Ehab R. Abdelraouf
Cairo, C, Egypt
Last Updated: 09/26/2026
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Found 13 publications
Clinical Utility of Genetic Diagnosis in Drug-Resistant Epilepsy: Refining Classification and Guiding Therapy in an Egyptian Cohort.
Journal: Clinical genetics
Published: November 20, 2025
Mapping autism in Egypt: population-based insights into prevalence, risk determinants, and severity among children aged 1-12 years.
Journal: Molecular autism
Published: December 09, 2024
BDNF, proBDNF and proBDNF/BDNF ratio with electroencephalographic abnormalities in children with attention deficit hyperactivity disorder: Possible relations to cognition and severity.
Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
Published: December 13, 2023
Childhood Apraxia of Speech: Exploring Gluten Sensitivity and Changes in Glutamate and Gamma-Aminobutyric Acid Plasma Levels.
Journal: Pediatric neurology
Published: July 07, 2023
BDNF Val66Met Polymorphism: Suggested Genetic Involvement in Some Children with Learning Disorder.
Journal: Journal of molecular neuroscience : MN
Published: August 13, 2022
Kynurenine and oxidative stress in children having learning disorder with and without attention deficit hyperactivity disorder: possible role and involvement.
Journal: BMC neurology
Published: April 24, 2022
Asymmetry Matters: Diffusion Tensor Tractography of the Uncinate Fasciculus in Children with Verbal Memory Deficits.
Journal: AJNR. American journal of neuroradiology
Published: January 22, 2022
Correlation between diffusion tensor imaging measures and the reading and cognitive performance of Arabic readers: dyslexic children perspective.
Journal: Neuroradiology
Published: September 22, 2019
Investigating the influence of ubiquinone blood level on the abilities of children with specific learning disorder.
Journal: The Egyptian journal of neurology, psychiatry and neurosurgery
Published: March 05, 2018
Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental Disorders.
Journal: JAMA psychiatry
Published: January 18, 2017
Johnson-McMillin Microtia Syndrome: New Additional Family.
Journal: Journal of family medicine and primary care
Published: November 07, 2014
Last Updated: 09/26/2026