These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
48. In vivo laser confocal microscopy findings for Bowman's layer dystrophies (Thiel-Behnke and Reis-Bücklers corneal dystrophies). Kobayashi A; Sugiyama K Ophthalmology; 2007 Jan; 114(1):69-75. PubMed ID: 17198850 [TBL] [Abstract][Full Text] [Related]
49. Genetics of corneal dystrophies: the evolving landscape. Pieramici SF; Afshari NA Curr Opin Ophthalmol; 2006 Aug; 17(4):361-6. PubMed ID: 16900028 [TBL] [Abstract][Full Text] [Related]
50. Clinical, histologic, and ultrastructural features of the corneal dystrophy caused by the R124L mutation of the BIGH3 gene. Dighiero P; Valleix S; D'Hermies F; Drunat S; Ellies P; Savoldelli M; Pouliquen Y; Delpech M; Legeais JM; Renard G Ophthalmology; 2000 Jul; 107(7):1353-7. PubMed ID: 10889112 [TBL] [Abstract][Full Text] [Related]
51. 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]
52. Association of autosomal dominantly inherited corneal dystrophies with BIGH3 gene mutations in Japan. Mashima Y; Yamamoto S; Inoue Y; Yamada M; Konishi M; Watanabe H; Maeda N; Shimomura Y; Kinoshita S Am J Ophthalmol; 2000 Oct; 130(4):516-7. PubMed ID: 11024425 [TBL] [Abstract][Full Text] [Related]
54. Lattice corneal dystrophy type I without typical lattice lines: role of mutational analysis. Yoshida S; Yoshida A; Nakao S; Emori A; Nakamura T; Fujisawa K; Kumano Y; Ishibashi T Am J Ophthalmol; 2004 Mar; 137(3):586-8. PubMed ID: 15013897 [TBL] [Abstract][Full Text] [Related]
55. The morphogenesis of granular and lattice corneal dystrophy - A mutation combination hypothesis. Sabir M Med Hypotheses; 2020 Dec; 145():110291. PubMed ID: 33039949 [TBL] [Abstract][Full Text] [Related]
56. Investigation of TGFBI (transforming growth factor beta-induced) Gene Mutations in Families with Granular Corneal Dystrophy Type 1 in the Konya Region. Malkondu F; Arıkoğlu H; Erkoç Kaya D; Bozkurt B; Özkan F Turk J Ophthalmol; 2020 Apr; 50(2):64-70. PubMed ID: 32366062 [TBL] [Abstract][Full Text] [Related]
57. Phenotype associated with the H626P mutation and other changes in the TGFBI gene in Czech families. Liskova P; Klintworth GK; Bowling BL; Filipec M; Jirsova K; Tuft SJ; Bhattacharya SS; Hardcastle AJ; Ebenezer ND Ophthalmic Res; 2008; 40(2):105-8. PubMed ID: 18259096 [TBL] [Abstract][Full Text] [Related]