Waseem M. Fathalla

Abu Dhabi, AZ, United Arab Emirates

Last Updated: 09/26/2026

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Found 14 publications

Pediatric Stroke in a United Arab Emirates (UAE) Tertiary Care Center: A Retrospective Descriptive Study.

Pediatric Stroke in a United Arab Emirates (UAE) Tertiary Care Center: A Retrospective Descriptive Study.

Journal: Cureus
Published: October 25, 2025

Bilateral Ptosis, Diplopia, and Vertical Gaze Palsy: An Unusual Presentation of Adolescent Aquaporin-4 (AQP4)-Antibody Positive Neuromyelitis Optica Spectrum Disorder.

Bilateral Ptosis, Diplopia, and Vertical Gaze Palsy: An Unusual Presentation of Adolescent Aquaporin-4 (AQP4)-Antibody Positive Neuromyelitis Optica Spectrum Disorder.

Journal: Cureus
Published: September 11, 2025

Genotype-Phenotype Correlation and Therapeutic Amenability in a Cohort of Rett Syndrome Patients: A Single-Center Study.

Genotype-Phenotype Correlation and Therapeutic Amenability in a Cohort of Rett Syndrome Patients: A Single-Center Study.

Journal: Cureus
Published: June 28, 2025

A Case of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Optic Neuritis Responsive to Intravenous Immunoglobulin (IVIG) Therapy in a Pediatric Patient.

A Case of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Optic Neuritis Responsive to Intravenous Immunoglobulin (IVIG) Therapy in a Pediatric Patient.

Journal: Cureus
Published: August 09, 2023

Anti-U1RNP-70kD-positive case of neonatal lupus presenting with seizure and incomplete heart block: a case report and literature review.

Anti-U1RNP-70kD-positive case of neonatal lupus presenting with seizure and incomplete heart block: a case report and literature review.

Journal: Frontiers in pediatrics
Published: June 13, 2023

Gene Therapy for Duchenne Muscular Dystrophy: Unlocking the Opportunities in Countries in the Middle East and Beyond.

Gene Therapy for Duchenne Muscular Dystrophy: Unlocking the Opportunities in Countries in the Middle East and Beyond.

Journal: Journal of neuromuscular diseases
Published: October 17, 2022

Linear Nevus Sebaceous Syndrome in a Child With Infantile Spasms and Focal Cortical Dysplasia.

Linear Nevus Sebaceous Syndrome in a Child With Infantile Spasms and Focal Cortical Dysplasia.

Journal: Cureus
Published: September 03, 2021

De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy.

De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy.

Journal: Molecular brain
Published: June 29, 2021

Characterization of ETFDH and PHGDH Mutations in a Patient with Mild Glutaric Aciduria Type II and Serine Deficiency.

Characterization of ETFDH and PHGDH Mutations in a Patient with Mild Glutaric Aciduria Type II and Serine Deficiency.

Journal: Genes
Published: April 11, 2021

Current management of Duchenne muscular dystrophy in the Middle East: expert report.

Current management of Duchenne muscular dystrophy in the Middle East: expert report.

Journal: Neurodegenerative disease management
Published: June 06, 2019

International working group identifies need for newborn screening for mucopolysaccharidosis type I but states that existing hurdles must be overcome.

International working group identifies need for newborn screening for mucopolysaccharidosis type I but states that existing hurdles must be overcome.

Journal: Acta paediatrica (Oslo, Norway : 1992)
Published: April 12, 2018

Easy-to-use algorithm would provide faster diagnoses for mucopolysaccharidosis type I and enable patients to receive earlier treatment.

Easy-to-use algorithm would provide faster diagnoses for mucopolysaccharidosis type I and enable patients to receive earlier treatment.

Journal: Acta paediatrica (Oslo, Norway : 1992)
Published: February 16, 2018
Showing 1-12 of 14

Last Updated: 09/26/2026