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

Year Number of Results
1978 2
1995 2
1999 2
2001 1
2003 2
2004 2
2005 4
2006 4
2007 8
2008 5
2009 5
2010 5
2011 3
2012 4
2013 10
2014 9
2015 9
2016 8
2017 7
2018 6
2019 8
2020 6
2021 16
2022 20
2023 4
2024 1

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Similar articles for PMID: 23662738

134 results

Results by year

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Page 1
Update on the genetics of corneal endothelial dystrophies.
Kannabiran C, Chaurasia S, Ramappa M, Mootha VV. Kannabiran C, et al. Indian J Ophthalmol. 2022 Jul;70(7):2239-2248. doi: 10.4103/ijo.IJO_992_22. Indian J Ophthalmol. 2022. PMID: 35791103 Free PMC article. Review.
Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy.
Biswas S, Munier FL, Yardley J, Hart-Holden N, Perveen R, Cousin P, Sutphin JE, Noble B, Batterbury M, Kielty C, Hackett A, Bonshek R, Ridgway A, McLeod D, Sheffield VC, Stone EM, Schorderet DF, Black GC. Biswas S, et al. Hum Mol Genet. 2001 Oct 1;10(21):2415-23. doi: 10.1093/hmg/10.21.2415. Hum Mol Genet. 2001. PMID: 11689488
SLC4A11 mutations in Fuchs endothelial corneal dystrophy.
Vithana EN, Morgan PE, Ramprasad V, Tan DT, Yong VH, Venkataraman D, Venkatraman A, Yam GH, Nagasamy S, Law RW, Rajagopal R, Pang CP, Kumaramanickevel G, Casey JR, Aung T. Vithana EN, et al. Hum Mol Genet. 2008 Mar 1;17(5):656-66. doi: 10.1093/hmg/ddm337. Epub 2007 Nov 16. Hum Mol Genet. 2008. PMID: 18024964
Observation of nine previously reported and 10 non-reported SLC4A11 mutations among 20 Iranian CHED probands and identification of an MPDZ mutation as possible cause of CHED and FECD in one family.
Moazzeni H, Javadi MA, Asgari D, Khani M, Emami M, Moghadam A, Panahi-Bazaz MR, Hosseini Tehrani M, Karimian F, Hosseini B, Nekuie Moghadam T, Hassanpour H, Akbari MT, Elahi E. Moazzeni H, et al. Br J Ophthalmol. 2020 Nov;104(11):1621-1628. doi: 10.1136/bjophthalmol-2019-314377. Epub 2019 Aug 16. Br J Ophthalmol. 2020. PMID: 31420327
134 results