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.
27. A novel UBIAD1 mutation identified in a Chinese family with Schnyder crystalline corneal dystrophy. Jing Y; Liu C; Xu J; Wang L Mol Vis; 2009 Jul; 15():1463-9. PubMed ID: 19649163 [TBL] [Abstract][Full Text] [Related]
28. Genotype-phenotype analysis of Bietti crystalline dystrophy in a family with the CYP4V2 Ile111Thr mutation. García-García GP; López-Garrido MP; Martínez-Rubio M; Moya-Moya MA; Belmonte-Martínez J; Escribano J Cornea; 2013 Jul; 32(7):1002-8. PubMed ID: 23538635 [TBL] [Abstract][Full Text] [Related]
29. Disappearance of crystals in Schnyder's crystalline corneal dystrophy after epithelial erosion. Chern KC; Meisler DM Am J Ophthalmol; 1995 Dec; 120(6):802-3. PubMed ID: 8540558 [TBL] [Abstract][Full Text] [Related]
30. Affected asymptomatic relatives in congenital hereditary endothelial dystrophy. Levenson JE; Chandler JW; Kaufman HE Am J Ophthalmol; 1973 Dec; 76(6):967-71. PubMed ID: 4543367 [No Abstract] [Full Text] [Related]
31. [The different opacity patterns of Lisch corneal dystrophy]. Butros S; Lang GK; Alvarez de Toledo J; Teimann U; Rohrbach JM; Lisch W Klin Monbl Augenheilkd; 2006 Oct; 223(10):837-40. PubMed ID: 17063428 [TBL] [Abstract][Full Text] [Related]
32. Schnyder corneal dystrophy and associated phenotypes caused by novel and recurrent mutations in the UBIAD1 gene. Evans CJ; Dudakova L; Skalicka P; Mahelkova G; Horinek A; Hardcastle AJ; Tuft SJ; Liskova P BMC Ophthalmol; 2018 Sep; 18(1):250. PubMed ID: 30223810 [TBL] [Abstract][Full Text] [Related]
33. Polymorphic amyloid degeneration of the cornea. A clinical and histopathologic study. Mannis MJ; Krachmer JH; Rodrigues MM; Pardos GJ Arch Ophthalmol; 1981 Jul; 99(7):1217-23. PubMed ID: 6973332 [TBL] [Abstract][Full Text] [Related]