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Page 1
Previously Unclassified Mutation of mtDNA m.3472T>C: Evidence of Pathogenicity in Leber's Hereditary Optic Neuropathy.
Sheremet NL, Nevinitsyna TA, Zhorzholadze NV, Ronzina IA, Itkis YS, Krylova TD, Tsygankova PG, Malakhova VA, Zakharova EY, Tokarchuk AV, Panteleeva AA, Karger EM, Lyamzaev KG, Avetisov SE. Sheremet NL, et al. Among authors: zhorzholadze nv. Biochemistry (Mosc). 2016 Jul;81(7):748-54. doi: 10.1134/S0006297916070117. Biochemistry (Mosc). 2016. PMID: 27449621 Free article.
[Molecular genetic diagnosis of Stargardt disease].
Sheremet NL, Zhorzholadze NV, Ronzina IA, Grushke IG, Kurbatov SA, Chukhrova AL, Loginova AN, Shcherbakova PO, Tanas AS, Polyakov AV, Strel'nikov VV. Sheremet NL, et al. Among authors: zhorzholadze nv. Vestn Oftalmol. 2017;133(4):4-11. doi: 10.17116/oftalma201713344-11. Vestn Oftalmol. 2017. PMID: 28980559 Free article. Russian.
[Torpedo macu-lopathy (clinical case)].
Stoyukhina AS, Zhorzholadze NV, Danilov SS. Stoyukhina AS, et al. Among authors: zhorzholadze nv. Vestn Oftalmol. 2017;133(5):56-63. doi: 10.17116/oftalma2017133556-62. Vestn Oftalmol. 2017. PMID: 29165414 Russian.
[Inherited retinal diseases in patients with ABCA4 gene mutations].
Sheremet NL, Grushke IG, Zhorzholadze NV, Tanas AS, Strelnikov VV. Sheremet NL, et al. Among authors: zhorzholadze nv. Vestn Oftalmol. 2018;134(4):68-73. doi: 10.17116/oftalma201813404168. Vestn Oftalmol. 2018. PMID: 30166513 Review. Russian.
[Clinical polymorphism of splice site mutations in the ABCA4 gene].
Sheremet NL, Grushke IG, Zhorzholadze NV, Ronzina IA, Mikaelyan AA, Tanas AS, Strelnikov VV. Sheremet NL, et al. Among authors: zhorzholadze nv. Vestn Oftalmol. 2018;134(6):83-93. doi: 10.17116/oftalma201813406183. Vestn Oftalmol. 2018. PMID: 30721205 Russian.
22 results