Zobrazeno 1 - 10
of 22
pro vyhledávání: '"K V Savost'yanov"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ed09518b35e2024b9380461e96760a6
https://doi.org/10.17650/2222-8721-2016-6-1-54-62
https://doi.org/10.17650/2222-8721-2016-6-1-54-62
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:
Pediatričeskaâ Farmakologiâ, 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://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf5e7e6d042792da2131938bd291e8c8
https://doi.org/10.15690/pf.v13i2.1555
https://doi.org/10.15690/pf.v13i2.1555
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:
Pediatričeskaâ Farmakologiâ, 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://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fcce884c1ae851281f0a336c3f31544
https://doi.org/10.15690/pf.v11i6.1217
https://doi.org/10.15690/pf.v11i6.1217
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::32defe4e4838437bd914364d80c7f0d7
https://pubmed.ncbi.nlm.nih.gov/25971127
https://pubmed.ncbi.nlm.nih.gov/25971127
Autor:
N. Yu. Yakunina, Marina Vladimirovna Shestakova, Olga K. Vikulova, K V Savost'yanov, Ivan Ivanovich Dedov, Chugunova La, M Sh Shamkhalova, Nosikov Vv, O. E. Voron’ko
Publikováno v:
Russian Journal of Genetics. 41:760-765
In groups of type 1 diabetes mellitus patients with and without clinical signs of diabetic nephropathy (n = 62 and 68, respectively), a search was made for associations between diabetic nephropathy and the polymorphic marker e2/e3/e4 of apolipoprotei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::838149d47bf701aa1e9d8a0cfdcd31c0
https://doi.org/10.1007/s11177-005-0157-y
https://doi.org/10.1007/s11177-005-0157-y
Autor:
D. A. Chistyakov, Tamara Leonidovna Kuraeva, Elena Vital'evna Titovich, L. I. Zilberman, Valery V. Nosikov, K V Savost'yanov, Ivan Ivanovich Dedov, Yu. A. Seregin
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::c77662691c9fa50713c362a3d433daca
https://www.dia-endojournals.ru/jour/article/view/5851
https://www.dia-endojournals.ru/jour/article/view/5851