Leber’s Congenital Amaurosis and its Complications – A Very Rare Presentation by Sujit Das, Sakshi Singh, Aastha Agarwal, Ram Monohar Misra

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Retinal dysfunction finding after uneventful cataract surgery with extended depth-of-focus intraocular lens by Frederico França Marques, Guilherme Bufarah, Daniela Meira Villano Marques, Bernardo Kaplan Moscovici, Daniel Diniz Da Gama, Sung Eun Song Watanabe, Octaviano Magalhaes Junior

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Endoplasmic reticulum stress and rhodopsin accumulation in an organoid model of Retinitis Pigmentosa carrying a RHO pathogenic variant by Arnau Navinés-Ferrer, Esther Pomares

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Small molecule treatment alleviates photoreceptor cilia defects in LCA5-deficient human retinal organoids by Dimitra Athanasiou, Tess A. V. Afanasyeva, Niuzheng Chai, Kalliopi Ziaka, Katarina Jovanovic, Rosellina Guarascio, Karsten Boldt, Julio C. Corral-Serrano, Naheed Kanuga, Ronald Roepman, Rob W. J. Collin, Michael E. Cheetham

Subjects: “…Retinal dystrophy…”
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Classifications of peripheral retinal dystrophies by O.M. Stanishevskaya, M.A. Glock, M.A. Safronova, A.I. Belyaeva, D.V. Chernykh

Subjects: “…peripheral retinal dystrophy…”
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Current understanding on Retinitis Pigmentosa: a literature review by Naning Suleman

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Early-Onset Retinal Dysfunction Associated with Novel WDR19 Variants in Sensenbrenner Syndrome by Bogumiła Wójcik-Niklewska, Zofia Oliwa, Zofia Zdort, Adrian Smędowski

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C21orf2 variants causing inherited retinal disease: A review of what we know and a report of two new suspected cases by Meagan Shinbashi, Ann Jewell, Jessica Randolph, Natario Couser

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A Review of the Ocular Phenotype and Correlation with Genotype in Poretti–Boltshauser Syndrome by Won Young Moon, Sanil Shah, Nervine ElMeshad, Samantha R. De Silva

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Study of Frequency and Nosology of Clinical Varieties of Retinal Dystrophies in Children and Adolescents by O. V. Kolenko, E. L. Sorokin, A. V. Sergeeva

Subjects: “…retinal dystrophies…”
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The Role of Electrical Stimulation in Management of Retinal and Optic Nerve Degenerative and Dystrophic Disorders. Literature Review by L. S. Pateyuk, A. K. Drakon, V. M. Sheludchenko, N. B. Korchazhkina

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Enhanced genotype-phenotype analysis using multimodal adaptive optics and 3D protein structure in Bietti Crystalline Dystrophy by Aarushi Kumar, Young Joo Sun, Ditte K. Rasmussen, Aubrey Hargrave, Claudia Phillips, Jennifer T. Vu, Mauricio G.S. Costa, Loh-Shan B. Leung, Charles Yu, Alfredo Dubra, Vinit B. Mahajan

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Idiopathic Infantile Nystagmus; Genetics foundation and Clinical association by Basamat AlMoallem

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Expansion of genotypic and phenotypic findings in ADAMTS18-related ocular pathology by Ari H. August, Rebecca A. Procopio, Christopher J. Rapuano, José S. Pulido

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Gene therapy in hereditary retinal dystrophy by Jia-Ying Chien, Shun-Ping Huang

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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

Subjects: “…inherited retinal dystrophy…”
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Identification and functional characterization of ABCA4 gene variants in three patients with Stargardt disease or retinitis pigmentosa by Qi Luo, Juan Huang, Lu Shi, Lu Shi, Guanghong Zhang, Linping Xue, Kehu Wu, Xiaoyu Li, Lei Yang, Dujun Li, Liangwei Mao, Jihong Luo

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Ocular hemodynamics in patients with rhegmatogenous retinal detachment by N. H. Zavgorodnya, A. V. Dedov, Ye. M. Ivakhnenko

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Expanding Genetic and Clinical Spectra of Inherited Retinal Dystrophies: Identification of Three Novel <i>PRPH2</i> Variants by Raffaella Cascella, Jacopo Sebastiani, Claudia Strafella, Giulia Calvino, Sarah Andreucci, Michele D’ambrosio, Stefania Zampatti, Jung Hee Levialdi Ghiron, Benedetto Falsini, Andrea Cusumano, Emiliano Giardina

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Rescue of the disease-associated phenotype in CRISPR-corrected hiPSCs as a therapeutic approach for inherited retinal dystrophies by Laura Siles, Esther Pomares

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