Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Osama Y. Muthaffar"'
Autor:
Imad M. Khojah, Osama Y. Muthaffar, Anas S. Alyazidi, Maha K. Alghamdi, Mayar M. Salem, Hassan A. Alalawi, Ohud T. Alharbi, Latifa A. Almuharib
Publikováno v:
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 60, Iss 1, Pp 1-7 (2024)
Abstract Background COVID-19 is a global pandemic that has highly impacted the healthcare system and patients, especially patients with epilepsy, due to the fact that the success of their treatment depends on obtaining sustainable access to medical p
Externí odkaz:
https://doaj.org/article/06bf093589f64400a668e81d68711fa7
Autor:
Osama Y. Muthaffar, Anas S. Alyazidi, Daad Alsowat, Abdulaziz A. Alasiri, Raidah Albaradie, Lamyaa A. Jad, Husam Kayyali, Mohammed M. S. Jan, Ahmed K. Bamaga, Mohammed A. Alsubaie, Rawan Daghistani, Saleh S. Baeesa, Meshari A. Alaifan, Abdelhakim Makraz, Abrar N. Alsharief, Muhammad Imran Naseer
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
BackgroundDrug-resistant epilepsy (DRE) impacts a significant portion, one-third, of individuals diagnosed with epilepsy. In such cases, exploring non-pharmacological interventions are crucial, with the ketogenic diet (KD) standing out as a valuable
Externí odkaz:
https://doaj.org/article/647b88ed8e58452592e36172167ec537
Autor:
Mohammed A. Almuqbil, Sadia Tabassum, Osama Y. Muthaffar, Fouad Ghamdi, Zainab Al Masseri, Abdulaziz Alsaman, Reem A. Alkhater
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 4, Pp 1063-1066 (2024)
Abstract Parkinsonism‐dystonia‐2 PKDYS2 is an autosomal‐recessive disorder, caused by pathogenic biallelic variants in SLC18A2 which encodes the vesicular monoamine transporter (VMAT2) protein. PKDYS2 is a treatable neurotransmitter disease, an
Externí odkaz:
https://doaj.org/article/83da58cca01a4c668679c34f9adbe6b6
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundThe mitochondria are a cellular power house. Tissues are involved in frequent energy consumption, and any failure or irregularity in the continuous energy production could lead to abnormalities. The leucine-rich pentatricopeptide repeat (LR
Externí odkaz:
https://doaj.org/article/616f74d76e8c4332a85037d9ccb8f10b
Autor:
Osama Y. Muthaffar
Publikováno v:
Neurology International, Vol 14, Iss 1, Pp 261-270 (2022)
Background: Infantile spasms are an age-specific epileptic disorder. They occur in infancy and early childhood. They can be caused by multiple etiologies. Structural abnormalities represent an important cause of infantile spasms. Brain magnetic reson
Externí odkaz:
https://doaj.org/article/9d8c3bddaad645008d7e9e7e89b4ed2b
Publikováno v:
Biomedicines, Vol 11, Iss 9, p 2402 (2023)
Background: The seizure threshold 2 (SZT2) gene encodes a protein of unknown function, which is widely expressed, confers a low seizure threshold, and enhances epileptogenesis. It also comprises the KICSTOR protein complex, which inhibits the mTORC1
Externí odkaz:
https://doaj.org/article/d28e605c92204c8d9cebead4ffff3b86
Autor:
Muhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Peter Natesan Pushparaj, Samah Saharti, Osama Y. Muthaffar
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Leukodystrophies are a diverse group of genetically established disorders categorized by unusual white matter changes on brain imaging. Hypomyelinating leukodystrophies (HLDs) are a group of neurodevelopmental disorders that affect myelin sheath deve
Externí odkaz:
https://doaj.org/article/db3ec61e9bf844f9b1ab3e5227423a5e
Autor:
Muhammad Imran Naseer, Peter Natesan Pushparaj, Angham Abdulrahman Abdulkareem, Osama Y. Muthaffar
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2022)
Biotinidase deficiency is an autosomal recessive, multiple carboxylase deficiency usually associated with seizures, eczema, hypotonia, visual disturbances, hearing loss, and developmental delays. Only a handful of cases of biotinidase deficiency that
Externí odkaz:
https://doaj.org/article/8029b5eccf984ffbb954b360352fe5cc
Autor:
Ahmed K. Bamaga, Fouad Alghamdi, Nahla Alshaikh, Waleed Altwaijri, Fahad A. Bashiri, Khalid Hundallah, Musaad Abukhaled, Osama Y. Muthaffar, Sameer Al-Mehmadi, Tahani Ahmed Jamaly, Mohammad A. Al-Muhaizea, Abdulaziz Al-Saman
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background: The coronavirus disease 2019 (COVID-19) pandemic has caused overwhelming challenges in healthcare worldwide. During such an outbreak, some needs of high-risk groups who require regular follow-ups and long-term management are not met. The
Externí odkaz:
https://doaj.org/article/7afbdcab69a64029b4233f05a7e46459
Autor:
Anas S Alyazidi, Osama Y Muthaffar, Fahad A Alotibi, Albatool Almubarak, Luca Tamai, Siba Z Takieddin, Maha Alghamdi, Yara K Alraddadi
Publikováno v:
Cureus. 14(10)
Introduction The social acceptance of patients with epilepsy is largely determined by society's opinion of epilepsy; therefore, individuals with epilepsy could face prejudice and stigma as a result of negative impressions. Religious beliefs and mysti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3c301d047ba68e936ca51309d99f8d9
https://pubmed.ncbi.nlm.nih.gov/36381863
https://pubmed.ncbi.nlm.nih.gov/36381863