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

Year Number of Results
1990 1
1991 3
1992 2
1995 1
1996 1
1997 2
1998 1
1999 4
2000 1
2001 2
2002 3
2004 1
2005 1
2006 4
2007 3
2008 1
2009 2
2010 7
2011 4
2012 4
2013 4
2014 4
2015 3
2016 5
2017 4
2018 9
2019 2
2020 1
2021 4
2022 4
2023 1
2024 0

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85 results

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Page 1
Multicoagulant resistant pseudothrombocytopenia.
Waseem N, Hanif B, Jabbar J. Waseem N, et al. J Pak Med Assoc. 2021 Sep;71(9):2247-2249. doi: 10.47391/JPMA.03-390. J Pak Med Assoc. 2021. PMID: 34580523 Free article.
Acceptance.
Waseem N. Waseem N. Palliat Support Care. 2016 Aug;14(4):445-8. doi: 10.1017/S147895151500111X. Epub 2015 Sep 16. Palliat Support Care. 2016. PMID: 26373924 No abstract available.
Hypoxic Hepatitis: A Review and Clinical Update.
Waseem N, Chen PH. Waseem N, et al. J Clin Transl Hepatol. 2016 Sep 28;4(3):263-268. doi: 10.14218/JCTH.2016.00022. Epub 2016 Sep 7. J Clin Transl Hepatol. 2016. PMID: 27777895 Free PMC article. Review.
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development.
Simcoe MJ, Shah A, Fan B, Choquet H, Weisschuh N, Waseem NH, Jiang C, Melles RB, Ritch R, Mahroo OA, Wissinger B, Jorgenson E, Wiggs JL, Garway-Heath DF, Hysi PG, Hammond CJ. Simcoe MJ, et al. Among authors: waseem nh. Ophthalmology. 2022 Jun;129(6):626-636. doi: 10.1016/j.ophtha.2022.01.005. Epub 2022 Jan 11. Ophthalmology. 2022. PMID: 35031440 Free article.
Mutations in SPATA13/ASEF2 cause primary angle closure glaucoma.
Waseem NH, Low S, Shah AZ, Avisetti D, Ostergaard P, Simpson M, Niemiec KA, Martin-Martin B, Aldehlawi H, Usman S, Lee PS, Khawaja AP, Ruddle JB, Shah A, Sackey E, Day A, Jiang Y, Swinfield G, Viswanathan A, Alfano G, Chakarova C, Cordell HJ, Garway-Heath DF, Khaw PT, Bhattacharya SS, Waseem A, Foster PJ. Waseem NH, et al. PLoS Genet. 2020 Apr 27;16(4):e1008721. doi: 10.1371/journal.pgen.1008721. eCollection 2020 Apr. PLoS Genet. 2020. PMID: 32339198 Free PMC article.
A clinical and molecular characterisation of CRB1-associated maculopathy.
Khan KN, Robson A, Mahroo OAR, Arno G, Inglehearn CF, Armengol M, Waseem N, Holder GE, Carss KJ, Raymond LF, Webster AR, Moore AT, McKibbin M, van Genderen MM, Poulter JA, Michaelides M; UK Inherited Retinal Disease Consortium. Khan KN, et al. Among authors: waseem n. Eur J Hum Genet. 2018 May;26(5):687-694. doi: 10.1038/s41431-017-0082-2. Epub 2018 Feb 1. Eur J Hum Genet. 2018. PMID: 29391521 Free PMC article.
85 results