Zobrazeno 1 - 10
of 48
pro vyhledávání: '"D A, 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:
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
Autor:
G. E. Rudenskaya, V. A. Kadnikova, O. P. Ryzhkova, L. A. Bessonova, E. L. Dadali, D. S. Guseva, T. V. Markova, D. N. Khmelkova, A. V. Polyakov
Publikováno v:
BMC Neurology, Vol 20, Iss 1, Pp 1-14 (2020)
Abstract Background Spastic paraplegia type 30 (SPG30) caused by KIF1A mutations was first reported in 2011 and was initially considered a very rare autosomal recessive (AR) form. In the last years, thanks to the development of massive parallel seque
Externí odkaz:
https://doaj.org/article/7e59f0dee73549889e88ab69b144c29c
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
Publikováno v:
Polymer Reviews. :1-39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f70051fd4827361db7b33b32f9a749d8
https://doi.org/10.1080/15583724.2023.2174136
https://doi.org/10.1080/15583724.2023.2174136
Autor:
D. A. Guseva
Publikováno v:
Bulletin of the Moscow State Regional University (Economics). :52-57
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3908e8934959e2c35d40029a1c61ec4f
https://doi.org/10.18384/2310-6646-2022-3-52-57
https://doi.org/10.18384/2310-6646-2022-3-52-57
Publikováno v:
Doklady Physical Chemistry. 500:92-96
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::138c6c8deaea18668f6e92a089680741
https://doi.org/10.1134/s0012501621090025
https://doi.org/10.1134/s0012501621090025
Publikováno v:
Детские инфекции (Москва), Vol 12, Iss 3, Pp 36-39 (2015)
A clinical and laboratory surveillance of 59 children with purulent bacterial meningitis (PBM) of various etiologies was carried out. Of them 29 children received Viferon® at dosages according to the age. Viferon was prescribed in addition to basic
Externí odkaz:
https://doaj.org/article/7884487a550c49139dfb3f3ff7e7c6c3
Autor:
D. A. Guseva, E. S Podbornova
Publikováno v:
EKONOMIKA I UPRAVLENIE: PROBLEMY, RESHENIYA. 1:24-28
This article defines the functions, concepts and condition of insurance services and the market of insurance services in the Russian Federation, as well as types of insurance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3fb5fbe7bcd91709ea99fd919c583227
https://doi.org/10.36871/ek.up.p.r.2020.08.01.003
https://doi.org/10.36871/ek.up.p.r.2020.08.01.003