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Neurosciences (Riyadh, Saudi Arabia)|March 8, 2019
Effect of new modalities of treatment on physicians management plan for patients with spinal muscular atrophyFahad A Bashiri, Hiyam A Idris, Fahad M Al-Sohime, et al.
Sudanese Journal of Paediatrics|August 6, 2016
Sturge-Weber syndrome: Continued vigilance is neededSaeed Hassan, Amir Babiker, Fahad A Bashiri, et al.
European Journal of Medical Genetics|January 19, 2020
Expanding the phenotype and the genotype of Stromme syndrome: A novel variant of the CENPF gene and literature reviewMalak Alghamdi, Waleed H Alkhamis, Fahad A Bashiri, et al.
Sudanese Journal of Paediatrics|February 26, 2019
Drowning in the desert: family denial of brain deathMohamad-Hani Temsah, Fahad Alsohaim, Ayman Al-Eyadhy, et al.
Children (Basel, Switzerland)|August 26, 2023
Genotype-Phenotype Analysis of Children with Epilepsy Referred for Whole-Exome Sequencing at a Tertiary Care University HospitalFahad A Bashiri, Rawan AlSheikh, Muddathir H Hamad, et al.
Neurosciences (Riyadh, Saudi Arabia)|February 19, 2018
Respiratory support attitudes among pediatric intensive care staff for spinal muscular atrophy patients in Saudi ArabiaMohamad-Hani A Temsah, Fahad M Al-Sohime, Fahad A Bashiri, et al.
Neurosciences (Riyadh, Saudi Arabia)|February 2, 2021
Neurodevelopmental and epilepsy outcomes of patients with infantile spasms treated in a tertiary care centerFahad A Bashiri, Matar A Al-Sehemi, Muddathir H Hamad, et al.
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