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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 2
2005 4
2006 5
2007 10
2008 8
2009 4
2010 3
2011 3
2012 6
2013 7
2014 4
2015 2
2016 4
2017 3
2018 3
2019 4
2020 7
2021 1
2022 7
2023 12
2024 3

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90 results

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Page 1
The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families.
Al-Kasbi G, Al-Murshedi F, Al-Kindi A, Al-Hashimi N, Al-Thihli K, Al-Saegh A, Al-Futaisi A, Al-Mamari W, Al-Asmi A, Bruwer Z, Al-Kharusi K, Al-Rashdi S, Zadjali F, Al-Yahyaee S, Al-Maawali A. Al-Kasbi G, et al. Among authors: al futaisi a. Sci Rep. 2022 Nov 7;12(1):18862. doi: 10.1038/s41598-022-22036-z. Sci Rep. 2022. PMID: 36344539 Free PMC article.
TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia.
Tábara LC, Al-Salmi F, Maroofian R, Al-Futaisi AM, Al-Murshedi F, Kennedy J, Day JO, Courtin T, Al-Khayat A, Galedari H, Mazaheri N, Protasoni M, Johnson M, Leslie JS, Salter CG, Rawlins LE, Fasham J, Al-Maawali A, Voutsina N, Charles P, Harrold L, Keren B, Kunji ERS, Vona B, Jelodar G, Sedaghat A, Shariati G, Houlden H, Crosby AH, Prudent J, Baple EL. Tábara LC, et al. Among authors: al futaisi am. Brain. 2022 Sep 14;145(9):3095-3107. doi: 10.1093/brain/awac123. Brain. 2022. PMID: 35718349 Free PMC article.
Diabesity in the Arabian Gulf: Challenges and Opportunities.
Khalil AB, Beshyah SA, Abdella N, Afandi B, Al-Arouj MM, Al-Awadi F, Benbarka M, Ben Nakhi A, Fiad TM, Al Futaisi A, Hassoun AA, Hussein W, Kaddaha G, Ksseiry I, Al Lamki M, Madani AA, Saber FA, Abdel Aal Z, Morcos B, Saadi H. Khalil AB, et al. Among authors: al futaisi a. Oman Med J. 2018 Jul;33(4):273-282. doi: 10.5001/omj.2018.53. Oman Med J. 2018. PMID: 30038726 Free PMC article. Review. No abstract available.
Absent Septum Pellucidum: Search for other anomalies.
Saleh K, Al-Ajmi E, Al Futaisi A. Saleh K, et al. Among authors: al futaisi a. Sultan Qaboos Univ Med J. 2023 Aug;23(3):423-424. doi: 10.18295/squmj.5.2023.024. Epub 2023 Aug 28. Sultan Qaboos Univ Med J. 2023. PMID: 37655086 Free PMC article. No abstract available.
Telemedicine in the Era of COVID-19 and Beyond: A new horizon.
Alsaffar H, Almamari W, Al Futaisi A. Alsaffar H, et al. Among authors: al futaisi a. Sultan Qaboos Univ Med J. 2020 Nov;20(4):e277-e279. doi: 10.18295/squmj.2020.20.04.001. Epub 2020 Dec 21. Sultan Qaboos Univ Med J. 2020. PMID: 33414930 Free PMC article. No abstract available.
PLPHP deficiency: clinical, genetic, biochemical, and mechanistic insights.
Johnstone DL, Al-Shekaili HH, Tarailo-Graovac M, Wolf NI, Ivy AS, Demarest S, Roussel Y, Ciapaite J, van Roermund CWT, Kernohan KD, Kosuta C, Ban K, Ito Y, McBride S, Al-Thihli K, Abdelrahim RA, Koul R, Al Futaisi A, Haaxma CA, Olson H, Sigurdardottir LY, Arnold GL, Gerkes EH, Boon M, Heiner-Fokkema MR, Noble S, Bosma M, Jans J, Koolen DA, Kamsteeg EJ, Drögemöller B, Ross CJ, Majewski J, Cho MT, Begtrup A, Wasserman WW, Bui T, Brimble E, Violante S, Houten SM, Wevers RA, van Faassen M, Kema IP, Lepage N; Care4Rare Canada Consortium; Lines MA, Dyment DA, Wanders RJA, Verhoeven-Duif N, Ekker M, Boycott KM, Friedman JM, Pena IA, van Karnebeek CDM. Johnstone DL, et al. Among authors: al futaisi a. Brain. 2019 Mar 1;142(3):542-559. doi: 10.1093/brain/awy346. Brain. 2019. PMID: 30668673 Free PMC article.
90 results