Vitaliy A. Kadyshev

1 Moskvorech'e St, 115522
Moscow, MOW, Russian Federation

Last Updated: 09/26/2026

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Found 15 publications

Results of the multicenter study "Registry of patients with inherited retinal dystrophies caused by confirmed biallelic mutations in the RPE65 and RLBP1 genes in Russia (REGINA)". Report 1. Molecular genetic characteristics of inherited retinal pathologies

Results of the multicenter study "Registry of patients with inherited retinal dystrophies caused by confirmed biallelic mutations in the RPE65 and RLBP1 genes in Russia (REGINA)". Report 1. Molecular genetic characteristics of inherited retinal pathologies

Journal: Vestnik oftalmologii

Published: March 18, 2026

Results of the multicenter study "Registry of patients with inherited retinal dystrophies caused by confirmed biallelic mutations in the RPE65 and RLBP1 genes in Russia (REGINA)". Report 2. Clinical, social and demographic characteristics of inherited retinal pathologies

Results of the multicenter study "Registry of patients with inherited retinal dystrophies caused by confirmed biallelic mutations in the RPE65 and RLBP1 genes in Russia (REGINA)". Report 2. Clinical, social and demographic characteristics of inherited retinal pathologies

Journal: Vestnik oftalmologii

Published: March 18, 2026

Genetic Features of Albinism: A Comprehensive Analysis in the Russian Population.

Genetic Features of Albinism: A Comprehensive Analysis in the Russian Population.

Journal: Pigment cell & melanoma research

Published: June 19, 2025

Common Variants in the TYR Gene with Unclear Pathogenicity as the Cause of Oculocutaneous Albinism in a Cohort of Russian Patients.

Common Variants in the TYR Gene with Unclear Pathogenicity as the Cause of Oculocutaneous Albinism in a Cohort of Russian Patients.

Journal: Biomedicines

Published: July 28, 2024

Molecular genetics in diagnosis of Coats disease: combination of oligogenic variants associated with different forms of hereditary retinal dystrophy

Molecular genetics in diagnosis of Coats disease: combination of oligogenic variants associated with different forms of hereditary retinal dystrophy

Journal: Vestnik oftalmologii

Published: March 16, 2023

Stroke in children and adolescents

Stroke in children and adolescents

Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova

Published: December 30, 2022

Gyrate atrophy of the choroid and retina with ornithinemia and foveoschisis (clinical observation)

Gyrate atrophy of the choroid and retina with ornithinemia and foveoschisis (clinical observation)

Journal: Vestnik oftalmologii

Published: October 26, 2022

Inherited retinal dystrophy: first results of RPE65 gene replacement therapy in Russia

Inherited retinal dystrophy: first results of RPE65 gene replacement therapy in Russia

Journal: Vestnik oftalmologii

Published: August 25, 2022

Analysis of associations of undifferentiated connective tissue dysplasia with the development of primary open-angle glaucoma. Clinical and genetic aspects

Analysis of associations of undifferentiated connective tissue dysplasia with the development of primary open-angle glaucoma. Clinical and genetic aspects

Journal: Vestnik oftalmologii

Published: December 29, 2021

Epidemiology of spontaneous nasal, ear and throat bleedings

Epidemiology of spontaneous nasal, ear and throat bleedings

Journal: Vestnik otorinolaringologii

Published: September 09, 2021

Fundus albipunctatus with mutations in the RDH5 gene (clinical case)

Fundus albipunctatus with mutations in the RDH5 gene (clinical case)

Journal: Vestnik oftalmologii

Published: February 21, 2021

Quincke's edema or angioedema. A contemporary view of the problem

Quincke's edema or angioedema. A contemporary view of the problem

Journal: Vestnik otorinolaringologii

Published: November 03, 2020

Showing 1-12 of 15

Last Updated: 09/26/2026