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Journal of Child Neurology|August 21, 2018
Multiple Sulfatase Deficiency: A Case Series With a Novel MutationLeen Hijazi, Amna Kashgari, Majid Alfadhel
Journal of Pediatric Hematology/Oncology|August 21, 2020
WNT-activated Pediatric Medulloblastoma Associated With Metastasis to the Suprasellar Region and HypopituitarismNaveed Ahmad, Mohamed Eltawel, Amna Kashgari, et al.
International Journal of Pediatrics & Adolescent Medicine|August 17, 2021
A rare cerebellar vermis high-grade neuroepithelial tumor: Radiological-pathological correlationAmna Kashgari, Rases Al Otaibi, Fahd Al Sufiani, et al.
Journal of Medical Case Reports|September 2, 2025
Near-fatal asthma in a 12-year-old girl leading to life-threatening tonsillar herniation: a case reportAbdullah Almutairi, Khalid Althobaiti, Mohannad Antar, et al.
The Neuroradiology Journal|April 23, 2014
Extraneural metastasis of an ependymoma: a rare occurrenceAhmed Alzahrani, Ali Alassiri, Amna Kashgari, et al.
Frontiers in Genetics|January 31, 2024
Case report: A founder UGDH variant associated with developmental epileptic encephalopathy in Saudi ArabiaManal Alaamery, Salam Massadeh, Manar Aldarwish, et al.
ACG Case Reports Journal|February 19, 2019
Severe Crohn's Disease Manifestations in a Child with Cystathionine β-Synthase DeficiencySaud Alsahli, Aziz Al Anazi, Maher M Al Hatlani, et al.
Neurosciences (Riyadh, Saudi Arabia)|May 13, 2024
Review of the spectrum of tuberous sclerosis complex: The Saudi Arabian ExperienceMohammed Almuqbil, Waad Aldoohan, Sara Alhinti, et al.
Journal of Multidisciplinary Healthcare|March 27, 2024
Epidemiology and Outcomes of Neurofibromatosis Type 1 (NF-1): Multicenter Tertiary ExperienceMohammed Almuqbil, Fatimah Yaseen Alshaikh, Waleed Altwaijri, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 2025
Biallelic ELOVL1 Variants Are Linked to Hypomyelinating Leukodystrophy, Movement Disorder, and IchthyosisKeit Men Wong, Reza Maroofian, Kolja Meier, et al.
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