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Neurology and Therapy|January 4, 2025
Administration and Monitoring Burden of High-Efficacy Disease-Modifying Therapies for Multiple Sclerosis: A Delphi Consensus of Clinical Experts from Saudi ArabiaSeraj Makkawi, Ahmad Abulaban, Yaser Al Malik, et al.
BMC Medical Genetics|July 6, 2019
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegiaSalma M Wakil, Safa Alhissi, Haya Al Dossari, et al.
World Neurosurgery|October 1, 2019
Predictors of Surgical Site Infection in Autologous Cranioplasty: A Retrospective Analysis of Subcutaneously Preserved Bone Flaps in Abdominal PocketsAli Alkhaibary, Ahoud Alharbi, Munzir Abbas, et al.
Case Reports in Surgery|June 17, 2024
Giant Ganglioneuroma of the Lumbar Spine: A Rare Cause of RadiculopathyLina Altalhi, Abdulaziz Alayyaf, Mohammed Bin-Mahfooz, et al.
The International Journal of Neuroscience|February 19, 2011
Will new injection devices for interferon β-1a s.c. affect treatment adherence in patients with multiple sclerosis? An expert opinion in the Middle EastDirk Deleu, Issa Alsharoqi, Mohammed Ali Al Jumah, et al.
Stereotactic and Functional Neurosurgery|April 30, 2026
Psychiatric Neurosurgery: Attitude and Barriers of Psychiatrists Toward Neurosurgical Interventions in Saudi ArabiaLaila Alqahtani, Reem Abdulaziz Albuhairan, Mohammed Abdulmohsen Alsaif, et al.
Parkinsonism & Related Disorders|February 22, 2023
Expanding the genotype-phenotype landscape of PDE10A-associated movement disordersSaeed Bohlega, Ali H Abusrair, Zainah Al-Qahtani, et al.
Gene|December 10, 2013
Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>TSalma M Wakil, Khushnooda Ramzan, Rula Abuthuraya, et al.
Case Reports in Surgery|January 25, 2022
Hypothalamic Lipoma: Outcome of an Intracranial Developmental LesionAli Alkhaibary, Noura Alsubaie, Ahoud Alharbi, et al.
Human Mutation|November 9, 2011
A missense mutation in PIK3R5 gene in a family with ataxia and oculomotor apraxiaNada Al Tassan, Dania Khalil, Jameela Shinwari, et al.
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