Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Khalid, Hundallah"'
Autor:
Raid Hommady, Abdullah Alsohibani, Ruba Alayed, Abdulaziz Alshehri, Ahlam AbuMelha, Lama Aljomah, Khalid Hundallah, Mohammed Almuqbil, Waleed Altuwaijri, Ahmad Alrumayyan, Muhammad Talal Alrifai, Duaa Mohammed Baarmah
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-6 (2023)
Abstract Background Anti-N-methyl-d-aspartate “anti-NMDA” receptor encephalitis is one of the most common autoimmune encephalitis for which first- and second-line therapies have been recommended following international consensus. However, some re
Externí odkaz:
https://doaj.org/article/f0964a37ba044f55af717a7ac0ea6d7f
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
The neurological complications of coronavirus disease 2019 (COVID-19) can range from simple tremors and dystonia to features of encephalopathy. Toll-like receptor 7 (TLR7) belongs to a family of innate immune receptors responsible for viral RNA detec
Externí odkaz:
https://doaj.org/article/e7764d1fcc2f43a6a98f9c92704c992b
Autor:
Majid Alfadhel, Mohammed Almuqbil, Fuad Al Mutairi, Muhammad Umair, Mohammed Almannai, Malak Alghamdi, Hamad Althiyab, Rayyan Albarakati, Fahad A. Bashiri, Walaa Alshuaibi, Duaa Ba-Armah, Mohammed A. Saleh, Ali Al-Asmari, Eissa Faqeih, Waleed Altuwaijri, Ahmed Al-Rumayyan, Mohammed Ali Balwi, Faroug Ababneh, Abdulrahman Faiz Alswaid, Wafaa M. Eyaid, Naif A. M. Almontashiri, Amal Alhashem, Khalid Hundallah, Aida Bertoli-Avella, Peter Bauer, Christian Beetz, Muhammad Talal Alrifai, Ahmed Alfares, Brahim Tabarki
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background: Leukodystrophies (LDs) are inherited heterogeneous conditions that affect the central nervous system with or without peripheral nerve involvement. They are individually rare, but collectively, they are common. Thirty disorders were includ
Externí odkaz:
https://doaj.org/article/16784d501eb142d69ee3665c6c73dd51
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Novel therapeutic strategies have shown some promise in treating spinal muscular atrophy (SMA). However, the outcomes and acceptance of these new strategies are yet to be explored. We aimed to investigate physicians' opinions and perceptions toward m
Externí odkaz:
https://doaj.org/article/ae47506a607a4297bd2aef5a626cd262
Autor:
Hanin Alsini, Abdulaziz Alghamdi, Shatha Alshafi, Khalid Hundallah, Sameer Almehmadi, Daad Alsowat, Suad Al-Yamani, Hanin Almuzaini, Ali Alwadie, Ali Al-Otaibi, Lamyaa Jad, Asma Almadhi, Fahad Bashiri, Amal Kentab, Muddathir H Hamad, Duaa Baarmah, Mohammed Alrifaie, Mohammed Almuqbel, Raidah Al Baradie, Ali Mir, Mohammed Jan, Osama Muthaffar, Mohammed Aljabri, Elsayed Ali, Mohammed Saeed, Abeer Matar, Brahim Tabarki
Publikováno v:
Seizure. 107:146-154
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:
Fahad A. Bashiri, Sultan Al Johani, Muddathir H. Hamad, Amal Y. Kentab, Ali H. Alwadei, Khalid Hundallah, Hamdi H. Hasan, Walaa Alshuaibi, Lamyaa Jad, Muhammad Talal Alrifai, Abrar Hudairi, Rana Al Sheikh, Asma'a Alenizi, Nawaf A. Alharthi, Tayseer A. Abdelmagid, Duaa Ba-Armah, Mustafa A. Salih, Brahim Tabarki
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Background: Acute necrotizing encephalopathy of childhood (ANEC) is a rapidly progressing encephalopathy characterized by fever, depressed level of consciousness, and seizures. Diagnosis depends on clinical presentation and characteristic neuroimagin
Externí odkaz:
https://doaj.org/article/f60dfa80ad47449f84dc3275ddfebaba
Autor:
Amal, Aldhilan, Afnan, Alhakeem, Sumayah, Al Hajjaj, Musaad, Abukhalid, Hisham, Aldhalaan, Ehab, Salah, Muhammed, Saeed, Sadia, Tabassum, Heba Y, El Khashab, Mohammed, Aljabri, El-Sayed, Ali, Ali, Alwadei, Khalid, Hundallah, Abdulaziz, Alghamdi, Wejdan, Hakami, Shatha, AlShafi, Fowzan S, Alkuraya, Naif, Alanazy, Mohammed Zain, Seidahmed, Majid, Alfadhel, Brahim, Tabarki
Publikováno v:
Pediatric Neurology. 134:78-82
Hyperekplexia is a rare disorder characterized by exaggerated startle responses to unexpected sensory stimuli, recurrent apneas, and stiffness. Only few studies have been published on this disorder in populations with high rates of consanguinity.We r
Autor:
Musaad Abukhaled, Mohammed Al Muqbil, Malak Ali Alghamdi, Khalid Hundallah, Jehan Suleiman, Tawfeg Ben-Omran, Majid Alfadhel, Mohammed Almannai, Rehab Alsaleh, Brahim Tabarki
Publikováno v:
European Journal of Pediatrics.
Autor:
Musaad Abukhaled, Mohammed Al Muqbil, Malak Ali Alghamdi, Khalid Hundallah, Jehan Suleiman, Tawfeg Ben-Omran, Majid Alfadhel, Mohammed Almannai, Rehab Alsaleh, Brahim Tabarki
Publikováno v:
European Journal of Pediatrics.
Aromatic L-amino acid decarboxylase (AADC) deficiency is a rare inherited neurometabolic disorder that can lead to severe physical and developmental impairment. This report includes 16 patients from the Middle East and is the largest series of patien