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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 4924455)

  • 1. Hereditary granular corneal dystrophy and associated aminoaciduria.
    Potter D; Mattingley J
    Trans Aust Coll Ophthalmol; 1969; 1():45-52. PubMed ID: 4924455
    [No Abstract]   [Full Text] [Related]  

  • 2. Severe granular dystrophy: a pedigree with presumed homozygotes.
    Diaper CJ
    Eye (Lond); 1994; 8 ( Pt 4)():448-52. PubMed ID: 7821471
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [Groenouw I type dystrophy in its diffuse superficial form].
    Pouliquen Y; Dhermy P; Monteil C; Legras M
    Bull Mem Soc Fr Ophtalmol; 1977; 89():327-35. PubMed ID: 305799
    [No Abstract]   [Full Text] [Related]  

  • 5. Adult polycystic kidney disease and lattice corneal dystrophy: occurrence in a single family.
    Whitt JW; Wood BC; Sharma JN; Crouch TT
    Arch Intern Med; 1978 Jul; 138(7):1167-8. PubMed ID: 307373
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital hereditary endothelial dystrophy.
    Collum LM; Lavin J; Mullaney J
    Bull Soc Belge Ophtalmol; 1984; 211():1-5. PubMed ID: 6336261
    [No Abstract]   [Full Text] [Related]  

  • 7. [Reis-Bücklers corneal dystrophy and the role of Bowman's membrane].
    Winkelman JE; Delleman JW
    Klin Monbl Augenheilkd; 1969 Sep; 155(3):380-7. PubMed ID: 4901272
    [No Abstract]   [Full Text] [Related]  

  • 8. [A hitherto unknown subepithelial hereditary corneal dystrophy].
    Thiel HJ; Behnke H
    Klin Monbl Augenheilkd; 1967; 150(6):862-74. PubMed ID: 5301630
    [No Abstract]   [Full Text] [Related]  

  • 9. [Corneal macular dystrophy in Finland].
    Meretoja J
    Duodecim; 1977; 93(13):902-6. PubMed ID: 303983
    [No Abstract]   [Full Text] [Related]  

  • 10. Hereditary crystalline corneal dystrophy with an associated blood lipid disorder.
    Williams HP; Bron AJ; Tripathi RC; Garner A
    Trans Ophthalmol Soc U K (1962); 1971; 91():531-41. PubMed ID: 5316991
    [No Abstract]   [Full Text] [Related]  

  • 11. Analysis of human transforming growth factor beta-induced gene mutation in corneal dystrophy.
    Li Y; Sun XG; Ren HY; Dong B; Wang ZQ; Sun XY
    Chin Med J (Engl); 2004 Sep; 117(9):1418-21. PubMed ID: 15377440
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Identification of BIGH3 gene mutations in the patients with two types of corneal dystrophies].
    Jin T; Zou LH; Yang L; Dong WL; Yu J; Lu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):32-4. PubMed ID: 14767905
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [A new family of granulous corneal dystrophy (Groenouw I)].
    Scouras J; Cuendet JF; Streiff EB
    J Genet Hum; 1969 Oct; 17(3):471-4. PubMed ID: 5311773
    [No Abstract]   [Full Text] [Related]  

  • 14. [Hereditary hyalin degeneration of the cornea].
    Pinckers A
    Ann Ocul (Paris); 1971 Mar; 204(3):271-8. PubMed ID: 5314510
    [No Abstract]   [Full Text] [Related]  

  • 15. In vivo laser confocal microscopy findings for Bowman's layer dystrophies (Thiel-Behnke and Reis-Bücklers corneal dystrophies).
    Kobayashi A; Sugiyama K
    Ophthalmology; 2007 Jan; 114(1):69-75. PubMed ID: 17198850
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Band-shaped elastotic keratopathy (degeneratio corneae spherularis elastoides) in familial corneal dystrophy].
    Stefani FH; Lorenz B; Neubauer L; Hildebrand-Krückmann IH
    Fortschr Ophthalmol; 1987; 84(2):126-30. PubMed ID: 3496261
    [No Abstract]   [Full Text] [Related]  

  • 17. [Histopathological study of familial systemic amyloidosis with latticed corneal dystrophy].
    Wang SJ
    Zhonghua Yi Xue Za Zhi; 1985 Feb; 65(2):78-9. PubMed ID: 3921213
    [No Abstract]   [Full Text] [Related]  

  • 18. Clinical and immunopathological corneal phenotype in homozygotes for the BIGH3 R124H mutation.
    Diaper CJ; Schorderet DF; Chaubert P; Munier FL
    Eye (Lond); 2005 Jan; 19(1):92-6. PubMed ID: 15094731
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Dominant hereditary early infantile progressive endothelial corneal dystrophy (horseshoe-shaped beginning variant of Schlichting's endothelial dystrophy)].
    Jaeger W; Sundmacher R; Witschel H; Stangl R
    Buch Augenarzt; 1982; 88():108-15. PubMed ID: 6979374
    [No Abstract]   [Full Text] [Related]  

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

    [Next]    [New Search]
    of 7.