Jonathan Aboshiha

London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 16 publications

Long-Term Investigation of Retinal Function in Patients with Achromatopsia.

Long-Term Investigation of Retinal Function in Patients with Achromatopsia.

Journal: Investigative ophthalmology & visual science

Published: September 22, 2020

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

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

Journal: Investigative ophthalmology & visual science

Published: December 05, 2018

Differential Survival of Penetrating and Lamellar Transplants in Management of Failed Corneal Grafts.

Differential Survival of Penetrating and Lamellar Transplants in Management of Failed Corneal Grafts.

Journal: JAMA ophthalmology

Published: June 23, 2018

Cross-Sectional and Longitudinal Assessment of Retinal Sensitivity in Patients With Childhood-Onset Stargardt Disease.

Cross-Sectional and Longitudinal Assessment of Retinal Sensitivity in Patients With Childhood-Onset Stargardt Disease.

Journal: Translational vision science & technology

Published: January 09, 2018

Achromatopsia: clinical features, molecular genetics, animal models and therapeutic options.

Achromatopsia: clinical features, molecular genetics, animal models and therapeutic options.

Journal: Ophthalmic genetics

Published: January 06, 2018

A Quantitative and Qualitative Exploration of Photoaversion in Achromatopsia.

A Quantitative and Qualitative Exploration of Photoaversion in Achromatopsia.

Journal: Investigative ophthalmology & visual science

Published: July 18, 2017

Dissociations in Coherence Sensitivity Reveal Atypical Development of Cortical Visual Processing in Congenital Achromatopsia.

Dissociations in Coherence Sensitivity Reveal Atypical Development of Cortical Visual Processing in Congenital Achromatopsia.

Journal: Investigative ophthalmology & visual science

Published: April 29, 2016

Investigation of Aberrant Splicing Induced by AIPL1 Variations as a Cause of Leber Congenital Amaurosis.

Investigation of Aberrant Splicing Induced by AIPL1 Variations as a Cause of Leber Congenital Amaurosis.

Journal: Investigative ophthalmology & visual science

Published: December 10, 2015

The cone dysfunction syndromes.

The cone dysfunction syndromes.

Journal: The British journal of ophthalmology

Published: December 08, 2014

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

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

Journal: Investigative ophthalmology & visual science

Published: October 04, 2014

Preserved outer retina in AIPL1 Leber's congenital amaurosis: implications for gene therapy.

Preserved outer retina in AIPL1 Leber's congenital amaurosis: implications for gene therapy.

Journal: Ophthalmology

Published: September 24, 2014

Dark-adaptation functions in molecularly confirmed achromatopsia and the implications for assessment in retinal therapy trials.

Dark-adaptation functions in molecularly confirmed achromatopsia and the implications for assessment in retinal therapy trials.

Journal: Investigative ophthalmology & visual science

Published: August 30, 2014

Showing 1-12 of 16

Last Updated: 09/26/2026