Search Results - "Rosa, Potyra R"
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Initial results from a first-in-human gene therapy trial on X-linked retinitis pigmentosa caused by mutations in RPGR
Published in Nature medicine (01-03-2020)“…Retinal gene therapy has shown great promise in treating retinitis pigmentosa (RP), a primary photoreceptor degeneration that leads to severe sight loss in…”
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Choroideremia Gene Therapy Phase 2 Clinical Trial: 24-Month Results
Published in American journal of ophthalmology (01-01-2019)“…To report the final results of a phase 2 high-dose gene therapy clinical trial in choroideremia. Design: Phase 2 clinical trial. Participants: Six men (aged…”
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Differentiating Mild Papilledema and Buried Optic Nerve Head Drusen Using Spectral Domain Optical Coherence Tomography
Published in Ophthalmology (Rochester, Minn.) (01-04-2014)“…Purpose To evaluate the clinical utility of spectral domain optical coherence tomography (SD-OCT) in differentiating mild papilledema from buried optic nerve…”
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Characteristics and Surgical Outcomes of Comitant Esotropia in an Adult Population Between 18 and 60 Years Old
Published in American journal of ophthalmology (01-11-2024)“…To describe the clinical characteristics and surgical outcomes of adults with comitant nonaccommodative esotropia. Retrospective case series. Retrospective…”
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Choroidal Thickness in Eyes With Central Geographic Atrophy Secondary to Stargardt Disease and Age-Related Macular Degeneration
Published in Ophthalmic surgery, lasers & imaging retina (01-09-2015)“…Choroidal thickness (CT) measurements from eyes with similar areas of macular geographic atrophy (GA) secondary to age-related macular degeneration (AMD) and…”
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Trial end points and natural history in patients with G11778A Leber hereditary optic neuropathy : preparation for gene therapy clinical trial
Published in JAMA ophthalmology (01-04-2014)“…IMPORTANCE Establishing the natural history of G11778A Leber hereditary optic neuropathy (LHON) is important to determine the optimal end points to assess the…”
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Retinal ganglion cell dysfunction in asymptomatic G11778A: Leber hereditary optic neuropathy
Published in Investigative ophthalmology & visual science (10-02-2014)“…To report the serial evaluation of asymptomatic eyes of subjects with mutated G11778A mitochondrial DNA. Forty-five asymptomatic G11778A Leber hereditary optic…”
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Relationship Between Optic Nerve Protrusion Measured by OCT and MRI and Papilledema Severity
Published in Investigative ophthalmology & visual science (01-04-2015)“…To develop measures of optic nerve protrusion length (NPL) from optical coherence tomography (OCT) and magnetic resonance imagining (MRI) and compare these…”
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Analysis of Socioeconomic Factors Affecting Follow-Up in a Glaucoma Screening Program
Published in Clinical ophthalmology (Auckland, N.Z.) (01-01-2021)“…To determine what socioeconomic factors affect follow-up in a glaucoma screening program. This was a retrospective cohort study of six health fairs in South…”
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Macular Retinal Sublayer Thicknesses in G11778A Leber Hereditary Optic Neuropathy
Published in Ophthalmic surgery, lasers & imaging retina (01-09-2016)“…To determine macular retinal sublayer thickness changes in G11778A Leber hereditary optic neuropathy (LHON). The authors performed a cross-sectional study by…”
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Ventriculoperitoneal Shunt as a Treatment of Visual Loss in Idiopathic Intracranial Hypertension
Published in Journal of neuro-ophthalmology (01-09-2014)“…BACKGROUND:The aims of this study were to evaluate visual function outcomes in idiopathic intracranial hypertension (IIH) patients who underwent…”
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Dilated eye examination screening guideline compliance among patients with diabetes without a diabetic retinopathy diagnosis: the role of geographic access
Published in BMJ open diabetes research & care (2014)“…Objective To estimate the prevalence of, and factors associated with, dilated eye examination guideline compliance among patients with diabetes mellitus (DM),…”
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Changes in Retinal Sensitivity Associated With Cotoretigene Toliparvovec in X-Linked Retinitis Pigmentosa With RPGR Gene Variations
Published in JAMA ophthalmology (01-03-2023)“…X-linked retinitis pigmentosa (XLRP) is a severe cause of early-onset RP in male individuals, characterized by degeneration of photoreceptors, an extinguished…”
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Quality of life in idiopathic intracranial hypertension at diagnosis: IIH Treatment Trial results
Published in Neurology (16-06-2015)“…OBJECTIVE:The study purpose was to examine vision-specific and overall health-related quality of life (QOL) at baseline in Idiopathic Intracranial Hypertension…”
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Risk factors for poor visual outcome in patients with idiopathic intracranial hypertension
Published in Neurology (01-09-2015)“…OBJECTIVES:Determine potential risk factors for progressive visual field loss in the Idiopathic Intracranial Hypertension Treatment Trial, a randomized…”
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Retinal gene therapy in X-linked retinitis pigmentosa caused by mutations in RPGR: Results at 6 months in a first in human clinical trial
Published in Nature medicine (24-02-2020)“…Retinal gene therapy has shown great promise in treating retinitis pigmentosa (RP), a primary photoreceptor degeneration that leads to severe sight loss in…”
Get full text
Journal Article