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29. Light microscopical and polarisation optical study of the macular dystrophy of the cornea. François J; Fehér J Ophthalmologica; 1972; 164(1):19-34. PubMed ID: 4259206 [No Abstract] [Full Text] [Related]
30. Novel gene mutation in a patient with Bietti crystalline dystrophy without corneal deposits. Raoof N; Vincent AL Clin Exp Ophthalmol; 2017 May; 45(4):421-424. PubMed ID: 28097764 [No Abstract] [Full Text] [Related]
31. [Dystrophies of the cornea in children]. Pouliquen V; Saragoussi JJ Annee Ther Clin Ophtalmol; 1983; 34():209-22. PubMed ID: 6333205 [No Abstract] [Full Text] [Related]
32. A possibly new familial superficial corneal dystrophy. Smith EL; Wilson WM; Williams DK Can J Ophthalmol; 1971 Jan; 6(1):30-7. PubMed ID: 5313312 [No Abstract] [Full Text] [Related]
34. Genome sequencing identifies a non-coding variant in the MCDR1 locus as a cause of macular dystrophy. Ellingford JM; Sergouniotis PI; Jenkins E; Black GC Clin Exp Ophthalmol; 2017 Apr; 45(3):297-299. PubMed ID: 27551809 [No Abstract] [Full Text] [Related]
36. Macular dystrophy of the cornea. Ultrastructure of two cases. Tremblay M; Dubé I Can J Ophthalmol; 1973 Jan; 8(1):47-53. PubMed ID: 4122333 [No Abstract] [Full Text] [Related]
37. [Histological and electron microscopic studies on Meesmann-Wilke's hereditary dystrophy of the corneal epithelium]. Thiel HJ Ber Zusammenkunft Dtsch Ophthalmol Ges; 1968; 68():213-5. PubMed ID: 5306062 [No Abstract] [Full Text] [Related]
38. Corneal dystrophies and genetics in the International Committee for Classification of Corneal Dystrophies era: a review. Vincent AL Clin Exp Ophthalmol; 2014; 42(1):4-12. PubMed ID: 24433354 [TBL] [Abstract][Full Text] [Related]
39. [Macular corneal dystrophy--differential diagnosis and genetics of a far-advanced case]. Stolze HH; Goerdt J; Reim M Fortschr Ophthalmol; 1987; 84(3):239-41. PubMed ID: 3497856 [No Abstract] [Full Text] [Related]
40. Assessment of incorporation of the International Committee for Classification of Corneal Dystrophies (IC3D) in literature. AlRyalat SA; Jaber BA Ophthalmic Genet; 2020 Oct; 41(5):507-509. PubMed ID: 32856495 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]