Muhammad T. Alrifai

Riyadh, Saudi Arabia

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 33 publications

Variable Phenotype in Three Siblings With RAN Binding Protein 2 Variant With Potential Preventive Treatment for Recurrences.

Variable Phenotype in Three Siblings With RAN Binding Protein 2 Variant With Potential Preventive Treatment for Recurrences.

Journal: Pediatric neurology
Published: January 16, 2026

Patterns of Response to Treatment and Outcome of Childhood Absence Epilepsy: A Multicenter Study From Saudi Arabia.

Patterns of Response to Treatment and Outcome of Childhood Absence Epilepsy: A Multicenter Study From Saudi Arabia.

Journal: Pediatric neurology
Published: December 24, 2025

Clinical Spectrum of Acquired Demyelinating Syndromes in Children: A Tertiary Hospital Experience.

Clinical Spectrum of Acquired Demyelinating Syndromes in Children: A Tertiary Hospital Experience.

Journal: Neurology and therapy
Published: February 11, 2025

Genetic Microcephaly in a Saudi Population: Unique Spectrum of Affected Genes Including a Novel One.

Genetic Microcephaly in a Saudi Population: Unique Spectrum of Affected Genes Including a Novel One.

Journal: Journal of child neurology
Published: June 07, 2024

The Response of Synthetic Adrenocorticotropic Hormone (ACTH) Treatment in Pediatric Drug-Resistant Epilepsy Other Than Infantile Epileptic Spasms Syndrome: A Retrospective Observational Study.

The Response of Synthetic Adrenocorticotropic Hormone (ACTH) Treatment in Pediatric Drug-Resistant Epilepsy Other Than Infantile Epileptic Spasms Syndrome: A Retrospective Observational Study.

Journal: Cureus
Published: September 28, 2023

Effectiveness of intra-thecal methotrexate in refractory Anti-N-methyl-d-aspartate receptor encephalitis.

Effectiveness of intra-thecal methotrexate in refractory Anti-N-methyl-d-aspartate receptor encephalitis.

Journal: BMC neurology
Published: May 17, 2023

Phenotype and genotype of 15 Saudi patients with achromatopsia: A case series.

Phenotype and genotype of 15 Saudi patients with achromatopsia: A case series.

Journal: Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society
Published: May 15, 2023

Phenotype and Genotype of Saudi Pediatric Patients With Neurofibromatosis Type 1: A Seven-Year Multicenter Experience From Saudi Arabia.

Phenotype and Genotype of Saudi Pediatric Patients With Neurofibromatosis Type 1: A Seven-Year Multicenter Experience From Saudi Arabia.

Journal: Cureus
Published: April 10, 2023

Clinical Characteristics and Risk Factors of Neonatal Hypoxic-Ischaemic Encephalopathy and Its Associated Neurodevelopmental Outcomes During the First Two Years of Life: A Retrospective Study in Saudi Arabia.

Clinical Characteristics and Risk Factors of Neonatal Hypoxic-Ischaemic Encephalopathy and Its Associated Neurodevelopmental Outcomes During the First Two Years of Life: A Retrospective Study in Saudi Arabia.

Journal: International journal of general medicine
Published: December 16, 2022

Congenital disorder of glycosylation with defective fucosylation 2 (FCSK gene defect): The third report in the literature with a mild phenotype.

Congenital disorder of glycosylation with defective fucosylation 2 (FCSK gene defect): The third report in the literature with a mild phenotype.

Journal: Molecular genetics & genomic medicine
Published: September 25, 2022

What Is the Effect of Topiramate Use on Growth in Children With Epilepsy?

What Is the Effect of Topiramate Use on Growth in Children With Epilepsy?

Journal: Cureus
Published: August 27, 2022

The response patterns of infantile spasms to treatments in 156 patients: Hormonal therapy with intravenous synthetic ACTH appears promising.

The response patterns of infantile spasms to treatments in 156 patients: Hormonal therapy with intravenous synthetic ACTH appears promising.

Journal: Neurosciences (Riyadh, Saudi Arabia)
Published: September 06, 2021
Showing 1-12 of 33

Last Updated: 09/26/2026