Treating epilepsy with options other than antiepileptic medications

por Muthaffar, Osama Y.
Publicado 2020

Brain Magnetic Resonance Imaging Findings in Infantile Spasms

por Muthaffar, Osama Y.
Publicado 2022

A novel homozygous splice donor variant in the LRPPRC gene causing Leigh syndrome with epilepsy, a French-Canadian disorder in a Saudi family: case report

por Muthaffar, Osama Y., Abdulkareem, Angham Abdulrhman, Ashi, Abrar, Naseer, Muhammad Imran
Publicado 2023

Whole-Exome Sequencing Reveals a Missense Variant c.1612C>T (p.Arg538Cys) in the BTD Gene Leading to Neuromyelitis Optica Spectrum Disorder in Saudi Families

por Naseer, Muhammad Imran, Pushparaj, Peter Natesan, Abdulkareem, Angham Abdulrahman, Muthaffar, Osama Y.
Publicado 2022

Insight into Genetic Mutations of SZT2: Is It a Syndrome?

por Muthaffar, Osama Y., Jan, Mohammed M. S., Alyazidi, Anas S., Alotibi, Taif K., Alsulami, Eman A.
Publicado 2023

Next-Generation Sequencing Reveals Novel Homozygous Missense Variant c.934T > C in POLR1C Gene Causing Leukodystrophy and Hypomyelinating Disease

por Naseer, Muhammad Imran, Abdulkareem, Angham Abdulrahman, Pushparaj, Peter Natesan, Saharti, Samah, Muthaffar, Osama Y.
Publicado 2022

Valproic acid for children below 2 years of age with epilepsy

por Muthaffar, Osama Y., Almahmudi, Salha M., Alrabghi, Muna O., Bin Mahfouz, Maria M., Alfawaz, Nuha S.
Publicado 2021

Clinical whole exome sequencing revealed de novo heterozygous stop-gain and missense variants in the STXBP1 gene associated with epilepsy in Saudi families

por Naseer, Muhammad Imran, Abdulkareem, Angham Abdulrhman, Rasool, Mahmood, Shirah, Bader, Algahtani, Hussein, Muthaffar, Osama Y., Pushparaj, Peter Natesan
Publicado 2022

Evaluation of Health Science Students’ Health Fatalism and Perception Towards Patients With Epilepsy: A Cross-Sectional Global Study

por Alyazidi, Anas S, Muthaffar, Osama Y, Alotibi, Fahad A, Almubarak, Albatool, Tamai, Luca, Takieddin, Siba Z, Alghamdi, Maha, Alraddadi, Yara K
Publicado 2022

Treatment of infantile spasms in Saudi Arabia

por Alqassas, Maryam A., Muthaffar, Osama Y., Aljawi, Anan A., Taj, Ahad M., Nijaifan, Haya K., Alyoubi, Reem A., Jan, Mohammed M.
Publicado 2018

GAMT Deficiency Among Pediatric Population: Clinical and Molecular Characteristics and Management

por Almaghrabi, Majdah A., Muthaffar, Osama Y., Alahmadi, Sereen A., Abdulsbhan, Mashael A., Bamusa, Mashael, Aljezani, Maram Ahmed, Bahowarth, Sarah Y., Alyazidi, Anas S., Aggad, Waheeb S.
Publicado 2023

Consensus Statement on the Management of Duchenne Muscular Dystrophy in Saudi Arabia During the Coronavirus Disease 2019 Pandemic

por Bamaga, Ahmed K., Alghamdi, Fouad, Alshaikh, Nahla, Altwaijri, Waleed, Bashiri, Fahad A., Hundallah, Khalid, Abukhaled, Musaad, Muthaffar, Osama Y., Al-Mehmadi, Sameer, Jamaly, Tahani Ahmed, Al-Muhaizea, Mohammad A., Al-Saman, Abdulaziz
Publicado 2021