Tarek I. Omar
Alexandria, ALX, Egypt
Last Updated: 09/26/2026
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Found 21 publications
Bi-allelic variants in NRDC cause a neurodevelopmental disorder characterized by neonatal lethality, microcephaly, and brain abnormalities.
Journal: American journal of human genetics
Published: July 19, 2025
MDGA2 homozygous loss-of-function variants cause developmental and epileptic encephalopathy.
Journal: American journal of human genetics
Published: July 14, 2025
Response to Letter to the Editor Regarding the Article: Effectiveness of Virtual Reality Glasses Versus White Noise on Dental Anxiety in Children With Attention-Deficit/Hyperactivity Disorder: A Randomised Controlled Clinical Trial.
Journal: International journal of paediatric dentistry
Published: February 21, 2025
Egyptian pediatric guidelines for the management of childhood venous thromboembolism: the adapted methodology: a limited resource country perspective.
Journal: Thrombosis journal
Published: January 04, 2025
Corrigendum to "Adapted Evidence-Based Clinical Practice Guidelines for Diagnosis and Treatment of Epilepsies in Children: A Tertiary Children's Hospital Update" Pediatric Neurology 141C (2023) (87-92).
Journal: Pediatric neurology
Published: February 22, 2024
Effectiveness of virtual reality glasses versus white noise on dental anxiety in children with attention-deficit hyperactivity disorder: A randomised controlled clinical trial.
Journal: International journal of paediatric dentistry
Published: February 15, 2024
Egyptian Pediatric Guidelines for the Management of Children with Isolated Thrombocytopenia Using the Adapted ADAPTE Methodology-A Limited-Resource Country Perspective.
Journal: Children (Basel, Switzerland)
Published: February 09, 2024
Transfusion of blood components in pediatric age groups: an evidence-based clinical practice guideline adapted for the use in Egypt using 'Adapted ADAPTE'.
Journal: Annals of hematology
Published: November 24, 2023
Adapting global evidence-based practice guidelines to the Egyptian healthcare context: the Egyptian Pediatric Clinical Practice Guidelines Committee (EPG) initiative.
Journal: Bulletin of the National Research Centre
Published: April 25, 2023
Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome-1 in two new patients with the same homozygous TMCO1 variant and review of the literature.
Journal: European journal of medical genetics
Published: October 26, 2022
Last Updated: 09/26/2026