышенное содержание глюкозы в крови при сахарном диабете (СД) способствует развитию окислительного стресса, выражающег
Externí odkaz:
https://doaj.org/article/72013511a9f14c89b2c7215c246fa51d
Autor:
A Chernysheva, Lyubov' Iosifovna Zil'berman, K V Savost'yanov, N M Tsitlidze, Tamara Leonidovna Kuraeva, Valentina Alexandrovna Peterkova, Ivan Ivanovich Dedov, Valery Vyacheslavovich Nosikov
Publikováno v:
Сахарный диабет, Vol 10, Iss 2, Pp 6-8 (2007)
Цель. Исследовать возможное влияние локуса IDDM18 на предрасположенность к СД1 в семьях из русской популяции. Материалы и методы. Исследова
Externí odkaz:
https://doaj.org/article/c20f11c1308f466aa66caa2d35994b32
Autor:
K V Savost'yanov, Timofey Alexandrovich Chistyakov, Marina Vladimirovna Shestakova, O E Voron'ko, L D Chugunova, Minara Shamkhalovna Shamkhalova, Ivan Ivanovich Dedov, Valery Vyacheslavovich Nosikov
Publikováno v:
Сахарный диабет, Vol 5, Iss 3, Pp 2-4 (2002)
Термин диабетическая нефропатия (ДН) относится к ?поздним? микрососудистым осложнениям диабета, которые развиваются спустя годы проявл
Externí odkaz:
https://doaj.org/article/c7f27fc3344941cf864c19975b790299
Publikováno v:
Nervno-Myšečnye Bolezni, Vol 6, Iss 1, Pp 54-62 (2016)
Pompe disease (PD) is a rare, progressive, commonly fatal inherited autosomal recessive disease that is difficult to diagnose due to its obvious clinical heterogeneity and low awareness among physicians. Access to the laboratory diagnosis of rare dis
Autor:
A N, Surkov, L S, Namazova-Baranova, A S, Potapov, K V, Savost'yanov, A A, Pushkov, A G, Nikitin, S I, Polyakova, M V, Ryazanov, O V, Kustova, V I, Barskii, M Yu, Stepanyan
Publikováno v:
Vestnik Rossiiskoi akademii meditsinskikh nauk. (11-12)
We represented a case history of multiple hepatic adenomas in an adolescent with severe clinical course of glycogen storage disease type lb (compound heterozygous mutations c.1042_1043delCT and c.817GA in the SLC37A4). The patient was prescribed a ra