Search Results - "Nevinitsyna, T. A."

Previously unclassified mutation of mtDNA m.3472T>C: Evidence of pathogenicity in Leber’s hereditary optic neuropathy by Sheremet, N. L., Nevinitsyna, T. A., Zhorzholadze, N. V., Ronzina, I. A., Itkis, Y. S., Krylova, T. D., Tsygankova, P. G., Malakhova, V. A., Zakharova, E. Y., Tokarchuk, A. V., Panteleeva, A. A., Karger, E. M., Lyamzaev, K. G., Avetisov, S. E.

“…Leber’s hereditary optic neuropathy (LHON) refers to a group of mitochondrial diseases and is characterized by defects of the mitochondrial electron transport…”
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High-Resolution Respirometry in Diagnostics of Mitochondrial Diseases Caused by Mitochondrial Complex I Deficiency by Krylova, T. D., Tsygankova, P. G., Itkis, Y. S., Sheremet, N. L., Nevinitsyna, T. A., Mikhaylova, S. V., Zakharova, E. Y.

“…Mitochondrial complex I deficiency (CID) is one of the most common defects in the OXPHOS system; it represents more than 30% cases of mitochondrial diseases…”
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Modern opportunities and prospects for studying pathogenesis, diagnosing and treating hereditary optic neuropathies by Sheremet, N L, Khanakova, N A, Nevinitsyna, T A, Tsygankova, P G, Itkis, Iu S, Krylova, T D, Loginova, A N, Chukhrova, A L, Venkova, L S, Svistunova, D M, Chernoivanenko, I S, Zakharova, E Iu, Poliakov, A V, Minin, A A

“…To evaluate modern opportunities and prospects for studying pathogenesis and improving diagnostics and treatment of hereditary optic neuropathies (HON). The…”
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Electrophysiological and psychophysical studies in assessment of visual functions in patients with hereditary optic neuropathy by Sheremet, N L, Ronzina, I A, Andreeva, N A, Zhorzholadze, N V, Murakhovskaya, Yu K, Nevinitsyna, T A, Shmelkova, M S, Krylova, T D, Tsygankova, P G, Gerasimidi, E S, Lyamzaev, K G, Skulachev, M V, Karger, E M

“…To study the capabilities of electrophysiological and psychophysical examination methods for assessment of the functional state of ganglion cells, retina and…”
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