380 related articles for article (PubMed ID: 18700883)
1. Dystrophia Helsinglandica: a new type of hereditary corneal recurrent erosions with late subepithelial fibrosis.
Hammar B; Björck E; Lind H; Lagerstedt K; Dellby A; Fagerholm P
Acta Ophthalmol; 2009 Sep; 87(6):659-65. PubMed ID: 18700883
[TBL] [Abstract][Full Text] [Related]
2. A new corneal disease with recurrent erosive episodes and autosomal-dominant inheritance.
Hammar B; Björck E; Lagerstedt K; Dellby A; Fagerholm P
Acta Ophthalmol; 2008 Nov; 86(7):758-63. PubMed ID: 18778339
[TBL] [Abstract][Full Text] [Related]
3. Dystrophia Helsinglandica--corneal morphology, topography and sensitivity in a hereditary corneal disease with recurrent erosive episodes.
Neira W; Hammar B; Holopainen JM; Tuisku I; Dellby A; Tervo T; Fagerholm P
Acta Ophthalmol; 2010 Jun; 88(4):401-6. PubMed ID: 20597871
[TBL] [Abstract][Full Text] [Related]
4. The TGFBI A546D mutation causes an atypical type of lattice corneal dystrophy.
Correa-Gomez V; Villalvazo-Cordero L; Zenteno JC
Mol Vis; 2007 Sep; 13():1695-700. PubMed ID: 17893671
[TBL] [Abstract][Full Text] [Related]
5. Franceschetti hereditary recurrent corneal erosion.
Lisch W; Bron AJ; Munier FL; Schorderet DF; Tiab L; Lange C; Saikia P; Reinhard T; Weiss JS; Gundlach E; Pleyer U; Lisch C; Auw-Haedrich C
Am J Ophthalmol; 2012 Jun; 153(6):1073-81.e4. PubMed ID: 22402249
[TBL] [Abstract][Full Text] [Related]
6. [Clinical appearance of corneal lattice-type dystrophy (author's transl)].
Lisch W
Klin Monbl Augenheilkd; 1980 Sep; 177(3):284-91. PubMed ID: 7005516
[TBL] [Abstract][Full Text] [Related]
7. A new, X-linked endothelial corneal dystrophy.
Schmid E; Lisch W; Philipp W; Lechner S; Göttinger W; Schlötzer-Schrehardt U; Müller T; Utermann G; Janecke AR
Am J Ophthalmol; 2006 Mar; 141(3):478-487. PubMed ID: 16490493
[TBL] [Abstract][Full Text] [Related]
8. Absence of ocular manifestations in autosomal dominant Alport syndrome associated with haematological abnormalties.
Colville D; Wang YY; Jamieson R; Collins F; Hood J; Savige J
Ophthalmic Genet; 2000 Dec; 21(4):217-25. PubMed ID: 11135492
[TBL] [Abstract][Full Text] [Related]
9. [Mutations in the keratin gene as a cause of Meesman-Wilke corneal dystrophy and autosomal dominant skin cornification disorders].
Swensson O; Swensson B; Nölle B; Rochels R; Wannke B; Thiel HJ
Klin Monbl Augenheilkd; 2000 Jul; 217(1):43-51. PubMed ID: 10949816
[TBL] [Abstract][Full Text] [Related]
10. Dominant optic atrophy. Refining the clinical diagnostic criteria in light of genetic linkage studies.
Johnston RL; Seller MJ; Behnam JT; Burdon MA; Spalton DJ
Ophthalmology; 1999 Jan; 106(1):123-8. PubMed ID: 9917792
[TBL] [Abstract][Full Text] [Related]
11. Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene.
Bredrup C; Knappskog PM; Majewski J; Rødahl E; Boman H
Invest Ophthalmol Vis Sci; 2005 Feb; 46(2):420-6. PubMed ID: 15671264
[TBL] [Abstract][Full Text] [Related]
12. Spontaneous and inheritable R555Q mutation in the TGFBI/BIGH3 gene in two unrelated families exhibiting Bowman's layer corneal dystrophy.
Zhao XC; Nakamura H; Subramanyam S; Stock LE; Gillette TE; Yoshikawa S; Ma X; Yee RW
Ophthalmology; 2007 Nov; 114(11):e39-46. PubMed ID: 17980739
[TBL] [Abstract][Full Text] [Related]
13. A subset of patients with epithelial basement membrane corneal dystrophy have mutations in TGFBI/BIGH3.
Boutboul S; Black GC; Moore JE; Sinton J; Menasche M; Munier FL; Laroche L; Abitbol M; Schorderet DF
Hum Mutat; 2006 Jun; 27(6):553-7. PubMed ID: 16652336
[TBL] [Abstract][Full Text] [Related]
14. A corneal dystrophy associated with transforming growth factor beta-induced Gly623Asp mutation an amyloidogenic phenotype.
Auw-Haedrich C; Agostini H; Clausen I; Reinhard T; Eberwein P; Schorderet DF; Gruenauer-Kloevekorn C
Ophthalmology; 2009 Jan; 116(1):46-51. PubMed ID: 19019446
[TBL] [Abstract][Full Text] [Related]
15. Fleck (Mouchetée) dystrophy of the cornea.
Patten JT; Hyndiuk RA; Donaldson DD; Herman SJ; Ostler HB
Ann Ophthalmol; 1976 Jan; 8(1):25-32. PubMed ID: 1082286
[TBL] [Abstract][Full Text] [Related]
16. A COL17A1 Splice-Altering Mutation Is Prevalent in Inherited Recurrent Corneal Erosions.
Oliver VF; van Bysterveldt KA; Cadzow M; Steger B; Romano V; Markie D; Hewitt AW; Mackey DA; Willoughby CE; Sherwin T; Crosier PS; McGhee CN; Vincent AL
Ophthalmology; 2016 Apr; 123(4):709-22. PubMed ID: 26786512
[TBL] [Abstract][Full Text] [Related]
17. Exclusion of known corneal dystrophy genes in an autosomal dominant pedigree of a unique anterior membrane corneal dystrophy.
Vincent AL; Markie DM; De Karolyi B; Wheeldon CE; Patel DV; Grupcheva CN; McGhee CN
Mol Vis; 2009 Aug; 15():1700-8. PubMed ID: 19710953
[TBL] [Abstract][Full Text] [Related]
18. Dystrophia Smolandiensis: a novel morphological picture of recurrent corneal erosions.
Hammar B; Lagali N; Ek S; Seregard S; Dellby A; Fagerholm P
Acta Ophthalmol; 2010 Jun; 88(4):394-400. PubMed ID: 19681763
[TBL] [Abstract][Full Text] [Related]
19. Epithelial basement membrane dystrophy: evaluation with the HRT II Rostock Cornea Module.
Labbé A; Nicola RD; Dupas B; Auclin F; Baudouin C
Ophthalmology; 2006 Aug; 113(8):1301-8. PubMed ID: 16877069
[TBL] [Abstract][Full Text] [Related]
20. A novel variant lattice corneal dystrophy caused by association of mutation (V625D) in TGFBI gene.
Tian X; Fujiki K; Zhang Y; Murakami A; Li Q; Kanai A; Wang W; Hao Y; Ma Z
Am J Ophthalmol; 2007 Sep; 144(3):473-5. PubMed ID: 17765440
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
