BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 2043573)

  • 1. Dominant cone dystrophy starting with blue cone involvement.
    van Schooneveld MJ; Went LN; Oosterhuis JA
    Br J Ophthalmol; 1991 Jun; 75(6):332-6. PubMed ID: 2043573
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal dominantly inherited macular dystrophy with preferential short-wavelength sensitive cone involvement.
    Bresnick GH; Smith VC; Pokorny J
    Am J Ophthalmol; 1989 Sep; 108(3):265-76. PubMed ID: 2789001
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Late onset dominant cone dystrophy with early blue cone involvement.
    Went LN; van Schooneveld MJ; Oosterhuis JA
    J Med Genet; 1992 May; 29(5):295-8. PubMed ID: 1583655
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cone and rod function in cone degenerations.
    Sadowski B; Zrenner E
    Vision Res; 1997 Aug; 37(16):2303-14. PubMed ID: 9578911
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Atypical vitelliform macular dystrophy in a 5-generation family.
    Hittner HM; Ferrell RE; Borda RP; Justice J
    Br J Ophthalmol; 1984 Mar; 68(3):199-207. PubMed ID: 6607743
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Differential diagnosis of cone dystrophies].
    Sadowski B; Zrenner E
    Ophthalmologe; 1994 Dec; 91(6):719-29. PubMed ID: 7849422
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Bull's eye maculopathy with early cone degeneration.
    Grey RH; Blach RK; Barnard WM
    Br J Ophthalmol; 1977 Nov; 61(11):702-18. PubMed ID: 588526
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evolution of benign concentric annular macular dystrophy.
    van den Biesen PR; Deutman AF; Pinckers AJ
    Am J Ophthalmol; 1985 Jul; 100(1):73-8. PubMed ID: 4014382
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Blue cone monochromasia: diagnosis, genetic counseling and optical aids].
    Zrenner E; Magnussen S; Lorenz B
    Klin Monbl Augenheilkd; 1988 Nov; 193(5):510-7. PubMed ID: 3264866
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Colour vision, ophthalmological and linkage studies in a pedigree with a tritan defect.
    Went LN; Völker-Dieben H; de Vries-de Mol EC
    Mod Probl Ophthalmol; 1974; 13(0):272-6. PubMed ID: 4548144
    [No Abstract]   [Full Text] [Related]  

  • 11. Color matches in diseased eyes with good acuity: detection of deficits in cone optical density and in chromatic discrimination.
    Swanson WH; Fish GE
    J Opt Soc Am A Opt Image Sci Vis; 1995 Oct; 12(10):2230-6. PubMed ID: 7500203
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Occult macular dystrophy.
    Miyake Y; Horiguchi M; Tomita N; Kondo M; Tanikawa A; Takahashi H; Suzuki S; Terasaki H
    Am J Ophthalmol; 1996 Nov; 122(5):644-53. PubMed ID: 8909203
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [The properties of visual functions and familial analysis in blue cone monochromatism].
    Terasaki H; Miyake Y
    Nippon Ganka Gakkai Zasshi; 1992 Apr; 96(4):523-30. PubMed ID: 1621595
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rod-cone dystrophy of the retina. Continuation of a family study described in 1923.
    Forsius H; Erkkilä H; Eriksson AW
    Acta Ophthalmol (Copenh); 1990 Feb; 68(1):2-10. PubMed ID: 2336929
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases.
    Nishiguchi KM; Sandberg MA; Gorji N; Berson EL; Dryja TP
    Hum Mutat; 2005 Mar; 25(3):248-58. PubMed ID: 15712225
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Progressive generalized cone dysfunction.
    François J; de Rouck A; Verriest G; de Laey JJ; Cambie E
    Ophthalmologica; 1974; 169(4):255-84. PubMed ID: 4547582
    [No Abstract]   [Full Text] [Related]  

  • 17. Association of acquired color vision defects in blue cone monochromatism.
    Terasaki H; Miyake Y
    Jpn J Ophthalmol; 1995; 39(1):55-9. PubMed ID: 7643484
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cone dystrophy or macular dystrophy associated with novel autosomal dominant
    Manes G; Mamouni S; Hérald E; Richard AC; Sénéchal A; Aouad K; Bocquet B; Meunier I; Hamel CP
    Mol Vis; 2017; 23():198-209. PubMed ID: 28442884
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Residual colour detection abilities in age-related macular degeneration.
    Shima N; Markowitz SN; Reyes SV
    Can J Ophthalmol; 2013 Aug; 48(4):274-8. PubMed ID: 23931466
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dominant cone-rod dystrophy.
    Hittner HM; Murphree AL; Garcia CA; Justice J; Chokshi DB
    Doc Ophthalmol; 1975 Nov; 39(1):29-52. PubMed ID: 1201699
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.