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Journal Abstract Search

147 related items for PubMed ID: 3872072

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. [Heredofamilial corneal dystrophies].
    François J.
    Ber Zusammenkunft Dtsch Ophthalmol Ges; 1972; 71():171-222. PubMed ID: 4126168
    [No Abstract] [Full Text] [Related]

  • 23.
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  • 24. Hereditary lattice corneal dystrophy is associated with corneal amyloid deposits enclosing C-terminal fragments of keratoepithelin.
    Stix B, Leber M, Bingemer P, Gross C, Rüschoff J, Fändrich M, Schorderet DF, Vorwerk CK, Zacharias M, Roessner A, Röcken C.
    Invest Ophthalmol Vis Sci; 2005 Apr; 46(4):1133-9. PubMed ID: 15790870
    [Abstract] [Full Text] [Related]

  • 25. [The course of spinocerebellar degeneration (clinico-morphologic correlation)].
    Musatova IV, Chaikovskaia RP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1974 Apr; 74(12):1788-93. PubMed ID: 4450908
    [No Abstract] [Full Text] [Related]

  • 26. [Polymorphic posterior corneal dystrophy. Histological and ultrastructural study of 2 cases].
    Renard G, Petroutsos G, Savoldelli M, Pouliquen Y.
    J Fr Ophtalmol; 1983 Apr; 6(1):7-23. PubMed ID: 6601674
    [Abstract] [Full Text] [Related]

  • 27. Recurrence of corneal dystrophy after excimer laser phototherapeutic keratectomy.
    Dinh R, Rapuano CJ, Cohen EJ, Laibson PR.
    Ophthalmology; 1999 Aug; 106(8):1490-7. PubMed ID: 10442892
    [Abstract] [Full Text] [Related]

  • 28. Lattice corneal dystrophy type II with familial amyloid polyneuropathy type IV.
    Asaoka T, Amano S, Sunada Y, Sawa M.
    Jpn J Ophthalmol; 1993 Aug; 37(4):426-31. PubMed ID: 8145387
    [Abstract] [Full Text] [Related]

  • 29. Keratoconus associated with other corneal dystrophies.
    Cremona FA, Ghosheh FR, Rapuano CJ, Eagle RC, Hammersmith KM, Laibson PR, Ayres BD, Cohen EJ.
    Cornea; 2009 Feb; 28(2):127-35. PubMed ID: 19158551
    [Abstract] [Full Text] [Related]

  • 30. [Genetic study of spinocerebellar hereditary degenerations in Tunisia. Role of consanguinity in their occurrence].
    Ben Hamida M, Chaabouni H, Madani S, Boussen S, Samoud S, Letaief F, Mrabet A, Hentati F, Miladi N.
    J Genet Hum; 1986 Aug; 34(3-4):267-74. PubMed ID: 3760830
    [Abstract] [Full Text] [Related]

  • 31. A spinocerebellar degeneration with X-linked inheritance.
    Spira PJ, McLeod JG, Evans WA.
    Brain; 1979 Mar; 102(1):27-41. PubMed ID: 427531
    [Abstract] [Full Text] [Related]

  • 32. Electron microscopic studies of primary band-shaped keratopathy and gelatinous, drop-like corneal dystrophy in two brothers.
    Kanai A, Kaufman HE.
    Ann Ophthalmol; 1982 Jun; 14(6):535-9. PubMed ID: 6981369
    [Abstract] [Full Text] [Related]

  • 33.
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  • 34.
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  • 35. [Familial corneal degeneration--type Reis-Bücklers (author's transl)].
    Dałkowska A, Pecoldowa K.
    Klin Oczna; 1981 Jun; 83(10-12):515-8. PubMed ID: 6980318
    [No Abstract] [Full Text] [Related]

  • 36. Extrusion of abnormal endothelium into the posterior corneal stroma in a patient with posterior polymorphous dystrophy.
    Feil SH, Barraquer J, Howell DN, Green WR.
    Cornea; 1997 Jul; 16(4):439-46. PubMed ID: 9220242
    [Abstract] [Full Text] [Related]

  • 37.
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  • 38.
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  • 39. Clinical and molecular characterization of a family with autosomal recessive cornea plana.
    Ebenezer ND, Patel CB, Hariprasad SM, Chen LL, Patel RJ, Hardcastle AJ, Allen RC.
    Arch Ophthalmol; 2005 Sep; 123(9):1248-53. PubMed ID: 16157807
    [Abstract] [Full Text] [Related]

  • 40. Ataxia-deafness-retardation syndrome in three sisters.
    Koletzko S, Koletzko B, Lamprecht A, Lenard HG.
    Neuropediatrics; 1987 Feb; 18(1):18-21. PubMed ID: 3470627
    [Abstract] [Full Text] [Related]

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