Ali D. Otaibi-Al
Riyadh, Saudi Arabia
Last Updated: 09/26/2026
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Found 12 publications
Exploring the clinical, neuroimaging, and genetic spectrum of PLPBP deficiency: multicenter case series and systematic review.
Journal: Molecular genetics and metabolism
Published: September 22, 2025
Stiripentol safety profile and efficacy in cases of SCN1A-related Dravet syndrome, multi-center experience, Saudi Arabia.
Journal: Neurosciences (Riyadh, Saudi Arabia)
Published: February 26, 2024
Diagnosis and management of infantile epileptic spasms syndrome (IESS) in Gulf Cooperation Council (GCC) countries: Expert consensus statement.
Journal: Seizure
Published: December 06, 2023
Developmental and/or epileptic encephalopathy with spike-and-wave activation in sleep in Saudi Arabia: Electroclinical, etiologic, genetic, and outcome multicenter study.
Journal: Seizure
Published: January 12, 2023
Clinical and Molecular Characteristics of Neuronal Ceroid Lipofuscinosis in Saudi Arabia.
Journal: Pediatric neurology
Published: October 04, 2022
El-Hattab-Alkuraya syndrome caused by biallelic WDR45B pathogenic variants: Further delineation of the phenotype and genotype.
Journal: Clinical genetics
Published: February 10, 2022
Seizure-related injuries in people with epilepsy: A cohort study from Saudi Arabia.
Journal: Epilepsia open
Published: January 26, 2022
Uridine monophosphate (UMP)-responsive developmental and epileptic encephalopathy: A case report of two siblings and a review of literature.
Journal: Molecular genetics and metabolism reports
Published: October 29, 2021
Efficacy and safety of corpus callosotomy versus vagus nerve stimulation as long-term adjunctive therapies in children with Lennox-Gastaut syndrome: Experience of a tertiary care center.
Journal: Neurosciences (Riyadh, Saudi Arabia)
Published: October 24, 2021
Cell-based analysis of CAD variants identifies individuals likely to benefit from uridine therapy.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 11, 2020
Bi-allelic Variants in IQSEC1 Cause Intellectual Disability, Developmental Delay, and Short Stature.
Bi-allelic Variants in IQSEC1 Cause Intellectual Disability, Developmental Delay, and Short Stature.
Journal: American journal of human genetics
Published: July 01, 2019
Showing 1-12 of 12
Last Updated: 09/26/2026