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4. [Mutational analysis of VSX-1 in one patient with posterior polymorphous corneal dystrophy and in three families with hereditary Fuchs endothelial dystrophy]. Clausen I; Weidle E; Duncker G; Grünauer-Kloevekorn C Klin Monbl Augenheilkd; 2009 Jun; 226(6):466-9. PubMed ID: 19507099 [TBL] [Abstract][Full Text] [Related]
5. Hereditary Fuchs' dystrophy. Sidrys LA Am J Ophthalmol; 1981 Feb; 91(2):277-8. PubMed ID: 6970524 [No Abstract] [Full Text] [Related]
6. 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 Cornea; 2020 Mar; 39(3):354-357. PubMed ID: 31714402 [TBL] [Abstract][Full Text] [Related]
7. Keratoconus and Fuchs' corneal endothelial dystrophy in a patient and her family. Lipman RM; Rubenstein JB; Torczynski E Arch Ophthalmol; 1990 Jul; 108(7):993-4. PubMed ID: 2369360 [TBL] [Abstract][Full Text] [Related]
8. A specular microscopic study of families with endothelial dystrophy. Schnitzer JI; Krachmer JH Br J Ophthalmol; 1981 Jun; 65(6):396-400. PubMed ID: 6973355 [TBL] [Abstract][Full Text] [Related]
9. Parents of Patients With Congenital Hereditary Endothelial Dystrophy Should Be Evaluated for Fuchs Endothelial Corneal Dystrophy. Chaurasia S; Ramappa M; Kannabiran C Cornea; 2017 Dec; 36(12):e34-e35. PubMed ID: 28976417 [No Abstract] [Full Text] [Related]
11. Exclusion of COL8A1, the gene encoding the alpha2(VIII) chain of type VIII collagen, as a candidate for Fuchs endothelial dystrophy and posterior polymorphous corneal dystrophy. Urquhart JE; Biswas S; Black GC; Munier FL; Sutphin J Br J Ophthalmol; 2006 Nov; 90(11):1430-1. PubMed ID: 17057173 [No Abstract] [Full Text] [Related]
12. 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]
13. 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 Ophthalmic Genet; 2015; 36(3):284-6. PubMed ID: 24502824 [TBL] [Abstract][Full Text] [Related]
14. 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 Hum Mol Genet; 2001 Oct; 10(21):2415-23. PubMed ID: 11689488 [TBL] [Abstract][Full Text] [Related]
16. Fuchs' Endothelial Corneal Dystrophy in Patients With Myotonic Dystrophy, Type 1. Winkler NS; Milone M; Martinez-Thompson JM; Raja H; Aleff RA; Patel SV; Fautsch MP; Wieben ED; Baratz KH Invest Ophthalmol Vis Sci; 2018 Jun; 59(7):3053-3057. PubMed ID: 30025114 [TBL] [Abstract][Full Text] [Related]
17. 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 Nat Genet; 2006 Jul; 38(7):755-7. PubMed ID: 16767101 [TBL] [Abstract][Full Text] [Related]
18. The human cornea has a high incidence of acquired chromosome abnormalities. Pettenati MJ; Sweatt AJ; Lantz P; Stanton CA; Reynolds J; Rao PN; Davis RM Hum Genet; 1997 Nov; 101(1):26-9. PubMed ID: 9385364 [TBL] [Abstract][Full Text] [Related]
19. Laser in situ keratomileusis in patients with corneal guttata and family history of Fuchs' endothelial dystrophy. Moshirfar M; Feiz V; Feilmeier MR; Kang PC J Cataract Refract Surg; 2005 Dec; 31(12):2281-6. PubMed ID: 16473218 [TBL] [Abstract][Full Text] [Related]
20. Instability of TCF4 Triplet Repeat Expansion With Parent-Child Transmission in Fuchs' Endothelial Corneal Dystrophy. Saade JS; Xing C; Gong X; Zhou Z; Mootha VV Invest Ophthalmol Vis Sci; 2018 Aug; 59(10):4065-4070. PubMed ID: 30098193 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]