Assessing the Interocular Symmetry of Foveal Outer Nuclear Layer Thickness in Achromatopsia (Q90643989)

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15 April 2020

title

Assessing the Interocular Symmetry of Foveal Outer Nuclear Layer Thickness in Achromatopsia (English)

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15 April 2020

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Rebecca R Mastey

1

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15 April 2020

Mina Gaffney

2

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15 April 2020

Katie M Litts

3

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15 April 2020

Christopher S Langlo

4

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15 April 2020

Emily J Patterson

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Margaret R Strampe

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Angelos Kalitzeos

7

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15 April 2020

Michel Michaelides

8

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15 April 2020

Joseph Carroll

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15 April 2020

publication date

1 September 2019

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Translational vision science & technology

15 April 2020

published in

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volume

8

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issue

5

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page(s)

21

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Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International

15 April 2020

copyright license

start time

2 October 2019

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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12 December 2020

Measuring agreement in method comparison studies

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Swelling and loss of photoreceptors in chronic human and experimental glaucomas

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Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsia

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CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia

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A pyramid approach to subpixel registration based on intensity

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Genetic etiology and clinical consequences of complete and incomplete achromatopsia.

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Gene therapy rescues cone function in congenital achromatopsia

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Progressive loss of cones in achromatopsia: an imaging study using spectral-domain optical coherence tomography.

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Long-term and age-dependent restoration of visual function in a mouse model of CNGB3-associated achromatopsia following gene therapy

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A nonsense mutation in PDE6H causes autosomal-recessive incomplete achromatopsia

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Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement

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Proposed lexicon for anatomic landmarks in normal posterior segment spectral-domain optical coherence tomography: the IN•OCT consensus.

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In vivo imaging of human cone photoreceptor inner segments.

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A prospective longitudinal study of retinal structure and function in achromatopsia.

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Genotype-dependent variability in residual cone structure in achromatopsia: toward developing metrics for assessing cone health

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Inner Segment Remodeling and Mitochondrial Translocation in Cone Photoreceptors in Age-Related Macular Degeneration With Outer Retinal Tubulation.

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The cone dysfunction syndromes

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Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia

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12 December 2020

Gene Augmentation Therapy Restores Retinal Function and Visual Behavior in a Sheep Model of CNGA3 Achromatopsia

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12 December 2020

Evaluating the effect of pupil dilation on spectral-domain optical coherence tomography measurements and their quality score

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12 December 2020

Directional Optical Coherence Tomography Reveals Reliable Outer Nuclear Layer Measurements

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12 December 2020

Residual Foveal Cone Structure in CNGB3-Associated Achromatopsia

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12 December 2020

Necrotic enlargement of cone photoreceptor cells and the release of high-mobility group box-1 in retinitis pigmentosa

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12 December 2020

Effect of age and sex on retinal layer thickness and volume in normal eyes

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12 December 2020

Evaluating outer segment length as a surrogate measure of peak foveal cone density

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12 December 2020

REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA.

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12 December 2020

The Clinical Phenotype of CNGA3-Related Achromatopsia: Pretreatment Characterization in Preparation of a Gene Replacement Therapy Trial.

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Retinal Cyclic Nucleotide-Gated Channels: From Pathophysiology to Therapy.

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Impacts of age and sex on retinal layer thicknesses measured by spectral domain optical coherence tomography with Spectralis.

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Longitudinal Assessment of Retinal Structure in Achromatopsia Patients With Long-Term Follow-up

1 reference

12 December 2020

Adaptive Optics Retinal Imaging in CNGA3-Associated Achromatopsia: Retinal Characterization, Interocular Symmetry, and Intrafamilial Variability

1 reference

12 December 2020

Identifiers

DOI

10.1167/TVST.8.5.21

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31602346 AND SRC:MED&resulttype=core&format=json

15 April 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31602346 AND SRC:MED&resulttype=core&format=json

15 April 2020

PubMed publication ID

31602346

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