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Sultan Qaboos University Medical Journal|September 1, 2023
Guillain-Barré Syndrome Associated with SARS-CoV-2 in Two Pediatric PatientsFatema Al Amrani, Raghad Al-Abdwani, Fatma Al Rashdi, et al.
Pediatric Neurology|October 4, 2017
Intravenous Immunoglobulin as a Treatment for Intractable Epilepsy Secondary to Focal Cortical Dysplasia: A Meta-analysisFatema Al Amrani, Roy Dudley, Luis E Bello-Espinosa, et al.
American Journal of Medical Genetics. Part A|October 3, 2024
Periodic Paralysis in a Child With Thermosensitive Mitochondrial Trifunctional Protein DeficiencyFatema Al-Amrani, Jos P N Ruiter, Mirjam Doolaard, et al.
Cureus|December 1, 2025
Parry-Romberg Syndrome With Localized Scleroderma: A Report of Two Pediatric Cases From OmanManhal H Al Lawati, Wafaa Al Shehhi, Fatema Al Amrani, et al.
Pediatric Neurology|September 9, 2023
Autosomal Recessive NOTCH3-Related Leukodystrophy in Two Siblings and Review of the LiteratureFatema Al-Amrani, Almundher Al-Maawali, Khalid Al-Thihli, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 15, 2018
Prediction of outcome in asphyxiated newborns treated with hypothermia: Is a MRI scoring system described before the cooling era still useful?Fatema Al Amrani, Jaclyn Marcovitz, Priscille-Nice Sanon, et al.
Sultan Qaboos University Medical Journal|September 5, 2024
Aetiology and Outcome of Childhood Convulsive Status Epilepticus: A tertiary care experience in OmanAreeba Wasim, Shihab S Al Maawali, Abdulrahman S AlJabri, et al.
Pediatric Pulmonology|October 4, 2022
Respiratory characteristics in children with spinal muscular atrophy type 1 receiving nusinersenLena Xiao, Jackie Chiang, Maria Castro-Codesal, et al.
The Pediatric Infectious Disease Journal|November 11, 2025
Influenza-associated Neurologic Complications in Children: Insights From a Single-center Study in OmanJuhaina Al-Rashdi, Fatma BaAlawi, Khuloud Al Maamari, et al.
Medrxiv : the Preprint Server for Health Sciences|March 22, 2023
Variants in ACTC1 underlie distal arthrogryposis accompanied by congenital heart defectsJessica X Chong, Matthew Carter Childers, Colby T Marvin, et al.
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