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

Year Number of Results
1998 3
1999 1
2002 1
2003 3
2004 2
2005 5
2006 7
2007 6
2008 1
2009 3
2010 5
2011 7
2012 6
2013 11
2014 9
2015 9
2016 6
2017 7
2018 5
2019 10
2020 16
2021 19
2022 13
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Search Results

136 results
Results by year
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Page 1
COVID-19 and the ABO blood group connection.
Zaidi FZ, Zaidi ARZ, Abdullah SM, Zaidi SZA. Zaidi FZ, et al. Among authors: abdullah sm. Transfus Apher Sci. 2020 Oct;59(5):102838. doi: 10.1016/j.transci.2020.102838. Epub 2020 Jun 3. Transfus Apher Sci. 2020. PMID: 32513613 Free PMC article. No abstract available.
Rapid spread of SARS-CoV-2 Omicron subvariant BA.2 in a single-source community outbreak.
Cheng VC, Ip JD, Chu AW, Tam AR, Chan WM, Abdullah SMU, Chan BP, Wong SC, Kwan MY, Chua GT, Ip P, Chan JM, Lam BH, To WK, Chuang VW, Yuen KY, Hung IF, To KK. Cheng VC, et al. Among authors: abdullah smu. Clin Infect Dis. 2022 Mar 10:ciac203. doi: 10.1093/cid/ciac203. Online ahead of print. Clin Infect Dis. 2022. PMID: 35271728 Free PMC article.
Time to administration of antibiotics and mortality in sepsis.
Siewers K, Abdullah SMOB, Sørensen RH, Nielsen FE. Siewers K, et al. Among authors: abdullah smob. J Am Coll Emerg Physicians Open. 2021 May 13;2(3):e12435. doi: 10.1002/emp2.12435. eCollection 2021 Jun. J Am Coll Emerg Physicians Open. 2021. PMID: 34027515 Free PMC article.
Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome.
Pottie L, Adamo CS, Beyens A, Lütke S, Tapaneeyaphan P, De Clercq A, Salmon PL, De Rycke R, Gezdirici A, Gulec EY, Khan N, Urquhart JE, Newman WG, Metcalfe K, Efthymiou S, Maroofian R, Anwar N, Maqbool S, Rahman F, Altweijri I, Alsaleh M, Abdullah SM, Al-Owain M, Hashem M, Houlden H, Alkuraya FS, Sips P, Sengle G, Callewaert B. Pottie L, et al. Among authors: abdullah sm. Am J Hum Genet. 2021 Dec 2;108(12):2386-2388. doi: 10.1016/j.ajhg.2021.11.009. Am J Hum Genet. 2021. PMID: 34861177 Free PMC article. No abstract available.
Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome.
Pottie L, Adamo CS, Beyens A, Lütke S, Tapaneeyaphan P, De Clercq A, Salmon PL, De Rycke R, Gezdirici A, Gulec EY, Khan N, Urquhart JE, Newman WG, Metcalfe K, Efthymiou S, Maroofian R, Anwar N, Maqbool S, Rahman F, Altweijri I, Alsaleh M, Abdullah SM, Al-Owain M, Hashem M, Houlden H, Alkuraya FS, Sips P, Sengle G, Callewaert B. Pottie L, et al. Among authors: abdullah sm. Am J Hum Genet. 2021 Jun 3;108(6):1095-1114. doi: 10.1016/j.ajhg.2021.04.016. Epub 2021 May 14. Am J Hum Genet. 2021. PMID: 33991472 Free PMC article.
136 results