Multimodal imaging of hereditary retinal dystrophies (a series of clinical cases)

بواسطة S. V. Milash, I. V. Zolnikova, V. V. Kadyshev
منشور في 2020-12-01

Аutosomal Dominant Oculodental-Digital Dysplasia with Mutation in Gene GJA1 (Clinical Case)

بواسطة I. V. Zolnikova, V. V. Kadyshev, A. V. Marakhonov, S. I. Kutsev, R. A. Zinchenko
منشور في 2021-04-01

Prospects for the diagnosis and gene therapy of inherited retinal dystrophies caused by biallelic mutations in the RPE65 gene

بواسطة V. V. Neroev, L. A. Katargina, V. V. Kadyshev, I. V. Zolnikova, S. I. Kutsev
منشور في 2021-09-01

Bioelectric Activity of the Macula and Light Sensitivity in Retinitis Pigmentosa with Foveal Atrophy and Cystoid Macular Oedema

بواسطة I. V. Zolnikova, O. N. Demenkova, E. V. Rogatina, D. V. Levina, I. V. Egorova, S. Yu. Rogova
منشور في 2018-10-01

Pathogenesis and clinical features of congenital stationary night blindness in case of c.283delC NYX gene mutation

بواسطة M. E. Ivanova, K. V. Gorgisheli, I. V. Zolnikova, D. S. Atarshchikov, D. Barh, Zh. M. Salmasi, L. M. Balashova
منشور في 2019-08-01

Retinal Postphotoreceptor Layers and Macular Electroretinogram in Retinitis Pigmentosa

بواسطة I. V. Zolnikova, S. V. Milash, A. B. Chernyak, D. V. Levina, I. V. Egorova, E. V. Rogatina, E. A. Eremeeva, S. Y. Rogova
منشور في 2020-04-01

Pathophysiological features of the visual cycle, cascade and metabolic pathways in retinitis pigmentosa

بواسطة M. E. Weener, D. S. Atarshchikov, V. V. Kadyshev, I. V. Zolnikova, A. M. Demchinsky, D. Barh, L. M. Balashova, J. M. Salmasi
منشور في 2021-03-01

Clinical manifestations of familial exudative vitreoretinopathy in children with nucleotide sequence alterations in the FZD4 gene

بواسطة L. A. Katargina, V. V. Kadyshev, E. V. Denisova, E. A. Geraskina, A. V. Marakhonov, S. A. Garifullina, I. V. Zolnikova, R. A. Zinchenko
منشور في 2022-01-01

Electroretinography and OCT angiography of the retina and optic nerve in retinitis pigmentosa

بواسطة V. . Zolnikova, D. V. Levina, T. D. Okhotsimskaya, V. A. Fadeeva, I. V. Egorova, E. V. Rogatina, E. A. Eremeeva, O. N. Demenkova, S. Yu. Rogova
منشور في 2018-10-01

Choroideremia with Mutation in CHM Gene. Clinical Cases with Literature Review

بواسطة I. V. Zolnikova, S. V. Milash, V. V. Kadyshev, A. B. Chernyak, D. V. Levina, R. A. Zinchenko, I. V. Egorova, E. A. Eremeeva, S. Y. Rogova
منشور في 2019-03-01

Clinical and Genetic Correlations of Inherital Retinal Disease with Mutations in the ABCA4 Gene by Patients of the Russian Population

بواسطة I. V. Zolnikova, V. V. Kadyshev, A. V. Marakhonov, A. B. Chernyak, S. V. Milash, Yu. A. Bobrovskaya, N. A. Urakova, N. Sh. Kokoeva, S. I. Kutsev, R. A. Zinchenko
منشور في 2021-12-01

Epidemiologic, clinical and pathogenesis features of achromatopsia in the Russian population

بواسطة M. E. Ivanova, I. V. Zolnikova, I. E. Khatsenko, V. V. Strelnikov, F. A. Konovalov, E. R. Lozier, M. A. Ampleeva, A. V. Antonets, I. V. Kanivets, K. V. Gorgisheli, D. S. Atarshchikov, D. V. Pyankov, S. A. Korostelev, E. B. Kuznetsova, D. Bar, L. M. Balashova, Zh. M. Salmasi
منشور في 2020-03-01