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

Year Number of Results
2001 3
2002 5
2005 1
2006 2
2007 1
2009 1
2010 1
2011 1
2014 3
2015 1
2016 1
2017 4
2018 1
2020 1
2021 2
2024 0

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26 results

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Page 1
COVID-19 versus SARS: A comparative review.
Keshta AS, Mallah SI, Al Zubaidi K, Ghorab OK, Keshta MS, Alarabi D, Abousaleh MA, Salman MT, Taha OE, Zeidan AA, Elsaid MF, Tang P. Keshta AS, et al. Among authors: elsaid mf. J Infect Public Health. 2021 Jul;14(7):967-977. doi: 10.1016/j.jiph.2021.04.007. Epub 2021 Apr 24. J Infect Public Health. 2021. PMID: 34130121 Free PMC article. Review.
Gene therapy for spinal muscular atrophy: the Qatari experience.
Ali HG, Ibrahim K, Elsaid MF, Mohamed RB, Abeidah MIA, Al Rawwas AO, Elshafey K, Almulla H, El-Akouri K, Almulla M, Othman A, Musa S, Al-Mesaifri F, Ali R, Shahbeck N, Al-Mureikhi M, Alsulaiman R, Alkaabi S, Ben-Omran T. Ali HG, et al. Among authors: elsaid mf. Gene Ther. 2021 Nov;28(10-11):676-680. doi: 10.1038/s41434-021-00273-7. Epub 2021 Jul 19. Gene Ther. 2021. PMID: 34276047 Free PMC article.
Neuro-brucellosis in children.
Bessisso MS, Elsaid MF, Elshazli SS, Abdelrahman HM, Alali MG, Ali AR, Aljaber HM. Bessisso MS, et al. Among authors: elsaid mf. Neurosciences (Riyadh). 2001 Jan;6(1):67-9. Neurosciences (Riyadh). 2001. PMID: 24185230
Mutation in noncoding RNA RNU12 causes early onset cerebellar ataxia.
Elsaid MF, Chalhoub N, Ben-Omran T, Kumar P, Kamel H, Ibrahim K, Mohamoud Y, Al-Dous E, Al-Azwani I, Malek JA, Suhre K, Ross ME, Aleem AA. Elsaid MF, et al. Ann Neurol. 2017 Jan;81(1):68-78. doi: 10.1002/ana.24826. Ann Neurol. 2017. PMID: 27863452
Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients' cohort from Qatar. A population specific founder variant.
Abdel Aleem A, Elsaid MF, Chalhoub N, Chakroun A, Mohamed KAS, AlShami R, Kuzu O, Mohamed RB, Ibrahim K, AlMudheki N, Osman O, Ross ME, ELalamy O. Abdel Aleem A, et al. Among authors: elsaid mf. Neuromuscul Disord. 2020 Jun;30(6):457-471. doi: 10.1016/j.nmd.2020.03.009. Epub 2020 Apr 17. Neuromuscul Disord. 2020. PMID: 32444167
Recurrence risk after a first febrile convulsion.
Bessisso MS, Elsaid MF, Almula NA, Kadomi NK, Zeidan SH, Azzam SB, Swied HA, Shahbiek NI, Abuhazemma KJ, Abu-Shahin AM, Alkhalaf FA. Bessisso MS, et al. Among authors: elsaid mf. Saudi Med J. 2001 Mar;22(3):254-8. Saudi Med J. 2001. PMID: 11307113
Autosomal recessive inheritance of GLUT1 deficiency syndrome.
Klepper J, Scheffer H, Elsaid MF, Kamsteeg EJ, Leferink M, Ben-Omran T. Klepper J, et al. Among authors: elsaid mf. Neuropediatrics. 2009 Oct;40(5):207-10. doi: 10.1055/s-0030-1248264. Epub 2010 Mar 10. Neuropediatrics. 2009. PMID: 20221955
26 results