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Frontiers in Pediatrics|March 8, 2021
Consensus Statement on the Management of Duchenne Muscular Dystrophy in Saudi Arabia During the Coronavirus Disease 2019 PandemicAhmed K Bamaga, Fouad Alghamdi, Nahla Alshaikh, et al.
Frontiers in Oncology|November 6, 2024
Corrigendum: Diagnosis and management of neurofibromatosis type 1 in Arabian Gulf Cooperation Council Region: challenges and recommendationsFahad A Bashiri, Khaled Hundallah, Musaad Abukhaled, et al.
Frontiers in Oncology|September 11, 2024
Diagnosis and management of neurofibromatosis type 1 in Arabian Gulf Cooperation Council Region: challenges and recommendationsFahad A Bashiri, Khaled Hundallah, Musaad Abukhaled, et al.
Frontiers in Public Health|October 14, 2022
Mental health impact of COVID-19 on Saudi families and children with special educational needs and disabilities in Saudi Arabia: A national perspectiveShuliweeh Alenezi, Mohamad-Hani Temsah, Ahmed S Alyahya, et al.
Healthcare (Basel, Switzerland)|April 14, 2026
Genetic, Clinical, and Management Characteristics of Duchenne Muscular Dystrophy in Saudi ArabiaAbdulaziz S AlSaman, Fouad Al Ghamdi, Ahmed K Bamaga, et al.
International Journal of Pediatrics & Adolescent Medicine|June 4, 2021
Effect of lumbar puncture educational video on parental knowledge and self-reported intended practiceMohamad-Hani Temsah, Ayman Al-Eyadhy, Fahad Alsohime, et al.
Cureus|July 4, 2024
Virtual Objective Structured Clinical Examination (OSCE) Training in the Pandemic Era: Feasibility, Satisfaction, and the Road AheadElshazaly Saeed, Muddathir H Hamad, Abdullah N Alhuzaimi, et al.
Frontiers in Public Health|September 18, 2025
Emotional coping strategies in children with and without special educational needs during the COVID-19 pandemic in Saudi ArabiaShuliweeh Alenezi, Mohammed Alarabi, Ahmed S Alyahya, et al.
Seizure|March 3, 2024
Diagnosis and management of infantile epileptic spasms syndrome (IESS) in Gulf Cooperation Council (GCC) countries: Expert consensus statementFahad A Bashiri, Khalid Hundallah, Raidah Al-Baradie, et al.
American Journal of Human Genetics|June 3, 2017
Mutations in NKX6-2 Cause Progressive Spastic Ataxia and HypomyelinationViorica Chelban, Nisha Patel, Jana Vandrovcova, et al.
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