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Inhibiting autophagy reduces retinal degeneration caused by protein misfolding

Autophagy, 2018-07, Vol.14 (7), p.1226-1238

2018

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Prolonged Inner Retinal Photoreception Depends on the Visual Retinoid Cycle

The Journal of neuroscience, 2016-04, Vol.36 (15), p.4209-4217

2016

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Autophagy-mediated catabolism of visual transduction proteins prevents retinal degeneration

Autophagy, 2016-12, Vol.12 (12), p.2439-2450

2016

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Rd9 is a naturally occurring mouse model of a common form of retinitis pigmentosa caused by mutations in RPGR-ORF15

PloS one, 2012-05, Vol.7 (5), p.e35865-e35865

2012

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Autoimmune retinopathy associated with monoclonal gammopathy of undetermined significance: a case report

BMC ophthalmology, 2020-04, Vol.20 (1), p.153-153, Article 153

2020

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Contrast sensitivity deficits in patients with mutation-proven inherited retinal degenerations

BMC ophthalmology, 2018-12, Vol.18 (1), p.313-313, Article 313

2018

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A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degeneration

Human molecular genetics, 2011-05, Vol.20 (10), p.2000-2014

2011

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Distinct signature of altered homeostasis in aging rod photoreceptors: implications for retinal diseases

PloS one, 2010-11, Vol.5 (11), p.e13885-e13885

2010

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Acute panretinal structural and functional abnormalities after intravitreous ocriplasmin injection

JAMA ophthalmology, 2014-04, Vol.132 (4), p.484

2014

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Inherited Retinal Degeneration: Genetics, Disease Characterization, and Outcome Measures

Journal of ophthalmology, 2017-01, Vol.2017, p.2109014-2

2017

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Macular hyperpigmentary changes in ABCA4 -Stargardt disease

International journal of retina and vitreous, 2019-04, Vol.5 (1), p.9-9, Article 9

2019

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Rapid visual field constriction in a patient with retinitis pigmentosa and pituitary adenoma

American journal of ophthalmology case reports, 2020-09, Vol.19, p.100762, Article 100762

2020

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Adherence and satisfaction in Argus II prosthesis users: a self determination theory model

Ophthalmic genetics, 2022-08, Vol.43 (4), p.1-469

2022

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Gene Supplementation in Mice Heterozygous for the D477G RPE65 Variant Implicated in Autosomal Dominant Retinitis Pigmentosa

Human gene therapy, 2023-07, Vol.34 (13-14), p.639-648

2023

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Detailed clinical characterisation, unique features and natural history of autosomal recessive RDH12-associated retinal degeneration

British journal of ophthalmology, 2019-12, Vol.103 (12), p.1789-1796

2019

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ISCEV extended protocol for the photopic On–Off ERG

Documenta ophthalmologica, 2018-06, Vol.136 (3), p.199-206

2018

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Establishing baseline rod electroretinogram values in achromatopsia and cone dystrophy

Documenta ophthalmologica, 2012-12, Vol.125 (3), p.229-233

2012

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Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium

Investigative ophthalmology & visual science, 2015-02, Vol.56 (2), p.918-931

2015

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Development of a Gene Therapy Vector for RDH12 -Associated Retinal Dystrophy

Human gene therapy, 2019-11, Vol.30 (11), p.1325-1335

2019

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Excess cones in the retinal degeneration rd7 mouse, caused by the loss of function of orphan nuclear receptor Nr2e3, originate from early-born photoreceptor precursors

Human molecular genetics, 2011-11, Vol.20 (21), p.4102-4115

2011

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Calculation of test-retest variability in phase I/IIa clinical trials for Inherited Retinal Degenerations

Ophthalmic genetics, 2021-06, Vol.42 (3), p.283-290

2021

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Multifocal visual evoked potentials for early glaucoma detection

Ophthalmic surgery, lasers & imaging, 2012-07, Vol.43 (4), p.335-340

2012

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Diagnostic Fundus Autofluorescence Patterns in Achromatopsia

American journal of ophthalmology, 2013-12, Vol.156 (6), p.1211-1219.e2

2013

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Inhibiting autophagy reduces retinal degeneration caused by protein misfolding

Prolonged Inner Retinal Photoreception Depends on the Visual Retinoid Cycle

Autophagy-mediated catabolism of visual transduction proteins prevents retinal degeneration

Rd9 is a naturally occurring mouse model of a common form of retinitis pigmentosa caused by mutations in RPGR-ORF15

Autoimmune retinopathy associated with monoclonal gammopathy of undetermined significance: a case report

Contrast sensitivity deficits in patients with mutation-proven inherited retinal degenerations

A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degeneration

Distinct signature of altered homeostasis in aging rod photoreceptors: implications for retinal diseases

Acute panretinal structural and functional abnormalities after intravitreous ocriplasmin injection

Inherited Retinal Degeneration: Genetics, Disease Characterization, and Outcome Measures

Macular hyperpigmentary changes in ABCA4 -Stargardt disease

Rapid visual field constriction in a patient with retinitis pigmentosa and pituitary adenoma

Adherence and satisfaction in Argus II prosthesis users: a self determination theory model

Gene Supplementation in Mice Heterozygous for the D477G RPE65 Variant Implicated in Autosomal Dominant Retinitis Pigmentosa

Detailed clinical characterisation, unique features and natural history of autosomal recessive RDH12-associated retinal degeneration

ISCEV extended protocol for the photopic On–Off ERG

Establishing baseline rod electroretinogram values in achromatopsia and cone dystrophy

Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis

Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium

Development of a Gene Therapy Vector for RDH12 -Associated Retinal Dystrophy

Excess cones in the retinal degeneration rd7 mouse, caused by the loss of function of orphan nuclear receptor Nr2e3, originate from early-born photoreceptor precursors

Calculation of test-retest variability in phase I/IIa clinical trials for Inherited Retinal Degenerations

Multifocal visual evoked potentials for early glaucoma detection

Diagnostic Fundus Autofluorescence Patterns in Achromatopsia

Advancing Clinical Trials for Inherited Retinal Diseases: Recommendations from the Second Monaciano Symposium

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