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

Year Number of Results
2000 1
2001 1
2003 5
2004 1
2005 1
2006 2
2007 1
2008 1
2009 1
2010 3
2011 4
2012 3
2013 2
2014 1
2015 3
2016 4
2017 1
2018 2
2020 1
2021 3
2022 3
2023 2
2024 4

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42 results

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Page 1
Differentiating drusen: Drusen and drusen-like appearances associated with ageing, age-related macular degeneration, inherited eye disease and other pathological processes.
Khan KN, Mahroo OA, Khan RS, Mohamed MD, McKibbin M, Bird A, Michaelides M, Tufail A, Moore AT. Khan KN, et al. Among authors: mohamed md. Prog Retin Eye Res. 2016 Jul;53:70-106. doi: 10.1016/j.preteyeres.2016.04.008. Epub 2016 May 10. Prog Retin Eye Res. 2016. PMID: 27173377 Review.
Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinism.
Poulter JA, Al-Araimi M, Conte I, van Genderen MM, Sheridan E, Carr IM, Parry DA, Shires M, Carrella S, Bradbury J, Khan K, Lakeman P, Sergouniotis PI, Webster AR, Moore AT, Pal B, Mohamed MD, Venkataramana A, Ramprasad V, Shetty R, Saktivel M, Kumaramanickavel G, Tan A, Mackey DA, Hewitt AW, Banfi S, Ali M, Inglehearn CF, Toomes C. Poulter JA, et al. Among authors: mohamed md. Am J Hum Genet. 2013 Dec 5;93(6):1143-50. doi: 10.1016/j.ajhg.2013.11.002. Epub 2013 Nov 27. Am J Hum Genet. 2013. PMID: 24290379 Free PMC article. Review.
Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy.
Poulter JA, Ali M, Gilmour DF, Rice A, Kondo H, Hayashi K, Mackey DA, Kearns LS, Ruddle JB, Craig JE, Pierce EA, Downey LM, Mohamed MD, Markham AF, Inglehearn CF, Toomes C. Poulter JA, et al. Among authors: mohamed md. Am J Hum Genet. 2016 Mar 3;98(3):592. doi: 10.1016/j.ajhg.2016.02.017. Epub 2016 Mar 3. Am J Hum Genet. 2016. PMID: 28863275 Free PMC article. No abstract available.
A 5-year-old boy with left flank mass and pain: Questions.
Ag NJ, S NA, Md MA, Cj NA, F T, I MI. Ag NJ, et al. Among authors: md ma. Pediatr Nephrol. 2022 Apr;37(4):797-799. doi: 10.1007/s00467-021-05322-2. Epub 2021 Nov 18. Pediatr Nephrol. 2022. PMID: 34796397 No abstract available.
Clinical Features of a Retinopathy Associated With a Dominant Allele of the RGR Gene.
Ba-Abbad R, Leys M, Wang X, Chakarova C, Waseem N, Carss KJ, Raymond FL, Bujakowska KM, Pierce EA, Mahroo OA, Mohamed MD, Holder GE, Hummel M, Arno G, Webster AR. Ba-Abbad R, et al. Among authors: mohamed md. Invest Ophthalmol Vis Sci. 2018 Oct 1;59(12):4812-4820. doi: 10.1167/iovs.18-25061. Invest Ophthalmol Vis Sci. 2018. PMID: 30347075 Free PMC article.
A 5-year-old boy with left flank mass and pain: Answers.
Ag NJ, S NA, Md MA, Cj NA, F T, I MI. Ag NJ, et al. Among authors: md ma. Pediatr Nephrol. 2022 Apr;37(4):801-803. doi: 10.1007/s00467-021-05323-1. Epub 2021 Nov 18. Pediatr Nephrol. 2022. PMID: 34796396 No abstract available.
Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy.
Poulter JA, Ali M, Gilmour DF, Rice A, Kondo H, Hayashi K, Mackey DA, Kearns LS, Ruddle JB, Craig JE, Pierce EA, Downey LM, Mohamed MD, Markham AF, Inglehearn CF, Toomes C. Poulter JA, et al. Among authors: mohamed md. Am J Hum Genet. 2010 Feb 12;86(2):248-53. doi: 10.1016/j.ajhg.2010.01.012. Am J Hum Genet. 2010. PMID: 20159112 Free PMC article.
42 results