Zobrazeno 1 - 10
of 15
pro vyhledávání: '"S I, Polyakova"'
Autor:
I E Khatkov, I V Maev, D S Bordin, Yu A Kucheryavyi, S R Abdulkhakov, S A Alekseenko, E I Alieva, R B Alikhanov, I G Bakulin, A Yu Baranovsky, E V Beloborodova, E A Belousova, I M Buriev, E V Bystrovskaya, S V Vertyankin, L V Vinokurova, E I Galperin, A V Gorelov, V B Grinevich, M V Danilov, V V Darvin, E A Dubtsova, T G Dyuzheva, V I Egorov, M G Efanov, N V Zakharova, V E Zagainov, V T Ivashkin, R E Izrailov, N V Korochanskaya, E A Kornienko, V L Korobka, N Yu Kokhanenko, M A Livzan, I D Loranskaya, K A Nikolskaya, M F Osipenko, A V Okhlobystin, V D Pasechnikov, E Yu Plotnikova, S I Polyakova, O A Sablin, V I Simanenkov, N I Ursova, V V Tsvirkun, V V Tsukanov, A V Shabunin
Publikováno v:
Терапевтический архив, Vol 89, Iss 8, Pp 80-87 (2017)
Pancreatology Club Professional Medical Community, 1A.S. Loginov Moscow Clinical Research and Practical Center, Moscow Healthcare Department, Moscow; 2A.I. Evdokimov Moscow State University of Medicine and Dentistry, Ministry of Health of Russia, Mos
Externí odkaz:
https://doaj.org/article/403b6fc4ca824cb1b125e8ef15c66b8a
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:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 66, Iss 5, Pp 233-239 (2021)
Mucopolysaccharidosis (MPS) type III (Sanfilippo syndrome) is a lysosomal storage disease inherited in an autosomal recessive manner, it is characterized by the accumulation of heparan sulfate in the cells of the body, which leads to the development
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70055e99941b714f668b4fe46f2e2a9f
https://doi.org/10.21508/1027-4065-2021-66-5-233-239
https://doi.org/10.21508/1027-4065-2021-66-5-233-239
Publikováno v:
Российский журнал гастроэнтерологии, гепатологии, колопроктологии, Vol 25, Iss 6, Pp 25-30 (2015)
Aim of investigation. To carry out objective estimation of liver parenchyma state in children with the 1-st type hereditary tyrosinemia (НТ-1) by ultrasound method with quantitative estimation of hepatic parenchyma pattern.Material and methods. Ove
Externí odkaz:
https://doaj.org/article/e5fc519db3ca456da0e0b92ac0ebaf31
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 66, Iss 4, Pp 16-24 (2021)
The review presents data on the biological significance of plasmalogens, their synthesis in peroxisomes, subsequent transformation cascade, and the relevance of their role in the pathogenesis of a number of diseases. Plasmalogens, being a unique subc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::584a2d171019b47bba3d9948f2e5b6fc
https://doi.org/10.21508/1027-4065-2021-66-4-16-24
https://doi.org/10.21508/1027-4065-2021-66-4-16-24
Publikováno v:
Journal of Ophthalmology, Iss 1, Pp 77-79 (2016)
Externí odkaz:
https://doaj.org/article/0065c2cfe75c4e8aa5ed1a3bb9bc4568
Publikováno v:
Педиатрическая фармакология, Vol 11, Iss 4, Pp 116-119 (2014)
The article is dedicated to a pressing issue of pediatrics — diagnosis and treatment of an autosomal-recessive disease from the group of organic acidemias — methylmalonic acidemia. Despite the attained progress in diagnosis of this disease based
Externí odkaz:
https://doaj.org/article/3af3ebe419344f48969afacd3ae3bb78
Autor:
G. V. Volynets, A. S. Potapov, S. I. Polyakova, A. E. Aleksandrov, V. M. Senyakovich, A. N. Surkov, T. S. Chetkina, N. N. Evlukhina, T. A. Skvortsova
Publikováno v:
Вопросы современной педиатрии, Vol 12, Iss 4, Pp 47-51 (2013)
Aim: to develop a system of evaluation of liver failure stage in children based on the International classification of functioning, disability and health (ICF). Patients and methods: based on the retrospective analysis of 14 biochemical markers, char
Externí odkaz:
https://doaj.org/article/75858145de6048679fbb4920c1dcaeaa
Autor:
S I Polyakova
Publikováno v:
Аутизм и нарушение развития, Vol 17, Iss 1, Pp 55-70 (2019)
A metabolic disorder is a serious problem. Changes that occur at the cellular level and are associated with biochemical processes lead to malfunctioning of the cell, and further, respectively, of tissue, organ, of the whole organism. Metabolic care i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9313676c7de734fc30a53725dd3ac613
http://psyjournals.ru/files/97714/autdd_2019_n1_polyakova.pdf
http://psyjournals.ru/files/97714/autdd_2019_n1_polyakova.pdf
Autor:
Dmitry S. Bordin, E A Kornienko, E. V. Bystrovskaya, N Yu Kokhanenko, N.I. Ursova, T G Dyuzheva, Igor Khatkov, V. D. Pasechnikov, Igor G. Bakulin, Maria A. Livzan, Emilia Galperin, N. V. Korochanskaya, E V Beloborodova, E.I. Alieva, A. V. Okhlobystin, S I Polyakova, V L Korobka, Sayar Abdulkhakov, S V Vertyankin, Oleg A. Sablin, M F Osipenko, I D Loranskaya, Yu A Kucheryavyi, E. A. Belousova, A Yu Baranovsky, V V Tsukanov, V E Zagainov, Mikhail Efanov, Roman Izrailov, A.V. Gorelov, E Yu Plotnikova, V I Egorov, E.A. Dubtsova, V I Simanenkov, Zakharova Nv, R B Alikhanov, K.A. Nikolskaya, Victor Tsvirkun, Vladimir Ivashkin, A V Shabunin, Grinevich Vb, S A Alekseenko, V V Darvin, M V Danilov, L V Vinokurova, I M Buriev, Igor V. Maev
Publikováno v:
Терапевтический архив, Vol 89, Iss 8, Pp 80-87 (2017)
SCOPUS00403660-2017-89-8-SID85030449492
SCOPUS00403660-2017-89-8-SID85030449492
Pancreatology Club Professional Medical Community, 1A.S. Loginov Moscow Clinical Research and Practical Center, Moscow Healthcare Department, Moscow; 2A.I. Evdokimov Moscow State University of Medicine and Dentistry, Ministry of Health of Russia, Mos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3183813b783dfa6d0b413f33a92edf13
https://ter-arkhiv.ru/0040-3660/article/viewFile/32316/pdf
https://ter-arkhiv.ru/0040-3660/article/viewFile/32316/pdf