Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Belyashova AS"'
Autor:
Andrey Marakhonov, Anna Mukhina, Elena Vlasova, Irina Efimova, Natalya Balinova, Yulia Rodina, Dmitry Pershin, Zhanna Markova, Marina Minzhenkova, Nadezhda Shilova, Dzhaina Mudaeva, Djamila Saydaeva, Taisiya Irbaieva, Svetlana Matulevich, Elena Belyashova, Grigoriy Yakubovskiy, Inna Tebieva, Yulia Gabisova, Murat Ikaev, Nataliya Irinina, Liya Nurgalieva, Elena Saifullina, Tatiana Belyaeva, Olga Romanova, Sergey Voronin, Rena Zinchenko, Anna Shcherbina, Sergey Kutsev
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Newborn screening (NBS) for severe combined immunodeficiency (SCID) has been widely implemented to enable early detection and intervention. Trisomy 21, commonly known as Down syndrome (DS), poses unique challenges in NBS due to its frequent associati
Externí odkaz:
https://doaj.org/article/5dfc78da418c415dbb00aa1672da4957
Autor:
Efimova, Irina Yu., Zinchenko, Rena A., Marakhonov, Andrey V., Balinova, Natalya V., Mikhalchuk, Kristina A., Shchagina, Olga A., Polyakov, Alexander V., Mudaeva, Dzhaina A., Saydaeva, Djamila H., Matulevich, Svetlana A., Parshintseva, Polina D., Belyashova, Elena Yu., Yakubovskiy, Grigoriy I., Tebieva, Inna S., Gabisova, Yulia V., Irinina, Nataliya A., Jamschikova, Anna V., Nurgalieva, Liya R., Saifullina, Elena V., Nevmerzhitskaya, Kristina S., Belyaeva, Tatiana I., Romanova, Olga S., Voronin, Sergey V., Kutsev, Sergey I.
Publikováno v:
In Pediatric Neurology July 2024 156:147-154
Akademický článek
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Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
S. V. Mikhailova, E. V. Saifullina, P. V. Baranova, V. P. Vorontsova, D. I. Gribov, M. V. Zhivihina, A. N. Slatetskaya, R. V. Magzhanov, V. A. Samokhvalov, M. N. Virtseva, L. P. Borscheva, E. E. Koh, M. V. Novikova, A. V. Abrukova, E. Yu. Belyashova, N. Yu. Gerasimenko, L. V. Guseva, Zh. V. Yukhimenko, N. V. Nikitina, T. I. Belyaeva, T. A. Shkurko, N. A. Pichkur, V. S. Kakaulina, N. L. Pechatnikova, N . A. Polyakova, S. A. Korostelev, D. V. Pyankov, I. V. Kanivets, N. A. Demina, E. Yu. Pyrkova, G. V. Baidakova, M. V. Kurkina, E. Yu. Zakharova
Publikováno v:
Нервно-мышечные болезни, Vol 11, Iss 2, Pp 61-79 (2021)
Background. Glutaric aciduria type 1 is an autosomal recessive disease caused by mutations in the GCDH gene, which encodes the enzyme glutaryl‑CoA dehydrogenase. Metabolic crisis in type 1 glutaric aciduria is an acute life‑threatening condition
Externí odkaz:
https://doaj.org/article/7260ea8a4de74abc9f7f0ad19298c84e
Autor:
Galina Pavlova, Alexandra Belyashova, Ekaterina Savchenko, Dmitri Panteleev, Dzhirgala Shamadykova, Anna Nikolaeva, Svetlana Pavlova, Alexander Revishchin, Denis Golbin, Alexander Potapov, Natalia Antipina, Andrey Golanov
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
Radiation therapy induces double-stranded DNA breaks in tumor cells, which leads to their death. A fraction of glioblastoma cells repair such breaks and reinitiate tumor growth. It was necessary to identify the relationship between high radiation dos
Externí odkaz:
https://doaj.org/article/7ef7ab58fac146b8934f26e7e7595a53
Publikováno v:
Changing Societies & Personalities, Vol 5, Iss 1, Pp 63-82 (2021)
The article shows the results of a study aimed at finding the determinants, which describe the petitioning activity of the residents of the western and eastern parts of Germany. The research material consists of 1,036 petitions from the German-langua
Externí odkaz:
https://doaj.org/article/af92003052484bdab7634d530e5b56f7
Autor:
N.A. Semenova, G.V. Baydakova, N.V. Nikitina, V.K. Podolina, E.Yu. Belyashova, V.N. Kuznetsova, E.M. Kochegurova, L.P. Andreeva, O.N. Khaylova, S.I. Kutsev
Publikováno v:
РМЖ. Мать и дитя, Vol 2, Iss 4 (2019)
N.A. Semenova1, G.V. Baydakova1, N.V. Nikitina2, V.K. Podolina2, E.Yu. Belyashova3, V.N. Kuznetsova3, E.M. Kochegurova4, L.P. Andreeva5, O.N. Khaylova5, S.I. Kutsev1 1Research Centre for Medical Genetics, Moscow, Russian Federation 2Clinical an
Externí odkaz:
https://doaj.org/article/af540f7141204b9a9c3ca3a2c817bcb0
Autor:
A.S. Belyashova Belyashova, Yu Yu Trunin, E.A. Kobyakova Kobyakova, N.G. Kobyakov Kobyakov, A Yu Belyaev, K.S. Lodygina Lodygina, O.V. Absalyamova Absalyamova, D Yu Usachev, G.L. Kobyakov Kobyakov
Publikováno v:
Pharmateca. :21-33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af53cb710f9dfd319a1659451b3954f1
https://doi.org/10.18565/pharmateca.2021.11.21-33
https://doi.org/10.18565/pharmateca.2021.11.21-33
Autor:
M. A. Belyashova, D. Yu. Ovsyannikov
Publikováno v:
Педиатрическая фармакология, Vol 11, Iss 6, Pp 56-61 (2014)
Brain-lung-thyroid syndrome is a rare genetic disease characterized by pathology of the syndrome affected organs. This syndrome is based on mutations of the NKX2-1 gene, which encodes the thyroid transcription factor. Clinical manifestation of brain-
Externí odkaz:
https://doaj.org/article/d73e731a30e649018f3f8c2fc9977443