Montaha Almudhry

Dammam, Saudi Arabia

Last Updated: 09/26/2026

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Found 12 publications

Perceptions of pediatric neurologists on the ideal candidate: a nationwide survey.

Perceptions of pediatric neurologists on the ideal candidate: a nationwide survey.

Journal: BMC medical education

Published: January 06, 2026

A potential explanation of the pathophysiology of vigabatrin-associated brain abnormalities on MRI.

A potential explanation of the pathophysiology of vigabatrin-associated brain abnormalities on MRI.

Journal: Pediatric research

Published: July 27, 2025

Outcome of two siblings with late-onset Krabbe disease following allogeneic hematopoietic stem cell transplantation: And review of literature.

Outcome of two siblings with late-onset Krabbe disease following allogeneic hematopoietic stem cell transplantation: And review of literature.

Journal: Molecular genetics and metabolism reports

Published: February 13, 2025

Brain Volumes in Opsoclonus-Myoclonus Ataxia Syndrome: A Longitudinal Study.

Brain Volumes in Opsoclonus-Myoclonus Ataxia Syndrome: A Longitudinal Study.

Journal: Journal of child neurology

Published: March 28, 2024

Progressive Neurological Decline Associated With Intracranial Calcification in Down Syndrome; Fahr Disease Mimic?

Progressive Neurological Decline Associated With Intracranial Calcification in Down Syndrome; Fahr Disease Mimic?

Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques

Published: November 07, 2023

Methylmalonic aciduria as a biochemical marker for mitochondrial DNA depletion syndrome in patients with developmental delay and movement disorders: a case series.

Methylmalonic aciduria as a biochemical marker for mitochondrial DNA depletion syndrome in patients with developmental delay and movement disorders: a case series.

Journal: Frontiers in neurology

Published: July 21, 2023

A milder form of molybdenum cofactor deficiency type A presenting as Leigh's syndrome-like phenotype highlighting the secondary mitochondrial dysfunction: a case report.

A milder form of molybdenum cofactor deficiency type A presenting as Leigh's syndrome-like phenotype highlighting the secondary mitochondrial dysfunction: a case report.

Journal: Frontiers in neurology

Published: April 29, 2023

Long-term follow-up of an attenuated presentation of NAXE-related disease, a potentially actionable neurometabolic disease: a case report.

Long-term follow-up of an attenuated presentation of NAXE-related disease, a potentially actionable neurometabolic disease: a case report.

Journal: Frontiers in neurology

Published: April 12, 2023

Constitutional Mismatch Repair Deficiency Syndromes, a Neurofibromatosis 1 Mimicker That Hinders Timely Management.

Constitutional Mismatch Repair Deficiency Syndromes, a Neurofibromatosis 1 Mimicker That Hinders Timely Management.

Journal: Journal of pediatric hematology/oncology

Published: October 18, 2022

SLC gene mutations and pediatric neurological disorders: diverse clinical phenotypes in a Saudi Arabian population.

SLC gene mutations and pediatric neurological disorders: diverse clinical phenotypes in a Saudi Arabian population.

Journal: Human genetics

Published: July 25, 2021

Palato-Lingual Tremor in a Child With Juvenile-Onset Alexander Disease.

Palato-Lingual Tremor in a Child With Juvenile-Onset Alexander Disease.

Journal: Pediatric neurology

Published: June 02, 2021

Successful treatment of epilepsia partialis continua with perampanel: two pediatric cases.

Successful treatment of epilepsia partialis continua with perampanel: two pediatric cases.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: April 14, 2021

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Last Updated: 09/26/2026