Leen Safieh-Abu
Al Oroubah St
Riyadh, Saudi Arabia
Riyadh, Saudi Arabia
Last Updated: 09/26/2026
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Found 25 publications
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
Advanced coats-like retinopathy as the initial presentation of Familial Retinal Arterial Macroaneurysms.
Journal: American journal of ophthalmology case reports
Published: May 02, 2017
Benign reactive lymphoid hyperplasia of the conjunctiva in childhood.
Journal: The British journal of ophthalmology
Published: May 11, 2016
Novel Mutations in Two Saudi Patients with Congenital Retinal Dystrophy.
Journal: Middle East African journal of ophthalmology
Published: March 10, 2016
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.
Journal: Nature genetics
Published: August 08, 2014
Retinal reactive astrocytic tumor: gene expression profiling.
Journal: JAMA ophthalmology
Published: June 13, 2014
Rod-Cone Dystrophy with Initially Preserved Visual Acuity Despite Early Macular Involvement Suggests Recessive CERKL Mutations.
Journal: Ophthalmic genetics
Published: February 20, 2014
Childhood cone-rod dystrophy with macular cystic degeneration from recessive CRB1 mutation.
Journal: Ophthalmic genetics
Published: June 18, 2013
The RPGRIP1-related retinal phenotype in children.
Journal: The British journal of ophthalmology
Published: March 19, 2013
Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes.
Journal: Genome research
Published: October 30, 2012
Molecular characterization of Joubert syndrome in Saudi Arabia.
Journal: Human mutation
Published: April 14, 2012
Last Updated: 09/26/2026