Search Results - Osama Y Muthaffar

Brain Magnetic Resonance Imaging Findings in Infantile Spasms by Osama Y. Muthaffar

Connect to this object online.

Parental perceptions of dental health in children with neurological disorders: Cross-sectional tertiary care center assessment by Anas S Alyazidi, Sara Y Muthaffar, Arwa Y Muthaffar, Osama Y Muthaffar, Mahmoud A Gaddoury

Connect to this object online.

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 by Osama Y. Muthaffar, Angham Abdulrhman Abdulkareem, Angham Abdulrhman Abdulkareem, Abrar Ashi, Abrar Ashi, Muhammad Imran Naseer, Muhammad Imran Naseer

Connect to this object online.

Consensus Statement on the Management of Duchenne Muscular Dystrophy in Saudi Arabia During the Coronavirus Disease 2019 Pandemic by Ahmed K. Bamaga, Ahmed K. Bamaga, Fouad Alghamdi, Nahla Alshaikh, Nahla Alshaikh, Nahla Alshaikh, Waleed Altwaijri, Waleed Altwaijri, Fahad A. Bashiri, Fahad A. Bashiri, Khalid Hundallah, Musaad Abukhaled, Osama Y. Muthaffar, Osama Y. Muthaffar, Sameer Al-Mehmadi, Tahani Ahmed Jamaly, Mohammad A. Al-Muhaizea, Abdulaziz Al-Saman

Connect to this object online.

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 by Muhammad Imran Naseer, Muhammad Imran Naseer, Peter Natesan Pushparaj, Peter Natesan Pushparaj, Peter Natesan Pushparaj, Angham Abdulrahman Abdulkareem, Angham Abdulrahman Abdulkareem, Osama Y. Muthaffar

Connect to this object online.

Next-Generation Sequencing Reveals Novel Homozygous Missense Variant c.934T > C in POLR1C Gene Causing Leukodystrophy and Hypomyelinating Disease by Muhammad Imran Naseer, Muhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Angham Abdulrahman Abdulkareem, Peter Natesan Pushparaj, Peter Natesan Pushparaj, Peter Natesan Pushparaj, Samah Saharti, Osama Y. Muthaffar

Connect to this object online.