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Beneficial effects on vision in patients undergoing retinal gene therapy for choroideremia

Nature medicine, 2018-10, Vol.24 (10), p.1507

2018

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Gene therapy for visual loss: Opportunities and concerns

Progress in retinal and eye research, 2019-01, Vol.68, p.31-53

2019

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Visual Acuity after Retinal Gene Therapy for Choroideremia

The New England journal of medicine, 2016-05, Vol.374 (20), p.1996-1998

2016

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Interim Results of a Multicenter Trial with the New Electronic Subretinal Implant Alpha AMS in 15 Patients Blind from Inherited Retinal Degenerations

Frontiers in neuroscience, 2017-08, Vol.11, p.445-445

2017

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Correlation of Retinal Structure and Function in Choroideremia Carriers

Ophthalmology (Rochester, Minn.), 2015-06, Vol.122 (6), p.1274-1276

2015

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Genetic testing and gene therapy in retinal diseases: Knowledge and perceptions of optometrists in Australia and New Zealand

Clinical genetics, 2024-01, Vol.105 (1), p.34-43

2024

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Comparative analysis of loop-mediated isothermal amplification (LAMP)-based assays for rapid detection of SARS-CoV-2 genes

Scientific reports, 2021-11, Vol.11 (1), p.22493-22493, Article 22493

2021

Volltextzugriff (PDF)

Patient experiences and perceived value of genetic testing in inherited retinal diseases: a cross-sectional survey

Scientific reports, 2024-03, Vol.14 (1), p.5403-5403, Article 5403

2024

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Development of a CRISPRi Human Retinal Pigmented Epithelium Model for Functional Study of Age-Related Macular Degeneration Genes

International journal of molecular sciences, 2023-02, Vol.24 (4), p.3417

2023

Volltextzugriff (PDF)

Neuronal Reprogramming for Tissue Repair and Neuroregeneration

International journal of molecular sciences, 2020-06, Vol.21 (12), p.4273

2020

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Assessment of the Electronic Retinal Implant Alpha AMS in Restoring Vision to Blind Patients with End-Stage Retinitis Pigmentosa

Ophthalmology (Rochester, Minn.), 2018-03, Vol.125 (3), p.432-443

2018

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Endogenous spartin (SPG20) is recruited to endosomes and lipid droplets and interacts with the ubiquitin E3 ligases AIP4 and AIP5

Biochemical journal, 2009-09, Vol.423 (1), p.31-39

2009

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The Diagnostic Yield of Next Generation Sequencing in Inherited Retinal Diseases: A Systematic Review and Meta-analysis

American journal of ophthalmology, 2023-05, Vol.249, p.57-73

2023

Volltextzugriff (PDF)

Characterizing the Natural History of Visual Function in Choroideremia Using Microperimetry and Multimodal Retinal Imaging

Investigative ophthalmology & visual science, 2017-10, Vol.58 (12), p.5575-5583

2017

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Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners

Human molecular genetics, 2006-01, Vol.15 (2), p.307-318

2006

Volltextzugriff (PDF)

Assessing the carbon footprint of fluorinated gases in vitreoretinal surgery

Clinical & experimental ophthalmology, 2024-01, Vol.52 (1), p.113-115

2024

Volltextzugriff (PDF)

Female carriers of X-linked inherited retinal diseases – Genetics, diagnosis, and potential therapies

Progress in retinal and eye research, 2023-09, Vol.96, p.101190-101190, Article 101190

2023

Volltextzugriff (PDF)

Gene therapy for inherited retinal diseases: progress and possibilities

Clinical and experimental optometry, 2021-05, Vol.104 (4), p.444-454

2021

Volltextzugriff (PDF)

The Spectrum of CHM Gene Mutations in Choroideremia and Their Relationship to Clinical Phenotype

Investigative ophthalmology & visual science, 2016-11, Vol.57 (14), p.6033-6039

2016

Volltextzugriff (PDF)

The safety and efficacy of gene therapy treatment for monogenic retinal and optic nerve diseases: A systematic review

Genetics in medicine, 2022-03, Vol.24 (3), p.521-534

2022

Volltextzugriff (PDF)

First-in-Human Robot-Assisted Subretinal Drug Delivery Under Local Anesthesia

American journal of ophthalmology, 2022-05, Vol.237, p.104-113

2022

Volltextzugriff (PDF)

Discovery of Māori and Polynesian phototransduction pathway founder mutation: what is the gene and what does it mean?

Clinical & experimental ophthalmology, 2017-12, Vol.45 (9), p.854-856

Edwards, Thomas L

2017

Volltextzugriff (PDF)

Perspectives of carriers of X-linked retinal diseases on genetic testing and gene therapy: A global survey

Clinical genetics, 2024-02, Vol.105 (2), p.150-158

2024

Volltextzugriff (PDF)

Correlation of Optical Coherence Tomography and Autofluorescence in the Outer Retina and Choroid of Patients With Choroideremia

Investigative ophthalmology & visual science, 2016-07, Vol.57 (8), p.3674-3684

2016

Volltextzugriff (PDF)

Victorian evolution of inherited retinal diseases natural history registry (VENTURE study): Rationale, methodology and initial participant characteristics

Clinical & experimental ophthalmology, 2022-09, Vol.50 (7), p.768-780

2022

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Beneficial effects on vision in patients undergoing retinal gene therapy for choroideremia

Gene therapy for visual loss: Opportunities and concerns

Visual Acuity after Retinal Gene Therapy for Choroideremia

Interim Results of a Multicenter Trial with the New Electronic Subretinal Implant Alpha AMS in 15 Patients Blind from Inherited Retinal Degenerations

Correlation of Retinal Structure and Function in Choroideremia Carriers

Genetic testing and gene therapy in retinal diseases: Knowledge and perceptions of optometrists in Australia and New Zealand

Comparative analysis of loop-mediated isothermal amplification (LAMP)-based assays for rapid detection of SARS-CoV-2 genes

Patient experiences and perceived value of genetic testing in inherited retinal diseases: a cross-sectional survey

Development of a CRISPRi Human Retinal Pigmented Epithelium Model for Functional Study of Age-Related Macular Degeneration Genes

Neuronal Reprogramming for Tissue Repair and Neuroregeneration

Assessment of the Electronic Retinal Implant Alpha AMS in Restoring Vision to Blind Patients with End-Stage Retinitis Pigmentosa

Endogenous spartin (SPG20) is recruited to endosomes and lipid droplets and interacts with the ubiquitin E3 ligases AIP4 and AIP5

The Diagnostic Yield of Next Generation Sequencing in Inherited Retinal Diseases: A Systematic Review and Meta-analysis

Characterizing the Natural History of Visual Function in Choroideremia Using Microperimetry and Multimodal Retinal Imaging

Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners

Assessing the carbon footprint of fluorinated gases in vitreoretinal surgery

Female carriers of X-linked inherited retinal diseases – Genetics, diagnosis, and potential therapies

Gene therapy for inherited retinal diseases: progress and possibilities

The Spectrum of CHM Gene Mutations in Choroideremia and Their Relationship to Clinical Phenotype

The safety and efficacy of gene therapy treatment for monogenic retinal and optic nerve diseases: A systematic review

First-in-Human Robot-Assisted Subretinal Drug Delivery Under Local Anesthesia

Discovery of Māori and Polynesian phototransduction pathway founder mutation: what is the gene and what does it mean?

Perspectives of carriers of X-linked retinal diseases on genetic testing and gene therapy: A global survey

Correlation of Optical Coherence Tomography and Autofluorescence in the Outer Retina and Choroid of Patients With Choroideremia

Victorian evolution of inherited retinal diseases natural history registry (VENTURE study): Rationale, methodology and initial participant characteristics

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