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

por S. V. Milash, I. V. Zolnikova, V. V. Kadyshev
Publicado em 2020-12-01

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

por I. V. Zolnikova, V. V. Kadyshev, A. V. Marakhonov, S. I. Kutsev, R. A. Zinchenko
Publicado em 2021-04-01

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

por V. V. Neroev, L. A. Katargina, V. V. Kadyshev, I. V. Zolnikova, S. I. Kutsev
Publicado em 2021-09-01

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

por I. V. Zolnikova, O. N. Demenkova, E. V. Rogatina, D. V. Levina, I. V. Egorova, S. Yu. Rogova
Publicado em 2018-10-01

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

por M. E. Ivanova, K. V. Gorgisheli, I. V. Zolnikova, D. S. Atarshchikov, D. Barh, Zh. M. Salmasi, L. M. Balashova
Publicado em 2019-08-01

Retinal Postphotoreceptor Layers and Macular Electroretinogram in Retinitis Pigmentosa

por I. V. Zolnikova, S. V. Milash, A. B. Chernyak, D. V. Levina, I. V. Egorova, E. V. Rogatina, E. A. Eremeeva, S. Y. Rogova
Publicado em 2020-04-01

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

por M. E. Weener, D. S. Atarshchikov, V. V. Kadyshev, I. V. Zolnikova, A. M. Demchinsky, D. Barh, L. M. Balashova, J. M. Salmasi
Publicado em 2021-03-01

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

por L. A. Katargina, V. V. Kadyshev, E. V. Denisova, E. A. Geraskina, A. V. Marakhonov, S. A. Garifullina, I. V. Zolnikova, R. A. Zinchenko
Publicado em 2022-01-01

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

por 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
Publicado em 2018-10-01

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

por 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
Publicado em 2019-03-01

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

por 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
Publicado em 2021-12-01

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

por 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
Publicado em 2020-03-01