Normal central retinal function and structure preserved in retinitis pigmentosa. - Wikidata - awgldk - TriplyDB

Normal central retinal function and structure preserved in retinitis pigmentosa.

Normal central retinal function and structure preserved in retinitis pigmentosa.

http://www.wikidata.org/entity/Q39942382

about

Structure-function correlation of the human central retina Biophysical Properties of Optogenetic Tools and Their Application for Vision Restoration Approaches Macular function in macular degenerations: repeatability of microperimetry as a potential outcome measure for ABCA4-associated retinopathy trials.VFMA: Topographic Analysis of Sensitivity Data From Full-Field Static Perimetry A comparison of visual field sensitivity to photoreceptor thickness in retinitis pigmentosa.Topical isopropyl unoprostone for retinitis pigmentosa: microperimetric results of the phase 2 clinical study Optogenetic therapy for retinitis pigmentosa.The transition zone between healthy and diseased retina in patients with retinitis pigmentosa Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations.Correlation of outer nuclear layer thickness with cone density values in patients with retinitis pigmentosa and healthy subjects.Rod sensitivity, cone sensitivity, and photoreceptor layer thickness in retinal degenerative diseases.Vision test variability in retinitis pigmentosa and psychosocial factors.Autofluorescence imaging with near-infrared excitation:normalization by reflectance to reduce signal from choroidal fluorophores.Retinal disease course in Usher syndrome 1B due to MYO7A mutations Correlation of structure and function of the macula in patients with retinitis pigmentosa Relationships among multifocal electroretinogram amplitude, visual field sensitivity, and SD-OCT receptor layer thicknesses in patients with retinitis pigmentosa Gene therapy for retinitis pigmentosa caused by MFRP mutations: human phenotype and preliminary proof of concept.Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies.TULP1 mutations causing early-onset retinal degeneration: preserved but insensitive macular cones.Contrast visual acuity in patients with retinitis pigmentosa assessed by a contrast sensitivity tester.Structure-Function Modeling of Optical Coherence Tomography and Standard Automated Perimetry in the Retina of Patients with Autosomal Dominant Retinitis Pigmentosa Preservation of cone photoreceptors after a rapid yet transient degeneration and remodeling in cone-only Nrl-/- mouse retina Determining consequences of retinal membrane guanylyl cyclase (RetGC1) deficiency in human Leber congenital amaurosis en route to therapy: residual cone-photoreceptor vision correlates with biochemical properties of the mutants Decreased retinal-choroidal blood flow in retinitis pigmentosa as measured by MRI.Association between multifocal electroretinograms, optical coherence tomography and central visual sensitivity in advanced retinitis pigmentosa.Primary visual cortical remapping in patients with inherited peripheral retinal degeneration.Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.AAV-mediated Gene Therapy Halts Retinal Degeneration in PDE6β-deficient Dogs.SPATA7: Evolving phenotype from cone-rod dystrophy to retinitis pigmentosa Whole exome sequencing identified novel CRB1 mutations in Chinese and Indian populations with autosomal recessive retinitis pigmentosa.Optical Coherence Tomography of Retinal Degeneration in Royal College of Surgeons Rats and Its Correlation with Morphology and Electroretinography Progressive constriction of the hyperautofluorescent ring in retinitis pigmentosa.The structure-function relationship measured with optical coherence tomography and a microperimeter with auto-tracking: the MP-3, in patients with retinitis pigmentosa.Characterization of photoreceptor degeneration in the rhodopsin P23H transgenic rat line 2 using optical coherence tomography.

P2860

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P2860

Normal central retinal function and structure preserved in retinitis pigmentosa.

http://www.wikidata.org/entity/Q39942382

description

2009 nî lūn-bûn

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2009年の論文

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2009年論文

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2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

2009年论文

@zh

2009年论文

@zh-cn

name

Normal central retinal function and structure preserved in retinitis pigmentosa.

@en

Normal central retinal function and structure preserved in retinitis pigmentosa.

@nl

type

label

Normal central retinal function and structure preserved in retinitis pigmentosa.

@en

Normal central retinal function and structure preserved in retinitis pigmentosa.

@nl

prefLabel

Normal central retinal function and structure preserved in retinitis pigmentosa.

@en

Normal central retinal function and structure preserved in retinitis pigmentosa.

@nl

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P1433

Investigative Ophthalmology & Visual Science

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Normal central retinal function and structure preserved in retinitis pigmentosa

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P2093

Alejandro J Roman

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Alexander Sumaroka

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Artur V Cideciyan

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Elizabeth A M Windsor

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Janet D Steinberg

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Lori A Atkinson

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Sharon B Schwartz

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Tomas S Aleman

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1079-1085

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scholarly article

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10.1167/IOVS.09-4372

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2

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51

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Samuel G. Jacobson

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2009-09-24T00:00:00Z

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19797198

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