Muddathir H. Hamad
Riyadh, Saudi Arabia
Last Updated: 09/26/2026
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Found 49 publications
Methodological Quality of Clinical Practice Guidelines for the Diagnosis of Simple Febrile Seizures in Children: A Systematic Review Using the Appraisal of Guidelines for Research and Evaluation II Instrument.
Journal: Pediatric neurology
Published: October 31, 2025
TTC19-related mitochondrial complex III deficiency: Clinical and genetic characterization of 10 patients from 5 unrelated Arab families.
Journal: Molecular genetics and metabolism
Published: October 07, 2025
TTC19-related mitochondrial complex III deficiency: Clinical and genetic characterization of 10 patients from 5 unrelated Arab families.
Journal: Molecular genetics and metabolism
Published: October 07, 2025
Vitamin D Supplementation for Children with Epilepsy on Antiseizure Medications: A Randomized Controlled Trial.
Journal: Children (Basel, Switzerland)
Published: August 14, 2024
The correlation of intracranial parenchymal calcium score and the severity of neurological clinical presentation in carbonic anhydrase deficiency type 2.
Journal: Brain & development
Published: August 08, 2024
Sodium Oxybate-Treated Familial Myoclonus-Dystonia Syndrome Due to Novel SGCE Variant.
Journal: American journal of medical genetics. Part A
Published: August 08, 2024
Virtual Objective Structured Clinical Examination (OSCE) Training in the Pandemic Era: Feasibility, Satisfaction, and the Road Ahead.
Journal: Cureus
Published: June 01, 2024
Case Report: A rare treatable metabolic syndrome (Brown-Vialetto-Van Laere syndrome) masquerading as chronic inflammatory demyelinating polyneuropathy from Saudi Arabia.
Journal: Frontiers in pediatrics
Published: January 31, 2024
Risk factors, clinical characteristics, and outcomes of perinatal stroke in a Tertiary University Hospital.
Journal: Neurosciences (Riyadh, Saudi Arabia)
Published: January 21, 2024
Case report: A late and isolated presentation of meningoencephalomyelitis uncovers a novel pathogenic variant in the CIITA gene.
Journal: Frontiers in pediatrics
Published: July 29, 2023
Corrigendum to: Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes.
Journal: Molecular genetics and metabolism
Published: July 15, 2023
Genotype-Phenotype Analysis of Children with Epilepsy Referred for Whole-Exome Sequencing at a Tertiary Care University Hospital.
Journal: Children (Basel, Switzerland)
Published: July 02, 2023
Last Updated: 09/26/2026