Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Ahmed Al‐Rumayyan"'
Autor:
Ahlam Ahmed Abu Melha, Amjad Saad Aldress, Fahad Alamri, Lama Saleh Aljomah, Raid Hommady, Ahmed Al-Rumayyan, Fahad Albassam
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
IntroductionThe last few decades have increased our understanding of autoimmune encephalitis (AE). In both the pediatric and adult populations, it proves to be a disease of dramatic acute onset of heterogeneous clinical manifestations, notably enceph
Externí odkaz:
https://doaj.org/article/46a85ef0975548dc97ae99b1c5edaec3
Autor:
Muhammad Umair, Muhammad Farooq Khan, Mohammed Aldrees, Marwan Nashabat, Kheloud M. Alhamoudi, Muhammad Bilal, Yusra Alyafee, Abeer Al Tuwaijri, Manar Aldarwish, Ahmed Al-Rumayyan, Hamad Alkhalaf, Mohammad A. M. Wadaan, Majid Alfadhel
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Von Willebrand A domain-containing protein 8 (VWA8), also named KIAA0564, is a poorly characterized, mitochondrial matrix-targeted protein having a putative ATPase activity. VWA8 is comprising of ATPase-associated domains and a VWFA domain associated
Externí odkaz:
https://doaj.org/article/363b2eec6410403fb8e787f0d6ca8e8b
Autor:
Majid Alfadhel, Muhammad Umair, Bader Almuzzaini, Saif Alsaif, Sulaiman A. AlMohaimeed, Maher A. Almashary, Wardah Alharbi, Latifah Alayyar, Abdulrahman Alasiri, Mariam Ballow, Abdulkareem AlAbdulrahman, Monira Alaujan, Marwan Nashabat, Ali Al‐Odaib, Waleed Altwaijri, Ahmed Al‐Rumayyan, Muhammad T. Alrifai, Ahmed Alfares, Mohammed AlBalwi, Brahim Tabarki
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 10, Pp 2097-2103 (2019)
Abstract Background Biotin–thiamine‐responsive basal ganglia disease (BTBGD) is an autosomal recessive neurometabolic disorder mostly presented in children. The disorder is described as having subacute encephalopathy with confusion, dystonia, and
Externí odkaz:
https://doaj.org/article/96e539f8f7c14fda9b2b9706c9f85dd7
Publikováno v:
Journal of Biochemical and Clinical Genetics, Vol 2, Iss 1, Pp 85-90 (2019)
Background: Familial hemiplegic migraine (FHM) is a rare disorder presented commonly with coma, hyperthermia, and headache. FHM is usually associated with fully reversible motor weakness as a specific symptom of aura. Seizure and fever are the second
Externí odkaz:
https://doaj.org/article/a957073d984443a39a4c5edfeaf91692
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
Autor:
Muhammad Umair, Muhammad Farooq Khan, Mohammed Aldrees, Marwan Nashabat, Kheloud M. Alhamoudi, Muhammad Bilal, Yusra Alyafee, Abeer Al Tuwaijri, Manar Aldarwish, Ahmed Al-Rumayyan, Hamad Alkhalaf, Mohammad A. M. Wadaan, Majid Alfadhel
Publikováno v:
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Von Willebrand A domain-containing protein 8 (VWA8), also named KIAA0564, is a poorly characterized, mitochondrial matrix-targeted protein having a putative ATPase activity. VWA8 is comprising of ATPase-associated domains and a VWFA domain associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9772d222bf013123ce0e24d668571c3
https://pubmed.ncbi.nlm.nih.gov/34660594
https://pubmed.ncbi.nlm.nih.gov/34660594
Autor:
Hanin Al-Gethami, Ahmed Al-Rumayyan, Waleed Altuwaijri, Duaa Ba-Armah, Talal Alrifai Muhammad
Publikováno v:
Neurosciences
Objectives: To estimate the prevalence and characteristics of headache in pediatric epileptic patients. Methods: This cross-sectional study was performed over 6 months period from January 2018 to June 2018 at King Abdullah Specialist Children Hospita
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5bfca846e19f69303c4456bd5c15e40
https://doi.org/10.17712/nsj.2019.4.20190043
https://doi.org/10.17712/nsj.2019.4.20190043
Autor:
Cristina Skrypnyk, Abubaker Al Madani, Mohammed Jan, André Mégarbané, Khalid Al Thihli, Ali Al Shehri, Abdulaziz Al Saman, Mohammad Al Muhaizea, Waseem Fathalla, Andoni Urtizberea, Gholamreza Zamani, Sylvie Tuffery-Giraud, Carlos Ignacio Ortez González, Pawan Kashyape, Ahmed Al Rumayyan, Edward Cupler, Laila Bastaki, Mohammed Al Jumah, Gururaj Aithala Kodavooru
Publikováno v:
Neurodegenerative Disease Management
Aim: Duchenne muscular dystrophy (DMD) is a severe and rare X-linked neuromuscular childhood disorder that results in functional decline, loss of ambulation and early death due to cardiac or respiratory failure. The objective of this paper is to addr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2083e73b42e1499b6778e9dd983e38a
https://doi.org/10.2217/nmt-2019-0002
https://doi.org/10.2217/nmt-2019-0002
Autor:
Waleed Altuwaijri, Hanin Al-Gethami, Mohammad Talal Alrifai, Ahmed Al-Rumayyan, Duaa Ba-Armah
Publikováno v:
International Neuropsychiatric Disease Journal. :1-10
Subacute sclerosing panencephalitis (SSPE) is a progressive degenerative disease caused by measles infection with overall poor prognosis in spite multiple modalities of treatment. The course of the disease is characterized by progressive neurological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d0cd9cac5a56eba0264dc1da0ef913e
https://doi.org/10.9734/indj/2019/v13i130101
https://doi.org/10.9734/indj/2019/v13i130101
Autor:
Abdulaziz H. Alhaqbani, Waleed Altuwaijri, Mohammed M. Altuwaijri, Nawaf A. Alharthi, Bander Ali Aldamkh, Muhammad Talal Alrifai, Abdalaziz F. Alamer, Ahmed Al-Rumayyan, Saeed A. Aldamkh, Mohammed A. Alrumayyan, Amjad S. Aldrees
Publikováno v:
Neurosciences. 24:89-94
Objective To evaluate the clinical presenation of acute disseminated Encephalomyelitis (ADEM) in pediatric age group, treatments, and to asses the outcome at King Abdulaziz Medical City, Riyadh, Kingdom of Saudia Arabia. Methods The medical records o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::802a1fde34b564b8725983c272d10484
https://doi.org/10.17712/nsj.2019.2.20180017
https://doi.org/10.17712/nsj.2019.2.20180017