Zobrazeno 1 - 10
of 80
pro vyhledávání: '"E A, Erokhina"'
Autor:
A. G. Klementieva, E. K. Erokhina, K. V. Shamtieva, E. A. Melnik, A. N. Khrobostova, M. B. Filipenko, A. A. Arakelyants, T. V. Peters, E. P. Pavlikova
Publikováno v:
Кардиоваскулярная терапия и профилактика, Vol 23, Iss 8 (2024)
Aim. To characterize cardiac damage in myotonic dystrophy type 1 (MD1), which is the most common form of hereditary primary muscular pathology in adults.Material and methods. Forty-eight patients with MD1 (31 men, 17 women, mean age 39,2±9,3 years)
Externí odkaz:
https://doaj.org/article/4f118968596a4566aa139a72c24b653c
Autor:
E. V. Erokhina
Publikováno v:
Вестник Российского экономического университета имени Г. В. Плеханова, Vol 0, Iss 2, Pp 94-101 (2024)
The article deals with problems connected with monetary and credit policy of the Russian Federation in new economic and geo-political conditions, such as mass sanction pressure on home economy, serious fluctuations of raw material prices, drastic cha
Externí odkaz:
https://doaj.org/article/c8b256b657bc4543a77357a38e63b3f1
Autor:
E. K. Erokhina, K. V. Shamtieva, E. A. Melnik, D. O. Kazakov, S. A. Kurbatov, E. P. Pavlikova, O. A. Tikhonova, E. A. Mershina, V. E. Sinitsyn, D. V. Vlodavets
Publikováno v:
Нервно-мышечные болезни, Vol 14, Iss 2 (2024)
Background. Myotonic dystrophy type 1 (DM1) is a hereditary slowly progressive multisystem disease with an autosomal dominant mode of inheritance, caused by the expansion of trinucleotide (CTG)n repeats in the 3’ untranslated region of the DMPK gen
Externí odkaz:
https://doaj.org/article/002ad306ab4241e18b1f04d4f7cc328f
Autor:
A. V. Tereshchenko, N. M. Shilov, N. N. Yudina, Yu. A. Sidorova, E. V. Erokhina, S. V. Novikov, A. N. Mits
Publikováno v:
Oftalʹmologiâ, Vol 20, Iss 2, Pp 245-252 (2023)
The purpose: to develop a technology for the surgical treatment of macular retinal tears using an “effective” fragment of the ILM with an optimal shape, size, and localization, and evaluate its anatomical and functional efficiency.Methods. There
Externí odkaz:
https://doaj.org/article/be6b17eeefed4842b730aa2da6ab2de7
Publikováno v:
Русский журнал детской неврологии, Vol 18, Iss 1, Pp 22-37 (2023)
Myotonic dystrophy type 1 (DM1) is one of the most common neuromuscular diseases with an autosomal dominant type of inheritance associated with expansion in the DMPK gene. A distinctive feature of the disease is the presence of muscle symptoms and mu
Externí odkaz:
https://doaj.org/article/8aa1ab119b1e4691bb8191b124dcd5ae
Publikováno v:
Oftalʹmologiâ, Vol 20, Iss 1, Pp 112-119 (2023)
The purpose — to study the features of the foveal avascular zone (FAZ) in children with active retinopathy of prematurity according to the data of optical coherence tomography in angio-mode.Patients and methods. OCT-A was performed on 37 premature
Externí odkaz:
https://doaj.org/article/53f14299a6fe4a8daf5537e36568b4c3
Publikováno v:
Российский офтальмологический журнал, Vol 16, Iss 1, Pp 82-89 (2023)
Purpose: to evaluate the effectiveness of combined treatment of chronic central serous chorioretinopathy (CSCRP) complicated by type 1 choroidal neovascularization (CNV) by subthreshold micropulse laser exposure (SMILE) and intravitreal injection of
Externí odkaz:
https://doaj.org/article/607ecf50b207425fa6faec34bb468ec1
Publikováno v:
Российский офтальмологический журнал, Vol 15, Iss 4, Pp 95-101 (2022)
Purpose: to study the state of blood flow in the ocular arteries of patients with various forms, stages and course types of active retinopathy of prematurity (ROP). Material and methods. Colour duplex scanning was performed by colour Doppler mapping
Externí odkaz:
https://doaj.org/article/161dd3c34d7242c08d36c15028375cb3
Publikováno v:
Российский офтальмологический журнал, Vol 15, Iss 2, Pp 120-129 (2022)
Purpose: to evaluate the degree of structural lesions of the microvasculature, depending on the stage and type of active ROP with optical coherence tomography (OCT) in angio-mode (OCTA). Material and methods. 63 premature infants (63 eyes) with activ
Externí odkaz:
https://doaj.org/article/fa9b5233fe2c42029c10c32505bb11ec
Autor:
A. V. Tereshchenko, I. G. Trifanenkova, N. N. Yudina, M. S. Tereshchenkova, E. V. Erokhina, Yu. A. Sidorova
Publikováno v:
Acta Biomedica Scientifica, Vol 6, Iss 6-1, Pp 96-104 (2021)
Background. The anatomical and functional results of surgery for retinopathy of prematurity (ROP) are determined not only by the stage of the pathological process, but also depend on the timing of its implementation.The aim: to estimate the effective
Externí odkaz:
https://doaj.org/article/baafc98aed9b4426bfed63f466db912e