Wejdan S. Hakami
Riyadh, Saudi Arabia
Last Updated: 09/26/2026
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Found 11 publications
Case Report: Two siblings with a novel homozygous SLC18A2 variant causing parkinsonism-dystonia-2: a case series from Saudi Arabia.
Journal: Frontiers in genetics
Published: February 16, 2026
"Preventing vision loss in pediatric otogenic thrombosis: a case report highlighting surgical interventions".
Journal: Frontiers in ophthalmology
Published: October 30, 2025
National strategies for screening neural tube defects in Saudi Arabia: activating prevention and early intervention.
Journal: Frontiers in public health
Published: October 11, 2024
Elucidating the clinical and genetic spectrum of inositol polyphosphate phosphatase INPP4A-related neurodevelopmental disorder.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 18, 2023
Bi-allelic variants in HCRT cause autosomal recessive narcolepsy.
Journal: Neurogenetics
Published: November 28, 2023
Inherited Metabolic Causes of Stroke in Children: Mechanisms, Types, and Management.
Journal: Frontiers in neurology
Published: November 24, 2020
Spinal Cord Involvement in Pediatric-Onset Metabolic Disorders With Mendelian and Mitochondrial Inheritance.
Journal: Frontiers in pediatrics
Published: August 28, 2020
Metabolic and genetic disorders mimicking cerebral palsy.
Journal: Neurosciences (Riyadh, Saudi Arabia)
Published: August 06, 2019
The incidence and spectrum of central nervous system malformations in newborns over a decade (2001-2010) in the Central Region of Saudi Arabia.
Journal: Saudi medical journal
Published: November 08, 2011
Showing 1-11 of 11
Last Updated: 09/26/2026