Similar articles for PMID: 25138764

Year	Number of Results
1988	1
1998	2
1999	1
2001	1
2003	1
2005	1
2006	7
2007	8
2008	3
2009	3
2010	8
2011	2
2012	3
2013	11
2014	10
2015	8
2016	8
2017	4
2018	5
2019	5
2020	4
2021	6
2022	2
2024	0

1

Two novel mutations including a large deletion of the SLC4A11 gene causing autosomal recessive hereditary endothelial dystrophy.

Puangsricharern V, Yeetong P, Charumalai C, Suphapeetiporn K, Shotelersuk V. Puangsricharern V, et al. Br J Ophthalmol. 2014 Oct;98(10):1460-2. doi: 10.1136/bjophthalmol-2014-305584. Epub 2014 Aug 19. Br J Ophthalmol. 2014. PMID: 25138764 No abstract available.

2

A novel nonsense mutation of the SLC4A11 gene in a Korean patient with autosomal recessive congenital hereditary endothelial dystrophy.

Park SH, Jeong HJ, Kim M, Kim MS. Park SH, et al. Cornea. 2013 Jul;32(7):e181-2. doi: 10.1097/ICO.0b013e31828d9ffd. Cornea. 2013. PMID: 23615275 No abstract available.

3

Fuchs Endothelial Corneal Dystrophy in a Heterozygous Carrier of Congenital Hereditary Endothelial Dystrophy Type 2 with a Novel Mutation in SLC4A11.

Kim JH, Ko JM, Tchah H. Kim JH, et al. Ophthalmic Genet. 2015;36(3):284-6. doi: 10.3109/13816810.2014.881510. Ophthalmic Genet. 2015. PMID: 24502824

4

Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).

Vithana EN, Morgan P, Sundaresan P, Ebenezer ND, Tan DT, Mohamed MD, Anand S, Khine KO, Venkataraman D, Yong VH, Salto-Tellez M, Venkatraman A, Guo K, Hemadevi B, Srinivasan M, Prajna V, Khine M, Casey JR, Inglehearn CF, Aung T. Vithana EN, et al. Nat Genet. 2006 Jul;38(7):755-7. doi: 10.1038/ng1824. Epub 2006 Jun 11. Nat Genet. 2006. PMID: 16767101

5

Coexistence of Congenital Hereditary Endothelial Dystrophy and Fuchs Endothelial Corneal Dystrophy Associated With SLC4A11 Mutations in Affected Families.

Chaurasia S, Ramappa M, Annapurna M, Kannabiran C. Chaurasia S, et al. Cornea. 2020 Mar;39(3):354-357. doi: 10.1097/ICO.0000000000002183. Cornea. 2020. PMID: 31714402

6

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

7

Molecular phenotype of SLC4A11 missense mutants: Setting the stage for personalized medicine in corneal dystrophies.

Alka K, Casey JR. Alka K, et al. Hum Mutat. 2018 May;39(5):676-690. doi: 10.1002/humu.23401. Epub 2018 Feb 2. Hum Mutat. 2018. PMID: 29327391

8

Mutations in the Corneal Endothelial Dystrophy-Associated Gene SLC4A11 Render the Cells More Vulnerable to Oxidative Insults.

Roy S, Praneetha DC, Vendra VP. Roy S, et al. Cornea. 2015 Jun;34(6):668-74. doi: 10.1097/ICO.0000000000000421. Cornea. 2015. PMID: 25811729

9

Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused by SLC4A11 mutations.

Vilas GL, Loganathan SK, Quon A, Sundaresan P, Vithana EN, Casey J. Vilas GL, et al. Hum Mutat. 2012 Feb;33(2):419-28. doi: 10.1002/humu.21655. Epub 2011 Dec 20. Hum Mutat. 2012. PMID: 22072594

10

Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophy.

Hemadevi B, Veitia RA, Srinivasan M, Arunkumar J, Prajna NV, Lesaffre C, Sundaresan P. Hemadevi B, et al. Arch Ophthalmol. 2008 May;126(5):700-8. doi: 10.1001/archopht.126.5.700. Arch Ophthalmol. 2008. PMID: 18474783

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