Khalid J. Hundallah

Riyadh, Saudi Arabia

Last Updated: 09/26/2026

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Found 44 publications

Evaluating the pediatric neurology training curriculum in SCFHS-accredited programs: a multi-institutional survey study.

Evaluating the pediatric neurology training curriculum in SCFHS-accredited programs: a multi-institutional survey study.

Journal: BMC medical education

Published: February 24, 2026

Clinical and Genetic Spectrum of SCN8A-Related Disorders: A Retrospective Study From the Gulf Region.

Clinical and Genetic Spectrum of SCN8A-Related Disorders: A Retrospective Study From the Gulf Region.

Journal: Journal of child neurology

Published: December 01, 2025

Unlocking MENA's potential in rare-disease precision medicine.

Unlocking MENA's potential in rare-disease precision medicine.

Journal: Orphanet journal of rare diseases

Published: November 12, 2025

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.

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

Exploring the clinical, neuroimaging, and genetic spectrum of PLPBP deficiency: multicenter case series and systematic review.

Exploring the clinical, neuroimaging, and genetic spectrum of PLPBP deficiency: multicenter case series and systematic review.

Journal: Molecular genetics and metabolism

Published: September 22, 2025

Case Report: Hypomyelinating Leukodystrophy Type 20 (HLD20) With Novel CNP Gene Variant.

Case Report: Hypomyelinating Leukodystrophy Type 20 (HLD20) With Novel CNP Gene Variant.

Journal: American journal of medical genetics. Part A

Published: January 26, 2025

CIC variants and folinic acid-responsive seizures.

CIC variants and folinic acid-responsive seizures.

Journal: Molecular genetics and metabolism

Published: August 19, 2024

Multiplex Consanguineous Family Highlights CLASP1 as a Candidate Gene for Lissencephaly.

Multiplex Consanguineous Family Highlights CLASP1 as a Candidate Gene for Lissencephaly.

Journal: Neurology. Genetics

Published: May 13, 2024

Loss-of-function variants in JPH1 cause congenital myopathy with prominent facial and ocular involvement.

Loss-of-function variants in JPH1 cause congenital myopathy with prominent facial and ocular involvement.

Journal: Journal of medical genetics

Published: March 03, 2024

Editorial Message.

Editorial Message.

Journal: Neurosciences (Riyadh, Saudi Arabia)

Published: January 09, 2024

Diagnosis and management of infantile epileptic spasms syndrome (IESS) in Gulf Cooperation Council (GCC) countries: Expert consensus statement.

Diagnosis and management of infantile epileptic spasms syndrome (IESS) in Gulf Cooperation Council (GCC) countries: Expert consensus statement.

Journal: Seizure

Published: December 06, 2023

Novel TLR7 hemizygous variant in post-COVID-19 neurological deterioration: a case report with literature review.

Novel TLR7 hemizygous variant in post-COVID-19 neurological deterioration: a case report with literature review.

Journal: Frontiers in neurology

Published: July 30, 2023

Showing 1-12 of 44

Last Updated: 09/26/2026