Ehab Abdelkader

Corsebar Rd
Paisley, SCT, United Kingdom

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 14 publications

Analysis of retinal structure and function in cone dystrophy with supernormal rod response.

Analysis of retinal structure and function in cone dystrophy with supernormal rod response.

Journal: Documenta ophthalmologica. Advances in ophthalmology

Published: June 15, 2019

Non-syndromic retinal dystrophy associated with homozygous mutations in the ALMS1 gene.

Non-syndromic retinal dystrophy associated with homozygous mutations in the ALMS1 gene.

Journal: Ophthalmic genetics

Published: November 30, 2018

Severe retinitis pigmentosa phenotype associated with novel CNGB1 variants.

Severe retinitis pigmentosa phenotype associated with novel CNGB1 variants.

Journal: American journal of ophthalmology case reports

Published: November 04, 2018

Nd:YAG laser therapy for non-resolving premacular subhyaloid hemorrhage in Saudi patients.

Nd:YAG laser therapy for non-resolving premacular subhyaloid hemorrhage in Saudi patients.

Journal: Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society

Published: October 13, 2018

Novel causative variants in patients with achromatopsia.

Novel causative variants in patients with achromatopsia.

Journal: Ophthalmic genetics

Published: October 06, 2018

Congenital stationary night blindness associated with morning glory disc malformation: a novel hemizygous mutation in CACNA1F.

Congenital stationary night blindness associated with morning glory disc malformation: a novel hemizygous mutation in CACNA1F.

Journal: Ophthalmic genetics

Published: August 02, 2018

DIFFUSE RETINAL VASCULAR LEAKAGE AND CONE-ROD DYSTROPHY IN A FAMILY WITH THE HOMOZYGOUS MISSENSE C.1429G>A (P.GLY477ARG) MUTATION IN CRB1.

DIFFUSE RETINAL VASCULAR LEAKAGE AND CONE-ROD DYSTROPHY IN A FAMILY WITH THE HOMOZYGOUS MISSENSE C.1429G>A (P.GLY477ARG) MUTATION IN CRB1.

Journal: Retinal cases & brief reports

Published: December 05, 2017

A Case of Unilateral Retinitis Pigmentosa Associated with Full Thickness Macular Hole.

A Case of Unilateral Retinitis Pigmentosa Associated with Full Thickness Macular Hole.

Journal: Middle East African journal of ophthalmology

Published: September 23, 2017

Severe retinal degeneration at an early age in Usher syndrome type 1B associated with homozygous splice site mutations in MYO7A gene.

Severe retinal degeneration at an early age in Usher syndrome type 1B associated with homozygous splice site mutations in MYO7A gene.

Journal: Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society

Published: September 09, 2017

Serous retinal detachment after panretinal photocoagulation for proliferative diabetic retinopathy: a case report.

Serous retinal detachment after panretinal photocoagulation for proliferative diabetic retinopathy: a case report.

Journal: Journal of medical case reports

Published: November 28, 2016

Pneumatic displacement of submacular haemorrhage.

Pneumatic displacement of submacular haemorrhage.

Journal: Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society

Published: May 05, 2016

Accidental macular injury with class IVb laser outside the medical settings.

Accidental macular injury with class IVb laser outside the medical settings.

Journal: Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society

Published: March 14, 2016

Showing 1-12 of 14

Last Updated: 09/26/2026