Search Results - V. V. Kadyshev

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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Genetic Epidemiology of Primary Congenital Glaucoma in the World. Part I by Zh. G. Oganezova, V. V. Kadyshev, E. A. Egorov

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Genetic Epidemiology of Primary Congenital Glaucoma in the World. Part II by Zh. G. Oganezova, V. V. Kadyshev, E. A. Egorov

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Economic outcomes of centralized procurements of gene therapy for patients with orphan diseases: inherited retinal dystrophy by N. А. Avxentyev, Yu. V. Makarova, 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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A decision making algorithm for inherited retinal dystrophies, caused by biallelic mutations in the RPE65 gene, in the clinical practice of an ophthalmologist by E. I. Saidasheva, V. V. Kadyshev, V. V. Brzheskiy, N. A. Malinovskaya, K. K. Shefer

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Genetic variants of congenital glaucoma. Analysis of the literature and description of the clinical case by L. A. Katargina, V. V. Kadyshev, A. A. Sorokin, A. V. Pleskova, R. A. Zinchenko

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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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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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SPECTRUM OF MOLECULAR GENETIC ALTERATIONS AND DIVERSITY OF CLINICAL FORMS OF STARGARDT DISEASE by N. L. Sheremet, I. G. Grushke, N. V. Zhorzholadze, I. A. Ronzina, A. A. Mikaelyan, S. A. Kurbatov, V. V. Kadyshev, K. I. Anoshkin, V. V. Strelnikov

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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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First results of long-term follow-up of children in Russia after gene therapy for hereditary retinal dystrophies associated with biallelic mutations in the RPE65 gene by V. V. Neroev, L. A. Katargina, M. P. Kharlampidi, L. V. Kogoleva, I. V. Zolnikova, P. A. Ilyukhin, E. V. Denisova, S. V. Milash, N. A. Osipova, S. I. Kutsev, A. V. Polyakov, R. A. Zinchenko, V. V. Kadyshev, Yu. A. Bobrovskaya

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