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List of works by Neruban Kumaran

A Cross-Sectional and Longitudinal Study of Retinal Sensitivity in RPE65-Associated Leber Congenital Amaurosis

scientific article published on 01 July 2018

A NOVEL CASE SERIES OF NMNAT1-ASSOCIATED EARLY-ONSET RETINAL DYSTROPHY: EXTENDING THE PHENOTYPIC SPECTRUM

scientific article published on 11 July 2018

A Quantitative and Qualitative Exploration of Photoaversion in Achromatopsia.

scientific article

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

scientific article published on 01 January 2019

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

Cross-Sectional and Longitudinal Assessment of the Ellipsoid Zone in Childhood-Onset Stargardt Disease

Detailed clinical characterisation, unique features and natural history of autosomal recessive RDH12-associated retinal degeneration

scientific article published on 12 April 2019

Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy Overview

scientific article published on 5 October 2018

Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies

scientific article published on 2 February 2018

Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions

scientific article

Long-Term Investigation of Retinal Function in Patients with Achromatopsia

scientific article published on 01 September 2020

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

Retinal Structure in RPE65-Associated Retinal Dystrophy

scientific article published on 01 April 2020

Retinal gene therapy

scientific article published on 01 June 2018

Severe Loss of Tritan Color Discrimination in RPE65 Associated Leber Congenital Amaurosis

scientific article published in January 2018

The integrity and organization of the human AIPL1 functional domains is critical for its role as a HSP90-dependent co-chaperone for rod PDE6.

scientific article published on 26 August 2017

The integrity and organization of the human AIPL1 functional domains is critical for its role as a HSP90-dependent co-chaperone for rod PDE6.

scientific article published on 16 January 2018

Validation of a Vision-Guided Mobility Assessment for RPE65-Associated Retinal Dystrophy

scientific article published on 03 September 2020

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