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Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report.
Al Mutairi F, Alkhalaf R, Alkhorayyef A, Alroqi F, Yusra A, Umair M, Nouf F, Khan A, Meshael A, Hamad A, Monira A, Asiri A, Alhamoudi KM, Alfadhel M. Al Mutairi F, et al. BMC Pulm Med. 2020 May 15;20(1):141. doi: 10.1186/s12890-020-1175-1. BMC Pulm Med. 2020. PMID: 32414360 Free PMC article.
Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay.
Asiri A, Aloyouni E, Umair M, Alyafee Y, Al Tuwaijri A, Alhamoudi KM, Almuzzaini B, Al Baz A, Alwadaani D, Nashabat M, Alfadhel M. Asiri A, et al. Ann Clin Transl Neurol. 2020 Jun;7(6):956-964. doi: 10.1002/acn3.51059. Epub 2020 May 19. Ann Clin Transl Neurol. 2020. PMID: 32431071 Free PMC article.
Measuring public awareness about blood donation in Assir, South-Western Saudi Arabia.
Otifi HM, Asiri MA, Ahmad MT, Asiri AA, AlOudhah SM, Alshorfy HA, Alalmai AM, Alam MM. Otifi HM, et al. Among authors: asiri aa. Transfus Clin Biol. 2020 Jun 16:S1246-7820(20)30079-3. doi: 10.1016/j.tracli.2020.06.005. Online ahead of print. Transfus Clin Biol. 2020. PMID: 32561325
Quality of life assessment among multiple sclerosis patients in Saudi Arabia.
Alhazzani AA, Alqahtani MS, Alahmari MS, Asiri MA, Alamri NM, Sarhan LA, Alkhashrami SS, Asiri AA. Alhazzani AA, et al. Among authors: asiri aa. Neurosciences (Riyadh). 2018 Apr;23(2):140-147. doi: 10.17712/nsj.2018.2.20170335. Neurosciences (Riyadh). 2018. PMID: 29664456
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