Enam Y. Danish
Jeddah, Saudi Arabia
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy.
Journal: Cureus
Published: April 06, 2026
POC1B-associated cone-rod dystrophy with bilateral optic disc swelling: A novel clinical observation.
Journal: American journal of ophthalmology case reports
Published: May 03, 2025
Adult genomic medicine: lessons from a multisite study of 2700 patients.
Journal: Genome medicine
Published: April 24, 2025
Incidence and risk factors of ocular complications among patients with homocystinuria in Saudi Arabia: a cross-sectional study.
Journal: Annals of medicine and surgery (2012)
Published: October 04, 2024
Mutations in the ciliary transport gene IFT140 cause syndromic congenital retinal dystrophy.
Journal: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus
Published: March 11, 2024
Refractive Changes among Diode Laser-treated Retinopathy of Prematurity Patients: A Retrospective Study.
Journal: Middle East African journal of ophthalmology
Published: August 12, 2023
Phenotype and genotype of 15 Saudi patients with achromatopsia: A case series.
Journal: Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society
Published: May 15, 2023
Relationship Between Screen Time and Dry Eye Symptoms During the COVID-19 Pandemic in the Pediatric Population of the Western Region of Saudi Arabia.
Journal: Cureus
Published: November 02, 2022
Effects of Early Treatment of Retinopathy of Prematurity at a Tertiary Care Hospital in Saudi Arabia: A Retrospective Study.
Journal: Journal of pediatric ophthalmology and strabismus
Published: July 21, 2021
Biallelic variants in SLC38A3 encoding a glutamine transporter cause epileptic encephalopathy.
Journal: Brain : a journal of neurology
Published: March 17, 2021
Showing 1-10 of 10
Last Updated: 09/26/2026