Multimodal imaging of hereditary retinal dystrophies (a series of clinical cases) by S. V. Milash, I. V. Zolnikova, V. V. Kadyshev

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Аutosomal Dominant Oculodental-Digital Dysplasia with Mutation in Gene GJA1 (Clinical Case) by I. V. Zolnikova, V. V. Kadyshev, A. V. Marakhonov, S. I. Kutsev, R. A. Zinchenko

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Prospects for the diagnosis and gene therapy of inherited retinal dystrophies caused by biallelic mutations in the RPE65 gene by V. V. Neroev, L. A. Katargina, V. V. Kadyshev, I. V. Zolnikova, S. I. Kutsev

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Bioelectric Activity of the Macula and Light Sensitivity in Retinitis Pigmentosa with Foveal Atrophy and Cystoid Macular Oedema by I. V. Zolnikova, O. N. Demenkova, E. V. Rogatina, D. V. Levina, I. V. Egorova, S. Yu. Rogova

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A new method of amblyopia treatment in children with unstable central and eccentric fixation using biofeedback by E. P. Tarutta, R. R. Khubieva, S. V. Milash, A. V. Apaev, N. A. Aklaeva, I. V. Zolnikova

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Pathogenesis and clinical features of congenital stationary night blindness in case of c.283delC NYX gene mutation by M. E. Ivanova, K. V. Gorgisheli, I. V. Zolnikova, D. S. Atarshchikov, D. Barh, Zh. M. Salmasi, L. M. Balashova

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Retinal Postphotoreceptor Layers and Macular Electroretinogram in Retinitis Pigmentosa by I. V. Zolnikova, S. V. Milash, A. B. Chernyak, D. V. Levina, I. V. Egorova, E. V. Rogatina, E. A. Eremeeva, S. Y. Rogova

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Pathophysiological features of the visual cycle, cascade and metabolic pathways in retinitis pigmentosa by M. E. Weener, D. S. Atarshchikov, V. V. Kadyshev, I. V. Zolnikova, A. M. Demchinsky, D. Barh, L. M. Balashova, J. M. Salmasi

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Clinical manifestations of familial exudative vitreoretinopathy in children with nucleotide sequence alterations in the FZD4 gene by L. A. Katargina, V. V. Kadyshev, E. V. Denisova, E. A. Geraskina, A. V. Marakhonov, S. A. Garifullina, I. V. Zolnikova, R. A. Zinchenko

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

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

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

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Case of phenotype of optic nerve atrophy due to mutation in С19orf12 gene (neurodegeneration with the brain iron accumulation (nbia)) by M.E. Ivanova, V.V. Kadyshev, D.S. Atarshchikov, I.V. Zolnikova, N.P. Akchurina, N.K. Serova, F.A. Konovalov, E.R. Lozier, E.A. Pomerantseva, N.V. Vetrova, D. Barh, L.M. Balashova, J.M. Salmasi

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

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