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Osama Y Muthaffar

Showing results (1-10 of 31) with videos related to

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Neurology International|March 24, 2022
Brain Magnetic Resonance Imaging Findings in Infantile SpasmsOsama Y Muthaffar
Neurosciences (Riyadh, Saudi Arabia)|November 1, 2020
Treating epilepsy with options other than antiepileptic medicationsOsama Y Muthaffar
Neurosciences (Riyadh, Saudi Arabia)|April 18, 2014
Public awareness and attitudes toward epilepsy in Saudi Arabia is improvingOsama Y Muthaffar, Mohammed M Jan
Neurosciences (Riyadh, Saudi Arabia)|May 13, 2024
Epilepsia partialis continua: A reviewOsama Y Muthaffar, Anas S Alyazidi
Cureus|August 5, 2024
Prevalence of Seizures in Children Diagnosed With Neurodevelopmental DisordersOsama Y Muthaffar, Abrar Y Abbar, Mohammed T Fitaih
Saudi Medical Journal|August 18, 2014
Acute hemiplegia as a rare presentation of infantile Guillain-Barré syndromeOsama Y Muthaffar, Adel A Mahmoud, Abdulaziz S Al-Saman
Frontiers in Pediatrics|December 4, 2023
A novel homozygous splice donor variant in the <i>LRPPRC</i> gene causing Leigh syndrome with epilepsy, a French-Canadian disorder in a Saudi family: case reportOsama Y Muthaffar, Angham Abdulrhman Abdulkareem, Abrar Ashi, et al.
Frontiers in Pediatrics|March 10, 2022
Whole-Exome Sequencing Reveals a Missense Variant c.1612C>T (p.Arg538Cys) in the <i>BTD</i> Gene Leading to Neuromyelitis Optica Spectrum Disorder in Saudi FamiliesMuhammad Imran Naseer, Peter Natesan Pushparaj, Angham Abdulrahman Abdulkareem, et al.
Cureus|March 19, 2024
Giant Axonal Neuropathy: A Case Report of Subclinical Childhood ManifestationsAhmed K Bamaga, Osama Y Muthaffar, Anas S Alyazidi, et al.
Frontiers in Pediatrics|June 10, 2022
Next-Generation Sequencing Reveals Novel Homozygous Missense Variant c.934T > C in <i>POLR1C</i> Gene Causing Leukodystrophy and Hypomyelinating DiseaseMuhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Peter Natesan Pushparaj, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Neurology International|March 24, 2022
Brain Magnetic Resonance Imaging Findings in Infantile SpasmsOsama Y Muthaffar
Neurosciences (Riyadh, Saudi Arabia)|November 1, 2020
Treating epilepsy with options other than antiepileptic medicationsOsama Y Muthaffar
Neurosciences (Riyadh, Saudi Arabia)|April 18, 2014
Public awareness and attitudes toward epilepsy in Saudi Arabia is improvingOsama Y Muthaffar, Mohammed M Jan
Neurosciences (Riyadh, Saudi Arabia)|May 13, 2024
Epilepsia partialis continua: A reviewOsama Y Muthaffar, Anas S Alyazidi
Cureus|August 5, 2024
Prevalence of Seizures in Children Diagnosed With Neurodevelopmental DisordersOsama Y Muthaffar, Abrar Y Abbar, Mohammed T Fitaih
Saudi Medical Journal|August 18, 2014
Acute hemiplegia as a rare presentation of infantile Guillain-Barré syndromeOsama Y Muthaffar, Adel A Mahmoud, Abdulaziz S Al-Saman
Frontiers in Pediatrics|December 4, 2023
A novel homozygous splice donor variant in the <i>LRPPRC</i> gene causing Leigh syndrome with epilepsy, a French-Canadian disorder in a Saudi family: case reportOsama Y Muthaffar, Angham Abdulrhman Abdulkareem, Abrar Ashi, et al.
Frontiers in Pediatrics|March 10, 2022
Whole-Exome Sequencing Reveals a Missense Variant c.1612C>T (p.Arg538Cys) in the <i>BTD</i> Gene Leading to Neuromyelitis Optica Spectrum Disorder in Saudi FamiliesMuhammad Imran Naseer, Peter Natesan Pushparaj, Angham Abdulrahman Abdulkareem, et al.
Cureus|March 19, 2024
Giant Axonal Neuropathy: A Case Report of Subclinical Childhood ManifestationsAhmed K Bamaga, Osama Y Muthaffar, Anas S Alyazidi, et al.
Frontiers in Pediatrics|June 10, 2022
Next-Generation Sequencing Reveals Novel Homozygous Missense Variant c.934T > C in <i>POLR1C</i> Gene Causing Leukodystrophy and Hypomyelinating DiseaseMuhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Peter Natesan Pushparaj, et al.
Pageof 4