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.


PUBMED FOR HANDHELDS

Journal Abstract Search


142 related items for PubMed ID: 4543367

  • 1. 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]

  • 2. Electron microscopic study of hereditary corneal edema.
    Kanai A, Waltman S, Polack FM, Kaufman HE.
    Invest Ophthalmol; 1971 Feb; 10(2):89-99. PubMed ID: 4925768
    [No Abstract] [Full Text] [Related]

  • 3. Macular corneal dystrophy.
    Ghosh M, McCulloch C.
    Can J Ophthalmol; 1973 Oct; 8(4):515-26. PubMed ID: 4127427
    [No Abstract] [Full Text] [Related]

  • 4. Lattice dystrophy type 1: a report of 8 families.
    Tsubota K, Hida T, Murata H, Akiya S, Shinji T, Kimura W.
    Ophthalmologica; 1987 Oct; 194(2-3):71-6. PubMed ID: 3497371
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Congenital hereditary stromal dystrophy of the cornea.
    Witschel H, Fine BS, Grützner P, McTigue JW.
    Arch Ophthalmol; 1978 Jun; 96(6):1043-51. PubMed ID: 350201
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Congenital endothelial corneal dystrophy. Clinical, pathological, and genetic study.
    Pearce WG, Tripathi RC, Morgan G.
    Br J Ophthalmol; 1969 Sep; 53(9):577-91. PubMed ID: 4900143
    [No Abstract] [Full Text] [Related]

  • 9. New findings in posterior amorphous corneal dystrophy.
    Dunn SP, Krachmer JH, Ching SS.
    Arch Ophthalmol; 1984 Feb; 102(2):236-9. PubMed ID: 6607727
    [Abstract] [Full Text] [Related]

  • 10. The histological and ultrastructural pathology of congenital hereditary corneal dystrophy: a case report.
    Kenyon KR, Maumenee AE.
    Invest Ophthalmol; 1968 Oct; 7(5):475-500. PubMed ID: 4234642
    [No Abstract] [Full Text] [Related]

  • 11. The honeycomb type of Reis-Bücklers' dystrophy of the cornea: biometrics and an interpretation.
    Wittebol-Post D, van Bijsterveld OP, Delleman JW.
    Ophthalmologica; 1987 Oct; 194(2-3):65-70. PubMed ID: 3497370
    [Abstract] [Full Text] [Related]

  • 12. [Histopathology of Schlichting's posterior polymorphous corneal dystrophy. I. Light microscopy findings in relation to clinical aspects].
    Hanselmayer H.
    Albrecht Von Graefes Arch Klin Exp Ophthalmol; 1972 Oct; 184(4):345-57. PubMed ID: 4537983
    [No Abstract] [Full Text] [Related]

  • 13. The nature of hereditary deep polymorphous dystrophy of the cornea: its association with iris and anterior chamber dygenesis.
    Grayson M.
    Trans Am Ophthalmol Soc; 1974 Oct; 72():516-59. PubMed ID: 4549335
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. The pathogenesis of congenital hereditary endothelial dystrophy of the cornea.
    Kenyon KR, Antine B.
    Am J Ophthalmol; 1971 Oct; 72(4):787-95. PubMed ID: 5315521
    [No Abstract] [Full Text] [Related]

  • 16. Further studies of congenital hereditary endothelial dystrophy of the cornea.
    Kenyon KR, Maumenee AE.
    Am J Ophthalmol; 1973 Oct; 76(4):419-39. PubMed ID: 4270338
    [No Abstract] [Full Text] [Related]

  • 17. Posterior amorphous corneal dystrophy. An ultrastructural study of a variant with histopathological features of an endothelial dystrophy.
    Roth SI, Mittelman D, Stock EL.
    Cornea; 1992 Mar; 11(2):165-72. PubMed ID: 1582220
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. [Familial congenital dystrophy of the corneal stroma: Turpin's syndrome (author's transl)].
    Pouliquen Y, Lacombe E, Schreinzer C, Giraud JP, Savoldelli M.
    J Fr Ophtalmol; 1979 Feb; 2(2):115-25. PubMed ID: 312637
    [Abstract] [Full Text] [Related]

  • 20. Mesenchymal dysgenesis in Peter's anomaly, sclerocornea and congenital endothelial dystrophy.
    Kenyon KR.
    Exp Eye Res; 1975 Aug; 21(2):125-42. PubMed ID: 1100415
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 8.