Osama Yousef Muthaffar (Osama Muthaffar, Osama Y Muthaffar)

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 31

Top Topics

Magnetic Resonance

Top Venues

Neurosciences (Riyadh, Saudi Arabia)

Genes & genomics

Translational pediatrics

This page only lists publications with an associated author ORCID identifier.

Publications

Osama Yousef Muthaffar, Asma Alqarni, Jumana A Shafei, Sarah Y Bahowarth, Anas S Alyazidi, Muhammad Imran Naseer
Childhood-related neural genotype-phenotype in ATP1A3 mutations: comprehensive analysis. Genes & genomics 46 (4) (2024)
Osama Yousef Muthaffar, Asma Alqarni, Jumana A Shafei, Sarah Y Bahowarth, Anas S Alyazidi, Muhammad Imran Naseer
Childhood-related neural genotype-phenotype in ATP1A3 mutations: comprehensive analysis. Genes & genomics 46 (4) (2024)
Osama Yousef Muthaffar, Anas S Alyazidi
Epilepsia partialis continua: A review. Neurosciences (Riyadh, Saudi Arabia) 29 (2) (2024)
Osama Yousef Muthaffar, Anas S Alyazidi
Epilepsia partialis continua: A review. Neurosciences (Riyadh, Saudi Arabia) 29 (2) (2024)
Osama Yousef Muthaffar, Asma Alqarni, Jumana A Shafei, Sarah Y Bahowarth, Anas S Alyazidi, Muhammad Imran Naseer
Childhood-related neural genotype-phenotype in ATP1A3 mutations: comprehensive analysis. Genes & genomics 46 (4) (2024)
Osama Yousef Muthaffar, Asma Alqarni, Jumana A Shafei, Sarah Y Bahowarth, Anas S Alyazidi, Muhammad Imran Naseer
Childhood-related neural genotype-phenotype in ATP1A3 mutations: comprehensive analysis. Genes & genomics 46 (4) (2024)
Osama Yousef Muthaffar, Ahmed K Bamaga, Anas S Alyazidi, Layan S Baaishrah, Hussain A Alkhalifah, Rafah B Hariri, Maya S Khider, Sereen A Alahmadi
Efficacy and tolerability of perampanel in pediatric patients with Dravet syndrome. Translational pediatrics 13 (4) (2024)
Osama Yousef Muthaffar, Ahmed K Bamaga, Anas S Alyazidi, Layan S Baaishrah, Hussain A Alkhalifah, Rafah B Hariri, Maya S Khider, Sereen A Alahmadi
Efficacy and tolerability of perampanel in pediatric patients with Dravet syndrome. Translational pediatrics 13 (4) (2024)
Osama Yousef Muthaffar, Noura W Alazhary, Anas S Alyazidi, Mohammed A Alsubaie, Sarah Y Bahowarth, Nour B Odeh, Ahmed K Bamaga
Clinical description and evaluation of 30 pediatric patients with ultra-rare diseases: A multicenter study with real-world data from Saudi Arabia. PloS one 19 (7) (2024)
Osama Yousef Muthaffar, Anas S Alyazidi
Epilepsia partialis continua: A review. Neurosciences (Riyadh, Saudi Arabia) 29 (2) (2024)
Osama Yousef Muthaffar, Noura W Alazhary, Anas S Alyazidi, Mohammed A Alsubaie, Sarah Y Bahowarth, Nour B Odeh, Ahmed K Bamaga
Clinical description and evaluation of 30 pediatric patients with ultra-rare diseases: A multicenter study with real-world data from Saudi Arabia. PloS one 19 (7) (2024)
Osama Yousef Muthaffar, Anas S Alyazidi
Epilepsia partialis continua: A review. Neurosciences (Riyadh, Saudi Arabia) 29 (2) (2024)
Osama Yousef Muthaffar, Asma Alqarni, Jumana A Shafei, Sarah Y Bahowarth, Anas S Alyazidi, Muhammad Imran Naseer
Childhood-related neural genotype-phenotype in ATP1A3 mutations: comprehensive analysis. Genes & genomics (2024)
Mudhawi Alhiniah, Asma Alshahrani, Renad Rajab, Rakan Alelyani, Atheer Badawi, Abrar Abbar, Mashael Abdulsbhan, Amir Alrajhi, Osama Yousef Muthaffar, Mohammed Jan
Treatment of drop attacks: Anti-seizure drug choices of pediatric neurologists in Saudi Arabia. Neurosciences (Riyadh, Saudi Arabia) 28 (3) (2023)
Qaiser Zaman, Muhammad Abbas Khan, Kalsoom Sahar, Gauhar Rehman, Hamza Khan, Mehwish Rehman, null Najumuddin, Ilyas Ahmad, Muhmmad Tariq, Osama Yousef Muthaffar, Angham Abdulrhman Abdulkareem, Fehmida Bibi, Muhammad Imran Naseer, Muhammad Shah Faisal, Naveed Wasif, Musharraf Jelani
Novel Variants in MPV17, PRX, GJB1 , and SACS Cause Charcot-Marie-Tooth and Spastic Ataxia of Charlevoix-Saguenay Type Diseases. Genes 14 (2) (2023)
Qaiser Zaman, Muhammad Abbas Khan, Kalsoom Sahar, Gauhar Rehman, Hamza Khan, Mehwish Rehman, null Najumuddin, Ilyas Ahmad, Muhmmad Tariq, Osama Yousef Muthaffar, Angham Abdulrhman Abdulkareem, Fehmida Bibi, Muhammad Imran Naseer, Muhammad Shah Faisal, Naveed Wasif, Musharraf Jelani
Novel Variants in MPV17, PRX, GJB1 , and SACS Cause Charcot-Marie-Tooth and Spastic Ataxia of Charlevoix-Saguenay Type Diseases. Genes 14 (2) (2023)
Ahmed Elmardenly, Zekra Aljehani, Abdullah Tamim, Anas S Alyazidi, Osama Yousef Muthaffar
Efficacy and Safety of Perampanel in Children with Drug-Resistant Focal-Onset Seizures: A Retrospective Review. Children (Basel, Switzerland) 10 (6) (2023)
Ahmed Elmardenly, Zekra Aljehani, Abdullah Tamim, Anas S Alyazidi, Osama Yousef Muthaffar
Efficacy and Safety of Perampanel in Children with Drug-Resistant Focal-Onset Seizures: A Retrospective Review. Children (Basel, Switzerland) 10 (6) (2023)
Qaiser Zaman, null Sadeeda, Muhammad Anas, Gauhar Rehman, Qadeem Khan, Aiman Iftikhar, Mashal Ahmad, Muhammad Owais, Ilyas Ahmad, Osama Yousef Muthaffar, Angham Abdulrhman Abdulkareem, Fehmida Bibi, Musharraf Jelani, Muhammad Imran Naseer
Report of Hermansky-Pudlak Syndrome in Two Families with Novel Variants in HPS3 and HPS4 Genes. Genes 14 (1) (2023)
Abu Bakar, Sulaiman Shams, Nousheen Bibi, Asmat Ullah, Wasim Ahmad, Musharraf Jelani, Osama Yousef Muthaffar, Angham Abdulrhman Abdulkareem, Turki S Abujamel, Absarul Haque, Muhammad Imran Naseer, Bushra Khan
A Novel Homozygous Nonsense Variant in the DYM Underlies Dyggve-Melchior-Clausen Syndrome in Large Consanguineous Family. Genes 14 (2) (2023)
Osama Yousef Muthaffar, Mohammed M S Jan, Anas S Alyazidi, Taif K Alotibi, Eman A Alsulami
Insight into Genetic Mutations of SZT2: Is It a Syndrome? Biomedicines 11 (9) (2023)
Qaiser Zaman, Muhammad Abbas Khan, Kalsoom Sahar, Gauhar Rehman, Hamza Khan, Mehwish Rehman, null Najumuddin, Ilyas Ahmad, Muhmmad Tariq, Osama Yousef Muthaffar, Angham Abdulrhman Abdulkareem, Fehmida Bibi, Muhammad Imran Naseer, Muhammad Shah Faisal, Naveed Wasif, Musharraf Jelani
Novel Variants in MPV17, PRX, GJB1 , and SACS Cause Charcot-Marie-Tooth and Spastic Ataxia of Charlevoix-Saguenay Type Diseases. Genes 14 (2) (2023)
Abu Bakar, Sulaiman Shams, Nousheen Bibi, Asmat Ullah, Wasim Ahmad, Musharraf Jelani, Osama Yousef Muthaffar, Angham Abdulrhman Abdulkareem, Turki S Abujamel, Absarul Haque, Muhammad Imran Naseer, Bushra Khan
A Novel Homozygous Nonsense Variant in the DYM Underlies Dyggve-Melchior-Clausen Syndrome in Large Consanguineous Family. Genes 14 (2) (2023)
Abu Bakar, Sulaiman Shams, Nousheen Bibi, Asmat Ullah, Wasim Ahmad, Musharraf Jelani, Osama Yousef Muthaffar, Angham Abdulrhman Abdulkareem, Turki S Abujamel, Absarul Haque, Muhammad Imran Naseer, Bushra Khan
A Novel Homozygous Nonsense Variant in the DYM Underlies Dyggve-Melchior-Clausen Syndrome in Large Consanguineous Family. Genes 14 (2) (2023)
Qaiser Zaman, null Sadeeda, Muhammad Anas, Gauhar Rehman, Qadeem Khan, Aiman Iftikhar, Mashal Ahmad, Muhammad Owais, Ilyas Ahmad, Osama Yousef Muthaffar, Angham Abdulrhman Abdulkareem, Fehmida Bibi, Musharraf Jelani, Muhammad Imran Naseer
Report of Hermansky-Pudlak Syndrome in Two Families with Novel Variants in HPS3 and HPS4 Genes. Genes 14 (1) (2023)
Qaiser Zaman, null Sadeeda, Muhammad Anas, Gauhar Rehman, Qadeem Khan, Aiman Iftikhar, Mashal Ahmad, Muhammad Owais, Ilyas Ahmad, Osama Yousef Muthaffar, Angham Abdulrhman Abdulkareem, Fehmida Bibi, Musharraf Jelani, Muhammad Imran Naseer
Report of Hermansky-Pudlak Syndrome in Two Families with Novel Variants in HPS3 and HPS4 Genes. Genes 14 (1) (2023)
Qaiser Zaman, null Sadeeda, Muhammad Anas, Gauhar Rehman, Qadeem Khan, Aiman Iftikhar, Mashal Ahmad, Muhammad Owais, Ilyas Ahmad, Osama Yousef Muthaffar, Angham Abdulrhman Abdulkareem, Fehmida Bibi, Musharraf Jelani, Muhammad Imran Naseer
Report of Hermansky-Pudlak Syndrome in Two Families with Novel Variants in HPS3 and HPS4 Genes. Genes 14 (1) (2023)
Qaiser Zaman, Muhammad Abbas Khan, Kalsoom Sahar, Gauhar Rehman, Hamza Khan, Mehwish Rehman, null Najumuddin, Ilyas Ahmad, Muhmmad Tariq, Osama Yousef Muthaffar, Angham Abdulrhman Abdulkareem, Fehmida Bibi, Muhammad Imran Naseer, Muhammad Shah Faisal, Naveed Wasif, Musharraf Jelani
Novel Variants in MPV17, PRX, GJB1 , and SACS Cause Charcot-Marie-Tooth and Spastic Ataxia of Charlevoix-Saguenay Type Diseases. Genes 14 (2) (2023)
Qaiser Zaman, null Sadeeda, Muhammad Anas, Gauhar Rehman, Qadeem Khan, Aiman Iftikhar, Mashal Ahmad, Muhammad Owais, Ilyas Ahmad, Osama Yousef Muthaffar, Angham Abdulrhman Abdulkareem, Fehmida Bibi, Musharraf Jelani, Muhammad Imran Naseer
Report of Hermansky-Pudlak Syndrome in Two Families with Novel Variants in HPS3 and HPS4 Genes. Genes 14 (1) (2023)
Hayat Alameen Ali, Osama Yousef Muthaffar, Nahla AlKarim, Husam Kayyali, Ahmed Elmardenly, Abdullah Tamim, Hala Alansari
The efficacy of non-fasting ketogenic diet protocol in the management of intractable epilepsy in pediatric patients: a single center study from Saudi Arabia. The Journal of international medical research 50 (3) (2022)
Osama Yousef Muthaffar
Brain Magnetic Resonance Imaging Findings in Infantile Spasms. Neurology international 14 (1) (2022)