Zobrazeno 1 - 10
of 90
pro vyhledávání: '"A. Alakkas"'
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 41, Iss , Pp 101135- (2024)
L-2 hydroxyglutaric aciduria (L-2-HGA) is a rare autosomal recessive progressive, organic aciduria which presents with a wide variety of clinical manifestations. Diagnosis is complex and necessitates an increase in clinical suspicion of the disease t
Externí odkaz:
https://doaj.org/article/39acf8dad0614f4db4eb65b8f99fe8ed
Publikováno v:
Therapeutics and Clinical Risk Management, Vol Volume 19, Pp 1019-1024 (2023)
Samuel Frank,1 Aljoharah Alakkas2 1Department of Neurology, Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, MA, USA; 2Department of Neurology, National Neuroscience Institute, King Fahad Medical City, Riyadh, K.S.ACorrespondence:
Externí odkaz:
https://doaj.org/article/d7ee357fcd8c4b788aebc044007c0b46
Autor:
Alakkas, Ziyad1 (AUTHOR) Alakkas.ziyad@gmail.com, Gari, Abdulaziz M.2 (AUTHOR), Makhdoum, Sara3 (AUTHOR), AlSindi, Eman A.2 (AUTHOR)
Publikováno v:
Journal of Medical Case Reports. 5/1/2024, Vol. 18 Issue 1, p1-8. 8p.
Autor:
Alakkas, Abdullah Abdurhman1, Alhumoudi, Hamad1, Khan, Hina2, Imam, Ashraf3, Khatoon, Asma4, Bashir, Samina5, Khan, Imran Ahmad5
Publikováno v:
Corporate Governance & Organizational Behavior Review. 2024, Vol. 8 Issue 2, p93-102. 10p.
Akademický článek
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Autor:
Khan, Mohammed Arshad1 m.akhan@seu.edu.sa, Alakkas, Abdullah A.2 a.alakkas@seu.edu.sa, Khojah, Maysoon2 m.khoja@seu.edu.sa, Vivek3 vivek@jmi.ac.in, Alhumoudi, Hamad2 h.alhumoudi@seu.edu.sa
Publikováno v:
International Journal of Professional Business Review (JPBReview). 2023, Vol. 8 Issue 11, p1-26. 26p.
Autor:
Katherine Longardner, Brenton A Wright, Aljoharah Alakkas, Hyeri You, Ronghui Xu, Lin Liu, Fatta B Nahab
Publikováno v:
PLoS ONE, Vol 18, Iss 1, p e0278262 (2023)
BackgroundParkinson disease (PD) psychosis (PDP) is a disabling non-motor symptom. Pharmacologic treatment is limited to pimavanserin, quetiapine, and clozapine, which do not worsen parkinsonism. A Food and Drug Administration black box warning exist
Externí odkaz:
https://doaj.org/article/5002053154824691ac7683516e7829b3
Publikováno v:
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-7 (2021)
Abstract Background Behçet’s syndrome is a type of systemic chronic vasculitis of unknown etiology, frequently characterized by recurrent oral and genital ulcers and uveitis. It is less commonly characterized by arthritis and skin, vascular, and g
Externí odkaz:
https://doaj.org/article/0a7ff22fda4b40ec963f6e007c3e7999
Publikováno v:
International Journal of General Medicine, Vol Volume 14, Pp 505-514 (2021)
Abdulrahman AlQahtani,1 Ziyad Alakkas,1 Fayez Althobaiti,1 Mohammed Alosaimi,1 Baraa Abuzinadah,1 Elshazly Abdulkhalik,2,3 Khaled Alswat4 1Internal Medicine Department, King Abdul Aziz Specialist Hospital, Taif, Makkah, Saudi Arabia; 2Consultant Card
Externí odkaz:
https://doaj.org/article/24500de5d41d4b78a150457de3556ba3
Autor:
Alhumoudi, Hamad, Alakkas, Abdullah Abdurhman, Khan, Soha, Imam, Ashraf, Baig, Asif, Omer, Adam Mohamed, Khan, Imran Ahmad
Publikováno v:
International Journal of Sustainable Development & Planning; May2024, Vol. 19 Issue 5, p1971-1979, 9p