Zobrazeno 1 - 10
of 17
pro vyhledávání: '"L. A. Bessonova"'
Autor:
E. L. Dadali, T. V. Markova, F. M. Bostanova, A. S. Kuchina, L. A. Bessonova, E. A. Melnik, V. V. Zabnenkova, O. P. Ryzhkova, O. E. Agranovich
Publikováno v:
Нервно-мышечные болезни, Vol 14, Iss 1, Pp 42-50 (2024)
A description of the clinical and genetic characteristics of four Russian patients with Schaaf–Yang syndrome, caused by previously described and newly identified nucleotide variants in MAGEL2 gene, is presented. It was shown that the most severe cl
Externí odkaz:
https://doaj.org/article/f7f88af6c86b4e8b84073e720fafedf8
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:
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
Publikováno v:
The EYE GLAZ. 24:15-19
Glaucoma continues to lead among the irreversible causes of blindness and low vision. In some cases, surgical treatment is the method of choice even for newly detected glaucoma. The indication for the use of drains is refractory glaucoma, but today m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::216c493ad539d215c1a69b9b0ac807f7
https://doi.org/10.33791/2222-4408-2022-3-15-19
https://doi.org/10.33791/2222-4408-2022-3-15-19
Autor:
O. A. Staroseltseva, N. V. Nudnov, M. L. Radutnaya, A. N. Kirchin, Е. А. Bondar’, L. V. Bessonova, E. L. Altukhov, A. A. Yakovlev, A. F. Shaybak
Publikováno v:
Вестник рентгенологии и радиологии, Vol 102, Iss 4, Pp 217-226 (2021)
Acute mesenteric ischemia is an acute disruption of blood supply to part of the intestine, which, if untreated, leads to bowel wall necrosis and a patient’s death. Computed tomography (CT) plays a leading role in detecting mesenteric ischemia and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f86f835b3ce07ab3db7ecd6c32fc58b
https://www.russianradiology.ru/jour/article/view/655
https://www.russianradiology.ru/jour/article/view/655
Autor:
V A Kadnikova, O.L. Mironovich, O. P. Ryzhkova, F. A. Konovalov, L. A. Bessonova, S. A. Kurbatov, G. E. Rudenskaya, Peter Sparber
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 121(5)
Objective To estimate the proportion and spectrum of infrequent autosomal dominant spastic paraplegias in a group of families with DNA-confirmed diagnosis and to investigate their molecular and clinical characteristics. Material and methods Ten famil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05e2d09071287ae7eea90187f5f498e8
https://pubmed.ncbi.nlm.nih.gov/34184482
https://pubmed.ncbi.nlm.nih.gov/34184482
Autor:
Therapy», Voronezh, Russia, L. I. Denisenko, E. E. Morozova, V. I. Kotarev, L. P. Bessonova, L. V. Liadova, D. A. Belousov
Publikováno v:
BULLETIN OF VETERINARY PHARMACOLOGY. 2:78-90
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a88e9d3ac1613fca6b1c6bef961e2a4
https://doi.org/10.17238/issn2541-8203.2019.2.78
https://doi.org/10.17238/issn2541-8203.2019.2.78
Autor:
Elena L. Dadali, T. V. Markova, V. A. Kadnikova, A. V. Polyakov, G. E. Rudenskaya, D. N. Khmelkova, D. S. Guseva, L. A. Bessonova, O. P. Ryzhkova
Publikováno v:
BMC Neurology
BMC Neurology, Vol 20, Iss 1, Pp 1-14 (2020)
BMC Neurology, Vol 20, Iss 1, Pp 1-14 (2020)
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 sequencing, SP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5997c481ecc6061f48a1c519e1b357ad
https://doi.org/10.1186/s12883-020-01872-4
https://doi.org/10.1186/s12883-020-01872-4
Publikováno v:
Vestnik Voronežskogo Gosudarstvennogo Universiteta Inženernyh Tehnologij, Vol 0, Iss 1, Pp 143-149 (2015)
The article discusses the new iodine-containing supplements (ID) derived from organic media collagenous animal protein (pork rind, carpatina and collagen) and protein concentrates brands SCANGEN and PROMIL C95. It is shown that the use of these prote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::5184e4835500b8703053aaff09253c4d
https://www.vestnik-vsuet.ru/vguit/article/view/282
https://www.vestnik-vsuet.ru/vguit/article/view/282