I. V. Zolnikova

发表

[Thickness of the retinal photoreceptor layers and the choroid, and bioelectrical activity of the macula in retinitis pigmentosa].

I. V. Egorova, E. V. Rogatina, S. Y. Rogova, 2019, Vestnik oftalmologii.

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

D. Barh, I. V. Zolnikova, A. Demchinsky, 2021 .

The spectrum of mutations in the patients presenting with ABCA4-associated Stargardt's disease in a Russian population

M. E. Ivanova, V. Strelnikov, O. Demenkova, 2016 .

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

A. Marakhonov, S. Kutsev, N. Urakova, 2021, Ophthalmology in Russia.

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

I. V. Zolnikova, S. Milash, V. Kadyshev, 2020, Russian Ophthalmological Journal.

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

S. Kutsev, V. Neroev, I. V. Zolnikova, 2021, Russian Ophthalmological Journal.

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

R. Zinchenko, I. V. Egorova, S. Y. Rogova, 2019, Ophthalmology in Russia.

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

M. E. Ivanova, I. Kanivets, A. Antonets, 2020 .

Macular Electroretinography and Methods of Retina Visualization in Diagnostics of Standard Stargardt Disease, Verified by Molecular Genetic Methods

M. E. Ivanova, V. Izhevskaya, V. Strelnikov, 2014 .

Stargardt disease-associated mutation spectrum of a Russian Federation cohort.

M. E. Ivanova, D. Barh, V. Strelnikov, 2017, European journal of medical genetics.

Novel frameshift mutation in NYX gene in a Russian family with complete congenital stationary night blindness

M. E. Ivanova, D. Barh, P. Ghosh, 2019, Ophthalmic genetics.

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

R. Zinchenko, A. Stepanova, I. V. Egorova, 2022, Vestnik oftalmologii.

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

A. Marakhonov, E. Denisova, R. Zinchenko, 2021, Russian Ophthalmological Journal.

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

A. Marakhonov, S. Kutsev, R. Zinchenko, 2021, Ophthalmology in Russia.

A new method of amblyopia treatment in children with unstable central and eccentric fixation using biofeedback

E. Tarutta, I. V. Zolnikova, S. Milash, 2022, Russian Ophthalmological Journal.

A comparative study of structural, functional and circulatory parameters in glaucoma diagnostics

A. V. Fomin, N. Kurysheva, E. V. Maslova, 2018, PloS one.

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

E. Denisova, V. Neroev, I. V. Zolnikova, 2023, Russian Ophthalmological Journal.

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

A. Stepanova, I. V. Zolnikova, V. Kadyshev, 2022, Vestnik oftalmologii.