Similar articles for PMID: 36613650

Year	Number of Results
1980	1
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1997	1
1999	1
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1

Posterior Polymorphous Corneal Dystrophy in a Patient with a Novel ZEB1 Gene Mutation.

Fernández-Gutiérrez E, Fernández-Pérez P, Boto-De-Los-Bueis A, García-Fernández L, Rodríguez-Solana P, Solís M, Vallespín E. Fernández-Gutiérrez E, et al. Int J Mol Sci. 2022 Dec 22;24(1):209. doi: 10.3390/ijms24010209. Int J Mol Sci. 2022. PMID: 36613650 Free PMC article.

2

Posterior Polymorphous Corneal Dystrophy: Clinical-Pathologic Correlation.

Safran JP, Hammersmith KM, Milman T. Safran JP, et al. Ophthalmology. 2023 Dec;130(12):1354. doi: 10.1016/j.ophtha.2023.03.003. Epub 2023 Apr 12. Ophthalmology. 2023. PMID: 37055288 No abstract available.

3

Unilateral posterior polymorphous corneal dystrophy due to a novel ZEB1 gene mutation in a Korean girl.

Lee CY, Jang JH, Han G, Chung TY, Lim DH. Lee CY, et al. Ophthalmic Genet. 2022 Oct;43(5):724-728. doi: 10.1080/13816810.2022.2106495. Epub 2022 Aug 31. Ophthalmic Genet. 2022. PMID: 36043701 No abstract available.

4

Descemet Membrane Endothelial Keratoplasty (DMEK) for Severe Verrucous Posterior Polymorphous Corneal Dystrophy with Uncommon Clinical and Ultrastructural Findings.

Berger T, Seitz B, Löw U, Flockerzi F, Schlötzer-Schrehardt U, Daas L. Berger T, et al. Klin Monbl Augenheilkd. 2022 Aug 4. doi: 10.1055/a-1862-8403. Online ahead of print. Klin Monbl Augenheilkd. 2022. PMID: 35926514 English.

5

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.

6

Posterior corneal vesicles are not associated with the genetic variants that cause posterior polymorphous corneal dystrophy.

Liskova P, Hafford-Tear NJ, Skalicka P, Malinka F, Jedlickova J, Ďuďáková Ľ, Pontikos N, Davidson AE, Tuft S. Liskova P, et al. Acta Ophthalmol. 2022 Nov;100(7):e1426-e1430. doi: 10.1111/aos.15114. Epub 2022 Feb 17. Acta Ophthalmol. 2022. PMID: 35174971 Free article.

7

[Imaging features of posterior polymorphous corneal dystrophy observed by in vivo confocal microscopy].

Gu SF, Peng RM, Xiao GG, Hong J. Gu SF, et al. Zhonghua Yan Ke Za Zhi. 2022 Feb 11;58(2):103-111. doi: 10.3760/cma.j.cn112142-20210228-00099. Zhonghua Yan Ke Za Zhi. 2022. PMID: 35144350 Chinese.

8

c.-61G>A in OVOL2 is a Pathogenic 5' Untranslated Region Variant Causing Posterior Polymorphous Corneal Dystrophy 1.

Janeschitz-Kriegl L, Kamdar D, Quinodoz M, Kaminska K, Folcher M, György B, Meyer P, Wild A, Escher P, Scholl HPN, Rivolta C, Goldblum D. Janeschitz-Kriegl L, et al. Cornea. 2022 Jan 1;41(1):89-94. doi: 10.1097/ICO.0000000000002843. Cornea. 2022. PMID: 34469340

9

Corneal ectasia associated with posterior lamellar opacification.

Yung M, Chen AC, Chung DD, Barrington A, Zhang J, Frausto RF, Magalhaes OA, Aldave AJ. Yung M, et al. Ophthalmic Genet. 2021 Aug;42(4):486-492. doi: 10.1080/13816810.2021.1923034. Epub 2021 May 18. Ophthalmic Genet. 2021. PMID: 34003075

10

Non-Penetrance for Ocular Phenotype in Two Individuals Carrying Heterozygous Loss-of-Function ZEB1 Alleles.

Dudakova L, Stranecky V, Piherova L, Palecek T, Pontikos N, Kmoch S, Skalicka P, Vaneckova M, Davidson AE, Liskova P. Dudakova L, et al. Genes (Basel). 2021 Apr 30;12(5):677. doi: 10.3390/genes12050677. Genes (Basel). 2021. PMID: 33946386 Free PMC article.

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