Mohammed F. Aljabri
Ta'if, Saudi Arabia
Last Updated: 09/26/2026
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Found 8 publications
Vertebral artery dissection aneurysm in a pediatric patient: A rare case with unusual clinical manifestations, diagnostic, and management challenges.
Journal: Medicine
Published: November 28, 2023
Pediatric myelin oligodendrocyte glycoprotein antibody associated disease-Asymmetric papilledema and elevated ICP are two of the chameleons: A case report.
Journal: Medicine
Published: February 24, 2023
"Progressive myoclonic ataxia and developmental/epileptic encephalopathy associated with a novel homozygous mutation in TCN2 gene".
Journal: Molecular genetics & genomic medicine
Published: February 04, 2023
Developmental and/or epileptic encephalopathy with spike-and-wave activation in sleep in Saudi Arabia: Electroclinical, etiologic, genetic, and outcome multicenter study.
Journal: Seizure
Published: January 12, 2023
An Unusual Case of Headache in a Child: Idiopathic Intracranial Hypertension with Diagnostic Challenge.
Journal: Clinical medicine insights. Case reports
Published: December 09, 2022
Favorable response to carbamazepine therapy in genetically proven myoclonus-dystonia child.
Journal: Italian journal of pediatrics
Published: July 30, 2020
First report of co-morbidity of pantothenate kinase-associated neurodegeneration and three types of chronic hemolytic anemias.
Journal: Annals of medicine and surgery (2012)
Published: March 27, 2015
Showing 1-8 of 8
Last Updated: 09/26/2026