199 related articles for article (PubMed ID: 34003075)
1. Corneal ectasia associated with posterior lamellar opacification.
Yung M; Chen AC; Chung DD; Barrington A; Zhang J; Frausto RF; Magalhaes OA; Aldave AJ
Ophthalmic Genet; 2021 Aug; 42(4):486-492. PubMed ID: 34003075
[TBL] [Abstract][Full Text] [Related]
2. Confirmation and refinement of the heterozygous deletion of the small leucine-rich proteoglycans associated with posterior amorphous corneal dystrophy.
Cervantes AE; Gee KM; Whiting MF; Frausto RF; Aldave AJ
Ophthalmic Genet; 2018 Aug; 39(4):419-424. PubMed ID: 29671669
[TBL] [Abstract][Full Text] [Related]
3. Posterior Amorphous Corneal Dystrophy Associated With Keratoglobus: A Case Report.
Fay J; Herzlich AA; Florakis GJ
Cornea; 2017 Dec; 36(12):1562-1566. PubMed ID: 28902010
[TBL] [Abstract][Full Text] [Related]
4. Classification of posterior polymorphous corneal dystrophy as a corneal ectatic disorder following confirmation of associated significant corneal steepening.
Aldave AJ; Ann LB; Frausto RF; Nguyen CK; Yu F; Raber IM
JAMA Ophthalmol; 2013 Dec; 131(12):1583-90. PubMed ID: 24113819
[TBL] [Abstract][Full Text] [Related]
5. Ophthalmic findings in patients with arterial tortuosity syndrome and carriers: A case series.
Hardin JS; Zarate YA; Callewaert B; Phillips PH; Warner DB
Ophthalmic Genet; 2018; 39(1):29-34. PubMed ID: 28726533
[TBL] [Abstract][Full Text] [Related]
6. Bilateral central anterior stromal opacity of the cornea: dystrophy or degeneration?
Toker E; Bavbek T
Eur J Ophthalmol; 2003 Apr; 13(3):315-9. PubMed ID: 12747655
[TBL] [Abstract][Full Text] [Related]
7. Posterior Amorphous Corneal Dystrophy: New Chromosomal Breakpoints in the Small Leucine-Rich Proteoglycan-Coding Region.
Basbus FJ; Cremona FA; Lucero Saá F; Chiaradía PA; Francipane L; Menazzi S
Cornea; 2022 Apr; 41(4):491-495. PubMed ID: 35044970
[TBL] [Abstract][Full Text] [Related]
8. A novel homozygous ZNF469 variant causing brittle cornea syndrome is associated with corneal ectasias in heterozygous carriers.
Arce-González R; Chacon-Camacho OF; Ordoñez-Labastida V; Graue-Hernandez EO; Navas-Pérez A; Zenteno JC
Int Ophthalmol; 2023 Mar; 43(3):807-815. PubMed ID: 36048286
[TBL] [Abstract][Full Text] [Related]
9. Thick keratoconic cornea associated with posterior polymorphous corneal dystrophy.
Zaarour K; Slim E; Antoun J; Waked N
J Fr Ophtalmol; 2017 Mar; 40(3):232-236. PubMed ID: 28089285
[TBL] [Abstract][Full Text] [Related]
10. Posterior amorphous corneal dystrophy caused by a de novo deletion.
Odent S; Casteels I; Cassiman C; Dieltiëns M; Hua MT; Devriendt K
Ophthalmic Genet; 2017; 38(2):167-170. PubMed ID: 27096414
[TBL] [Abstract][Full Text] [Related]
11. Bilateral Atypical Granular Corneal Dystrophy Associated with Unilateral Keratoconus in a Male Child.
Dangra KL; Das M; Periasamy S; Prajna NV
Middle East Afr J Ophthalmol; 2016; 23(3):262-4. PubMed ID: 27555713
[TBL] [Abstract][Full Text] [Related]
12. Unusual presentation of presumed posterior polymorphous dystrophy associated with iris heterochromia, band keratopathy, and keratoconus.
Lam HY; Wiggs JL; Jurkunas UV
Cornea; 2010 Oct; 29(10):1180-5. PubMed ID: 20567203
[TBL] [Abstract][Full Text] [Related]
13. Identification of Mutations in the PRDM5 Gene in Brittle Cornea Syndrome.
Micheal S; Khan MI; Islam F; Akhtar F; Qamar R; Tassignon MJ; Loeys B; den Hollander AI
Cornea; 2016 Jun; 35(6):853-9. PubMed ID: 27032025
[TBL] [Abstract][Full Text] [Related]
14. Keratoglobus in association with posterior polymorphous dystrophy.
Harissi-Dagher M; Dana MR; Jurkunas UV
Cornea; 2007 Dec; 26(10):1288-91. PubMed ID: 18043197
[TBL] [Abstract][Full Text] [Related]
15. Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation.
Lechner J; Dash DP; Muszynska D; Hosseini M; Segev F; George S; Frazer DG; Moore JE; Kaye SB; Young T; Simpson DA; Churchill AJ; Héon E; Willoughby CE
Invest Ophthalmol Vis Sci; 2013 May; 54(5):3215-23. PubMed ID: 23599324
[TBL] [Abstract][Full Text] [Related]
16. Concurrent macular corneal dystrophy and keratoconus.
Mohammad-Rabei H; Shojaei A; Aslani M
Middle East Afr J Ophthalmol; 2012; 19(2):251-3. PubMed ID: 22623870
[TBL] [Abstract][Full Text] [Related]
17. Posterior amorphous corneal dystrophy in a patient with 12q21.33 deletion.
Lenk J; Porrmann J; Smitka M; Eger I; Schröck E; Hackmann K; Herber R; Raiskup F; Tzschach A
Ophthalmic Genet; 2018 Oct; 39(5):645-647. PubMed ID: 30058938
[TBL] [Abstract][Full Text] [Related]
18. Bruch's membrane abnormalities in PRDM5-related brittle cornea syndrome.
Porter LF; Gallego-Pinazo R; Keeling CL; Kamieniorz M; Zoppi N; Colombi M; Giunta C; Bonshek R; Manson FD; Black GC
Orphanet J Rare Dis; 2015 Nov; 10():145. PubMed ID: 26560304
[TBL] [Abstract][Full Text] [Related]
19. Vortex Pattern of Corneal Deposits in Granular Corneal Dystrophy Associated With the p.(Arg555Trp) Mutation in TGFBI.
Kattan JM; Serna-Ojeda JC; Sharma A; Kim EK; Ramirez-Miranda A; Cruz-Aguilar M; Cervantes AE; Frausto RF; Zenteno JC; Graue-Hernandez EO; Aldave AJ
Cornea; 2017 Feb; 36(2):210-216. PubMed ID: 28060069
[TBL] [Abstract][Full Text] [Related]
20. A novel characterization of posterior keratoconus using anterior segment optical coherence tomography in an infant: a case report.
Garg N; Chang TC; Reiser BJ; Cavuoto KM
BMC Ophthalmol; 2015 Nov; 15():158. PubMed ID: 26537455
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]