Zobrazeno 1 - 10
of 205
pro vyhledávání: '"M. Guseva"'
Autor:
A. F. Murtazina, P. N. Tsabay, G. E. Rudenskaya, L. A. Bessonova, F. M. Bostanova, D. M. Guseva, I. V. Sharkova, O. A. Shchagina, A. A. Orlova, O. P. Ryzhkova, T. V. Markova, A. S. Kuchina, S. S. Nikitin, E. L. Dadali
Publikováno v:
Нервно-мышечные болезни, Vol 13, Iss 2, Pp 42-55 (2023)
TRPV4‑associated neuromuscular diseases represent a clinical spectrum of neuropathies and motor neuron disorders. To date, 3 phenotypic forms are distinguished. There are Charcot–Marie–Tooth disease type 2C, distal hereditary motor neuropathy t
Externí odkaz:
https://doaj.org/article/47a4aae3e5d74c7d8cbc451951a1d757
Publikováno v:
Нервно-мышечные болезни, Vol 11, Iss 1, Pp 19-24 (2021)
Background. Lissencephaly (LIS) is a spectrum of malformations of the cerebral cortex that occur as a result of impaired migration of neuronal precursors to the cortical plate and the formation of furrows and convolutions in the post‑migration peri
Externí odkaz:
https://doaj.org/article/4df255bf4c264de8b16af0b0f9557ea1
Autor:
Konstantin E. Belozerov, Ilia S. Avrusin, Lyubov I. Andaryanova, Anna M. Guseva, Zaira S. Shogenova, Irina N. Belanovich, Anna V. Lobacheva, Tatiana L. Kornishina, Eugenia A. Isupova, Vera V. Masalova, Olga V. Kalashnikova, Andrey V. Nokhrin, Tatyana F. Panova, Yulia P. Dutova, Svetlana L. Myshkovskaya, Kirill Y. Kostyunin, Andrey B. Komissarov, Vyacheslav G. Chasnyk, Liudmila V. Bregel, Mikhail M. Kostik
Publikováno v:
Biomedicines, Vol 11, Iss 3, p 870 (2023)
Background: Several cases of skin and central nervous system vasculopathy associated with COVID-19 in children have been published, but the information is rather limited. Our study aimed to describe these cases of vasculitis associated with COVID-19
Externí odkaz:
https://doaj.org/article/e9d78b0cf04644ebb72d4e6998a0e443
Autor:
D. M. Guseva, E. L. Dadali
Publikováno v:
Нервно-мышечные болезни, Vol 10, Iss 3, Pp 74-79 (2020)
The article describes the clinical and genetic characteristics of 2 patients from Russia with autosomal recessive primary microcephaly type 2, caused by previously described and newly identified mutations in the WDR62 gene. The data obtained the supp
Externí odkaz:
https://doaj.org/article/760a48b15d544fa1a006b0c0ab45f5b8
Publikováno v:
Вестник Самарского университета: История, педагогика, филология, Vol 26, Iss 1, Pp 38-46 (2020)
The article focuses on the study of possibilities of implementing the concept of historical memory, which has been widely used in recent scientific and practical activities. The following tasks contributed to the realization of the intended goal: ana
Externí odkaz:
https://doaj.org/article/c8aac43db8b84fb691e35d5d1f97aad0
Autor:
Galina E. Rudenskaya, Varvara A. Kadnikova, Christian Beetz, Tatyana N. Proskokova, Irina G. Sermyagina, Anna A. Stepanova, Valery P. Fedotov, Elena L. Dadaly, Darya M. Guseva, Тatiana V. Markova, Oksana P. Ryzhkova
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 14, Iss 1, Pp 44-54 (2020)
Introduction. The autosomal dominant hereditary spastic paraplegia type 3 (SPG3), associated with the ATL1 gene, is a common form of the hereditary spastic paraplegia (HSP). The molecular genetic and clinical features of the SPG3 have not been suffic
Externí odkaz:
https://doaj.org/article/cb785b6c298746ea89b96a7bb419e2f1
Autor:
E. I. Dadali, I. A. Akimova, N. A. Semenova, D. M. Guseva, O. A. Shchagina, A. I. Chukhrova, I. V. Kanivets, S. A. Korostelev
Publikováno v:
Нервно-мышечные болезни, Vol 9, Iss 2, Pp 30-36 (2019)
Introduction. The description of the clinical and genetic characteristics of eight patients with autosomal-recessive variant pontocerebellar hypoplasia due to mutations in the TSEN54 gene.Purpose. Description of clinical and genetic characteristics o
Externí odkaz:
https://doaj.org/article/74daf8084a3245bfa34955016f2567f5
Autor:
Tatiana E. Borovik, Maria V. Fomina, Sergey P. Yatsyk, Tatiana V. Bushueva, Natalia G. Zvonkova, Aleksey A. Gusev, Vera A. Skvortsova, Ina Sokolov, Irina M. Guseva, Andrey P. Fisenko, Abdumanap B. Alkhasov
Publikováno v:
Russian Pediatric Journal. 23:82-88
Introduction. To improve the quality of surgical treatment and prevent postoperative complications, there is needed an integrated multidisciplinary professional approach including a combination of nutritional support with therapeutic methods and psyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::899737efa25e86491808775ce5364b71
https://doi.org/10.46563/1560-9561-2023-26-2-82-88
https://doi.org/10.46563/1560-9561-2023-26-2-82-88
Publikováno v:
Information Society. :55-64
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9fa5c7af252b654195f23de92e558426
https://doi.org/10.52605/16059921_2023_01_55
https://doi.org/10.52605/16059921_2023_01_55
Autor:
Tatiana V. Bushueva, Tatiana E. Borovik, Natalya N. Semyonova, Vera A. Skvortsova, Natalia G. Zvonkova, Irina M. Guseva, Elena A. Roslavtseva, Tatyana N. Stepanova, Olga L. Lukoyanova, Anait K. Gevorkyan, Svetlana Т. Bykova, Tamara G. Kalinina
Publikováno v:
Педиатрическая фармакология, Vol 15, Iss 2, Pp 129-134 (2018)
Background. The nutrition of children with phenylketonuria includes specialized starch-based products, the range of which is constantly expanding. Our aim was to study the safety of the composition of starchy flakes enriched with a complex of fat-sol
Externí odkaz:
https://doaj.org/article/129770b0a4c24111b041aec8404ced31