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Journal Abstract Search

297 related items for PubMed ID: 4132515

  • 1. [Lattice dystrophy. Primary and familial localized corneal amyloidosis].
    Dhermy P, Brégeat P, Hamard H, Rizman P, Offret H.
    Arch Ophtalmol Rev Gen Ophtalmol; 1973; 33(6):477-84. PubMed ID: 4132515
    [No Abstract] [Full Text] [Related]

  • 2. [Electron microscopic study of a Haab-Dimmer lattice dystrophy].
    Pouliquen Y, Dhermy P, Taillebourg O.
    Arch Ophtalmol Rev Gen Ophtalmol; 1973; 33(6):485-99. PubMed ID: 4132516
    [No Abstract] [Full Text] [Related]

  • 3. [Reticular dystrophy of the cornea. A form of hereditary-familial amyloidosis].
    Garrido C, Malbran E, Stefani C.
    Arch Oftalmol B Aires; 1968 Jun; 43(6):139-45. PubMed ID: 4181889
    [No Abstract] [Full Text] [Related]

  • 4. Granular-lattice (Avellino) corneal dystrophy in Japanese patients.
    Konishi M, Mashima Y, Nakamura Y, Yamada M, Sugiura H.
    Cornea; 1997 Nov; 16(6):635-8. PubMed ID: 9395872
    [Abstract] [Full Text] [Related]

  • 5.
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  • 6. [General amyloidosis with lattice dystrophy of the cornea].
    Meretoja J.
    Duodecim; 1971 Nov; 87(21):1412-9. PubMed ID: 5315643
    [No Abstract] [Full Text] [Related]

  • 7. Current concepts on the ultrastructural pathogenesis of macular and lattice corneal dystrophies.
    Klintworth GK.
    Birth Defects Orig Artic Ser; 1971 Mar; 7(3):27-31. PubMed ID: 4141632
    [Abstract] [Full Text] [Related]

  • 8. Light microscopical and polarisation optical study of the lattice dystrophy of the cornea.
    François J, Fehér J.
    Ophthalmologica; 1972 Mar; 164(1):1-18. PubMed ID: 4536878
    [No Abstract] [Full Text] [Related]

  • 9. [A case of familial corneal dystrophy. Clinical, histological and ultrastructural study].
    Offret G, Pouliquen Y, Coscas G.
    Arch Ophtalmol Rev Gen Ophtalmol; 1969 Mar; 29(6):537-50. PubMed ID: 4186843
    [No Abstract] [Full Text] [Related]

  • 10. Primary familial amyloidosis of the cornea.
    Kirk HQ, Rabb M, Hattenhauer J, Smith R.
    Trans Am Acad Ophthalmol Otolaryngol; 1973 Mar; 77(4):OP411-7. PubMed ID: 4126001
    [No Abstract] [Full Text] [Related]

  • 11.
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  • 12. Lattice corneal dystrophy. An inherited variety of amyloidosis restricted to the cornea.
    Klintworth GK.
    Am J Pathol; 1967 Mar; 50(3):371-99. PubMed ID: 4163628
    [No Abstract] [Full Text] [Related]

  • 13. Atypical corneal dystrophy with stromal amyloid deposits.
    Malbran ES, Meijide RF, Croxatto JO.
    Cornea; 1988 Mar; 7(3):210-3. PubMed ID: 3048883
    [Abstract] [Full Text] [Related]

  • 14. [Metabolic disorders and corneal changes (author's transl)].
    François J.
    Klin Monbl Augenheilkd; 1981 Jun; 178(6):419-23. PubMed ID: 6973662
    [Abstract] [Full Text] [Related]

  • 15. [Meretoja syndrome: Identification of a family and description of the corneal involvement by confocal microscopy].
    Bonnin N, Borel A, Daniel E, Tiple A, Joubert R, Heng AE, Chiambaretta F.
    J Fr Ophtalmol; 2015 Jun; 38(6):e111-5. PubMed ID: 25913657
    [No Abstract] [Full Text] [Related]

  • 16. Unilateral lattice dystrophy of the cornea.
    Rabb MF, Blodi F, Boniuk M.
    Trans Am Acad Ophthalmol Otolaryngol; 1974 Jun; 78(3):OP440-4. PubMed ID: 4546187
    [No Abstract] [Full Text] [Related]

  • 17. Hereditary amyloidosis of the cornea.
    Garner A.
    J Pathol; 1970 Feb; 100(2):Pvi. PubMed ID: 5310277
    [No Abstract] [Full Text] [Related]

  • 18. [Focus on an anatomoclinical entity: Biber-Haab-Dimmer lattice dystrophy].
    Durand L, Resal R, Burillon C.
    J Fr Ophtalmol; 1985 Feb; 8(11):729-34. PubMed ID: 3914501
    [Abstract] [Full Text] [Related]

  • 19. TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosis.
    Takács L, Losonczy G, Matesz K, Balogh I, Sohajda Z, Tóth K, Fazakas F, Vereb G, Berta A.
    Mol Vis; 2007 Oct 18; 13():1976-83. PubMed ID: 17982422
    [Abstract] [Full Text] [Related]

  • 20.
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