Publications by authors named "Muhammad T Alrifai"

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Clinical Spectrum of Acquired Demyelinating Syndromes in Children: A Tertiary Hospital Experience.
Mohammed Almuqbil, Lama Aljomah, Nora Almahmoud, Waleed Altuwaijri, Ahmad Alrumayyan, Muhammad T Alrifai

Neurol Ther· August 2025

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Genetic Microcephaly in a Saudi Population: Unique Spectrum of Affected Genes Including a Novel One.
Muhammad Talal Alrifai, Yousof Alrumayyan, Duaa Baarmah, Ahmed Alrumayyan, Waleed Altuwaijri

J Child Neurol· May 2024

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The Response of Synthetic Adrenocorticotropic Hormone (ACTH) Treatment in Pediatric Drug-Resistant Epilepsy Other Than Infantile Epileptic Spasms Syndrome: A Retrospective Observational Study.
Hajar Alammar, Ahmed Al-Rumayyan, Duaa Baarmah, Muhammad T Alrifai

Cureus· October 2023

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Phenotype and genotype of 15 Saudi patients with achromatopsia: A case series.
Enam Danish, Amal Alhashem, Reham Aljehani, Anan Aljawi, Manar M Aldarwish, Muhammad T Alrifai

Saudi J Ophthalmol· September 2023

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Effectiveness of intra-thecal methotrexate in refractory Anti-N-methyl-d-aspartate receptor encephalitis.
Raid Hommady, Abdullah Alsohibani, Ruba Alayed, Abdulaziz Alshehri, Ahlam AbuMelha, Muhammad Talal Alrifai

BMC Neurol· July 2023

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Congenital disorder of glycosylation with defective fucosylation 2 (FCSK gene defect): The third report in the literature with a mild phenotype.
Abeer Al Tuwaijri, Yusra Alyafee, Muhammad Umair, Arwa Alsubait, Mashael Alharbi, Muhammad Talal Alrifai

Mol Genet Genomic Med· April 2023

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Phenotype and Genotype of Saudi Pediatric Patients With Neurofibromatosis Type 1: A Seven-Year Multicenter Experience From Saudi Arabia.
Mohammed A Alfurayh, Nawaf K Alawad, Abdulaziz M Bin Akrish, Awad S Alharbi, Ahmed Sharahili, Muhammad T Alrifai

Cureus· April 2023

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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.
Mohammed AlMuqbil, Jawaher Alanazi, Nada Alsaif, Duaa Baarmah, Waleed Altwaijri, Muhammad Talal Alrifai

Int J Gen Med· February 2023

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What Is the Effect of Topiramate Use on Growth in Children With Epilepsy?
Muhammad T Alrifai, Noura A Alsubaie, Albatool M Abodarahem, Shadan B Alomran, Maryam N Alboqami

Cureus· August 2022

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The response patterns of infantile spasms to treatments in 156 patients: Hormonal therapy with intravenous synthetic ACTH appears promising.
Muhammad T Alrifai, Ahmad R Al-Rumayyan, Waleed A Al-Tuwaijri, Duaa M Baarmah, Safiyyah A Asiri

Neurosciences (Riyadh)· January 2022

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Pediatrics COVID-19 and neurological manifestations: Single tertiary centre experience.
Lama Aljomah, Sara Almedlej, Duaa Baarmah, Waleed Altwaijri, Ahmad Alrumayyan, Muhammad Talal Alrifai

eNeurologicalSci· September 2021

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The Leukodystrophy Spectrum in Saudi Arabia: Epidemiological, Clinical, Radiological, and Genetic Data.
Majid Alfadhel, Mohammed Almuqbil, Fuad Al Mutairi, Muhammad Umair, Mohammed Almannai, Muhammad Talal Alrifai

Front Pediatr· May 2021

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Biallelic loss-of-function variants in NEMF cause central nervous system impairment and axonal polyneuropathy.
Ashfaque Ahmed, Meng Wang, Gaber Bergant, Reza Maroofian, Rongjuan Zhao, Muhammad Talal AlRifai

Hum Genet· April 2021

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EMC10 homozygous variant identified in a family with global developmental delay, mild intellectual disability, and speech delay.
Muhammad Umair, Mariam Ballow, Abdulaziz Asiri, Yusra Alyafee, Abeer Al Tuwaijri, Muhammad Talal Alrifai

Clin Genet· December 2020

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Genomic testing and counseling: The contribution of next-generation sequencing to epilepsy genetics.
Lamia Alsubaie, Taghrid Aloraini, Manal Amoudi, Abdulrahman Swaid, Wafaa Eyiad, Muhammad Talal Alrifai

Ann Hum Genet· November 2020

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Acute Necrotizing Encephalopathy of Childhood: A Multicenter Experience in Saudi Arabia.
Fahad A Bashiri, Sultan Al Johani, Muddathir H Hamad, Amal Y Kentab, Ali H Alwadei, Muhammad Talal Alrifai

Front Pediatr· October 2020

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Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screening.
Majid Alfadhel, Muhammad Umair, Bader Almuzzaini, Saif Alsaif, Sulaiman A AlMohaimeed, Muhammad T Alrifai

Ann Clin Transl Neurol· October 2019

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The comorbidity of headaches in pediatric epilepsy patients: How common and what types?
Hanin Al-Gethami, Muhammad T Alrifai, Ahmed AlRumayyan, Waleed AlTuwaijri, Duaa Baarmah

Neurosciences (Riyadh)· October 2019

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Clinical Presentation and outcome of acute disseminated encephalomyelitis in Saudi Arabia. Tertiary Center Experience.
Bander A Aldamkh, Abdalaziz F Alamer, Mohammed M Altuwaijri, Mohammed A Alrumayyan, Abdulaziz H Alhaqbani, Muhammad T Alrifai

Neurosciences (Riyadh)· April 2019

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Prevalence and outcomes of Guillain-Barré syndrome among pediatrics in Saudi Arabia: a 10-year retrospective study.
Safiyyah Asiri, Waleed A Altwaijri, Duaa Ba-Armah, Ahmed Al Rumayyan, Muhammad T Alrifai

Neuropsychiatr Dis Treat· March 2019

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Epilepsy in Propionic Acidemia: Case Series of 14 Saudi Patients.
Afnan AlGhamdi, Muhammad Talal Alrifai, Abdullah I Al Hammad, Fuad Al Mutairi, Abdulrahman Alswaid

J Child Neurol· October 2018

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Retrospective review of pediatric status epilepticus in 116 Saudi patients: predictors of outcome.
Raid Harb Hommady, Muhammad Talal Alrifai, Osama Khaled Mubayrik, Ruba Salem Alayed, Muhannad Abdulrahman Alsemari

Ann Saudi Med· July 2018

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Extending the ophthalmological phenotype of Galloway-Mowat syndrome with distinct retinal dysfunction: a report and review of ocular findings.
Maha A Al-Rakan, Manal D Abothnain, Muhammad T Alrifai, Majid Alfadhel

BMC Ophthalmol· June 2018

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Further Delineation of the Clinical Phenotype of Cerebellar Ataxia, Mental Retardation, and Disequilibrium Syndrome Type 4.
Saud Alsahli, Muhammad Talal Alrifai, Saeed Al Tala, Fuad Al Mutairi, Majid Alfadhel

J Cent Nerv Syst Dis· February 2018

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Further delineation of the phenotypic spectrum of ISCA2 defect: A report of ten new cases.
Majid Alfadhel, Marwan Nashabat, Muhammad Talal Alrifai, Hesham Alshaalan, Fuad Al Mutairi

Eur J Paediatr Neurol· January 2018

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