Zobrazeno 1 - 10
of 24
pro vyhledávání: '"N V Zhorzholadze"'
Autor:
A. K. Kalashnikova, D. D. Eliseeva, N. A. Andreeva, N. V. Zhorzholadze, I. A. Ronzina, R. Ts. Bembeeva, N. N. Venediktova, M. R. Kalganova, N. L. Sheremet
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 16, Iss 3, Pp 52-57 (2024)
The discovery of antibodies against aquaporin-4 (AQP4) and against myelinoligodendrocyte glycoprotein (MOG) confirmed the existence of two disease entities distinct from multiple sclerosis (MS) — neuromyelitis optica spectrum disorders (NMOSD) and
Externí odkaz:
https://doaj.org/article/fd515cc5e10f4901936cdc4c615f82f4
Autor:
N. L. Sheremet, D. D. Eliseeva, V. V. Bryukhov, N. A. Andreeva, N. V. Zhorzholadze, Yu. K. Murakhovskaya, A. K. Kalashnikova, M. N. Zakharova
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 15, Iss 0, Pp 35-42 (2023)
Optic neuritis (ON) can often occur at the onset of a demyelinating autoimmune CNS disease or as one of its clinical manifestations. The introduction of novel laboratory techniques, technical advances in magnetic resonance imaging (MRI), electrophysi
Externí odkaz:
https://doaj.org/article/d61eef3ed1224fd9b78789cd5dc80416
Autor:
N. L. Sheremet, I. G. Grushke, N. V. Zhorzholadze, I. A. Ronzina, A. A. Mikaelyan, S. A. Kurbatov, V. V. Kadyshev, K. I. Anoshkin, V. V. Strelnikov
Publikováno v:
Сибирский научный медицинский журнал, Vol 38, Iss 5, Pp 65-71 (2019)
Purpose of the study was to assess the spectrum of molecular genetic disorders and the variety of clinical forms in patients with Stargardt disease. Material and methods. 56 patients aged 15-44 years who had been diagnosed with Stargardt disease in a
Externí odkaz:
https://doaj.org/article/dd9051f9de144ecca4e63b03284bd4cb
Autor:
N L, Sheremet, N A, Andreeva, N V, Zhorzholadze, Yu K, Murakhovskaya, M S, Shmelkova, T D, Krylova, P G, Tsygankova
Publikováno v:
Vestnik oftalmologii. 138(4)
Folate metabolism disorders are known to have a potential involvement in the pathophysiology of mitochondrial diseases. Many researchers suggest that profound systemic folate deficiency may contribute to mitochondrial folate deficiency. Folic acid me
Autor:
I.A. Ronzina, А.А. Mikaelyan, K.I. Anoshkin, V.V. Strelnikov, A.S. Tanas, N.L. Sheremet, N V Zhorzholadze, I.G. Grushke
Publikováno v:
POINT OF VIEW. EAST – WEST. :54-57
Publikováno v:
Vestnik oftalmologii. 137(5)
Unilateral pigmentary retinopathy (PR) is a rare, atypical form of hereditary retinal pathology. Different types of secondary retinopathy associated with various non-hereditary diseases, trauma or intoxication can imitate unilateral PR. Therefore, it
Publikováno v:
Bulletin of Pirogov National Medical & Surgical Center. 16:145-147
Autor:
A.S. Tanas, А.А. Mikaelyan, N.L. Sheremet, K.I. Anoshkin, N V Zhorzholadze, I.G. Grushke, I.A. Ronzina, V.V. Strelnikov
Publikováno v:
Modern technologies in ophtalmology. :63-67
Autor:
S.L. Kiselev, A.A. Mikaelyan, I.G. Grushke, N.L. Sheremet, N V Zhorzholadze, I.A. Ronzina, Vladimir V Strelnikov
Publikováno v:
POINT OF VIEW. EAST – WEST. :71-75
Publikováno v:
Vestnik oftalmologii. 136(4. Vyp. 2)
To identify the specifics of structural and functional changes in patients with toxic optical neuropathy caused by acute methanol poisoning.One female patient with toxic optic neuropathy (TON), 2 male patients with partial optic atrophy caused by met