Ali N. Alodaib
Riyadh, Saudi Arabia
Last Updated: 09/26/2026
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Found 8 publications
Case report: Clinical and genetic characterization of a novel ALDH7A1 variant causing pyridoxine-dependent epilepsy, developmental delay, and intellectual disability in two siblings.
Journal: Frontiers in psychiatry
Published: September 24, 2024
Role of age and sex in the incidence of adverse effects among diabetic patients treated with glipizide.
Journal: Experimental and therapeutic medicine
Published: May 27, 2024
Clinical, radiological, and genetic characterization of SLC13A5 variants in Saudi families: Genotype phenotype correlation and brief review of the literature.
Journal: Frontiers in pediatrics
Published: September 22, 2022
Incidence of newborn screening disorders among 56632 infants in Central Saudi Arabia. A 6-year study.
Journal: Saudi medical journal
Published: July 01, 2020
First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient.
Journal: Molecular cytogenetics
Published: February 13, 2019
The Prevalence of Phenylketonuria in Arab Countries, Turkey, and Iran: A Systematic Review.
Journal: BioMed research international
Published: December 18, 2017
A Novel Homozygous Mutation in SPTBN2 Leads to Spinocerebellar Ataxia in a Consanguineous Family: Report of a New Infantile-Onset Case and Brief Review of the Literature.
Journal: Cerebellum (London, England)
Published: December 03, 2017
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Last Updated: 09/26/2026