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Journal Abstract Search

288 related items for PubMed ID: 4141632

  • 21. Electron microscopic studies on Fuchs'combined dystrophy. I. Posterior portion of the cornea.
    Iwamoto T, DeVoe AG.
    Invest Ophthalmol; 1971 Jan; 10(1):9-28. PubMed ID: 4099043
    [No Abstract] [Full Text] [Related]

  • 22. Comparison between posterior polymorphous dystrophy and congenital hereditary endothelial dystrophy of the cornea.
    McCartney AC, Kirkness CM.
    Eye (Lond); 1988 Jan; 2 ( Pt 1)():63-70. PubMed ID: 3261696
    [Abstract] [Full Text] [Related]

  • 23. Macular corneal dystrophy-a localized disorder of mucopolysaccharides metabolism?
    Klintworth GK.
    Prog Clin Biol Res; 1982 Jan; 82():69-101. PubMed ID: 6810373
    [No Abstract] [Full Text] [Related]

  • 24. An ultrastructure study of posterior polymorphous dystrophy of the cornea.
    Hanna C, Fraunfelder FT, McNair JR.
    Ann Ophthalmol; 1977 Nov; 9(11):1371-8. PubMed ID: 303882
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  • 28. [The ultrastructive of spotty corneal dystrophy (Groenouw II) (author's transl)].
    Hanselmayer H, Roll P.
    Klin Monbl Augenheilkd; 1975 Nov; 167(5):690-7. PubMed ID: 128655
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  • 30. Light microscopical and polarisation optical study of the lattice dystrophy of the cornea.
    François J, Fehér J.
    Ophthalmologica; 1972 Nov; 164(1):1-18. PubMed ID: 4536878
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  • 33. Synchrotron X-ray diffraction in atypical macular dystrophy.
    Quantock AJ, Meek KM, Thonar EJ, Assil KK.
    Eye (Lond); 1993 Nov; 7 ( Pt 6)():779-84. PubMed ID: 8119433
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  • 35. Macular corneal dystrophy.
    Ghosh M, McCulloch C.
    Can J Ophthalmol; 1973 Oct; 8(4):515-26. PubMed ID: 4127427
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  • 36. On the role of kerato-epithelin in the pathogenesis of 5q31-linked corneal dystrophies.
    Korvatska E, Munier FL, Chaubert P, Wang MX, Mashima Y, Yamada M, Uffer S, Zografos L, Schorderet DF.
    Invest Ophthalmol Vis Sci; 1999 Sep; 40(10):2213-9. PubMed ID: 10476785
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  • 37. [Polymorphic posterior corneal dystrophy. Histological and ultrastructural study of 2 cases].
    Renard G, Petroutsos G, Savoldelli M, Pouliquen Y.
    J Fr Ophtalmol; 1983 Sep; 6(1):7-23. PubMed ID: 6601674
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  • 38. 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
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  • 39. Lattice corneal dystrophy type III with corneal fistula. A case report.
    Sridhar MS, Sridhar U, Vemuganti GK, Mandal AK.
    Indian J Ophthalmol; 2004 Sep; 52(3):236-8. PubMed ID: 15510466
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