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 *

57 related articles for article (PubMed ID: 9606569)

  • 1. Recent advances in the genetics of macular dystrophies.
    Mah DY; Wong PW; Edwards A; MacDonald IM
    Can J Ophthalmol; 1998 Apr; 33(3):135-43. PubMed ID: 9606569
    [No Abstract]   [Full Text] [Related]  

  • 2. Diagnostic issues with inherited retinal and macular dystrophies.
    Sieving PA
    Semin Ophthalmol; 1995 Dec; 10(4):279-94. PubMed ID: 10160215
    [No Abstract]   [Full Text] [Related]  

  • 3. The challenge of modeling macular degeneration in mice.
    Marmorstein AD; Marmorstein LY
    Trends Genet; 2007 May; 23(5):225-31. PubMed ID: 17368622
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Choroidal neovascularization in a patient with adult foveomacular dystrophy and a mutation in the retinal degeneration slow gene (Pro 210 Arg).
    Feist RM; White MF; Skalka H; Stone EM
    Am J Ophthalmol; 1994 Aug; 118(2):259-60. PubMed ID: 7519821
    [No Abstract]   [Full Text] [Related]  

  • 5. Is successful gene therapy for retinal disease in sight?
    Caplen NJ
    Mol Med Today; 2000 Sep; 6(9):340. PubMed ID: 11202971
    [No Abstract]   [Full Text] [Related]  

  • 6. Novel human pathological mutations. Gene symbol: RDS. Disease: macular dystrophy.
    Villaverde C; Trujillo-Tiebas MJ; Gallego-Merlo J; Vallespin E; Cantalapiedra D; Riveiro-Alvarez R; Carballo M; Ayuso C
    Hum Genet; 2007 Dec; 122(5):555. PubMed ID: 18383606
    [No Abstract]   [Full Text] [Related]  

  • 7. Diagnostic and therapeutic challenges. Bilateral reduction in central visual function.
    McDonald HR
    Retina; 1999; 19(3):242-5. PubMed ID: 10380031
    [No Abstract]   [Full Text] [Related]  

  • 8. Diagnostic and therapeutic challenges.
    Schatz H
    Retina; 2003 Aug; 23(4):530-5. PubMed ID: 12972766
    [No Abstract]   [Full Text] [Related]  

  • 9. Focus on molecules: RDS.
    Conley SM; Naash MI
    Exp Eye Res; 2009 Sep; 89(3):278-9. PubMed ID: 19366620
    [No Abstract]   [Full Text] [Related]  

  • 10. [Hereditary macular dystrophies].
    Rozet JM; Gerber S; Ducroq D; Hamel C; Dufier JL; Kaplan J
    J Fr Ophtalmol; 2005 Jan; 28(1):113-24. PubMed ID: 15767907
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea.
    Nichols BE; Drack AV; Vandenburgh K; Kimura AE; Sheffield VC; Stone EM
    Hum Mol Genet; 1993 May; 2(5):601-3. PubMed ID: 8251014
    [No Abstract]   [Full Text] [Related]  

  • 12. Nucleotide and predicted protein sequence of rat retinal degeneration slow (rds).
    Begy C; Bridges CD
    Nucleic Acids Res; 1990 May; 18(10):3058. PubMed ID: 2349107
    [No Abstract]   [Full Text] [Related]  

  • 13. Genetic determinants of visual functions.
    Deeb SS
    Curr Opin Neurobiol; 1993 Aug; 3(4):506-12. PubMed ID: 8219717
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gene therapy for retinal degeneration.
    Reichel MB; Ali RR; Hunt DM; Bhattacharya SS
    Ophthalmic Res; 1997; 29(5):261-8. PubMed ID: 9323717
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Peripherin and the vision thing.
    Davies K
    Nature; 1993 Mar; 362(6415):92. PubMed ID: 8446174
    [No Abstract]   [Full Text] [Related]  

  • 16. Tulp1 is involved in specific photoreceptor protein transport pathways.
    Hagstrom SA; Watson RF; Pauer GJ; Grossman GH
    Adv Exp Med Biol; 2012; 723():783-9. PubMed ID: 22183407
    [No Abstract]   [Full Text] [Related]  

  • 17. Genotype-phenotype correlations and differential diagnosis in autosomal dominant macular disease.
    Iannaccone A
    Doc Ophthalmol; 2001 May; 102(3):197-236. PubMed ID: 11556486
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Hereditary retinal dystrophies].
    Kellner U
    Ophthalmologe; 1997 Feb; 94(2):164-83. PubMed ID: 9156644
    [No Abstract]   [Full Text] [Related]  

  • 19. A medley of retinal dystrophies.
    Travis GH; Hepler JE
    Nat Genet; 1993 Mar; 3(3):191-2. PubMed ID: 8485572
    [No Abstract]   [Full Text] [Related]  

  • 20. Name dropping.
    Travis GH
    Nature; 1991 Jan; 349(6304):24. PubMed ID: 1985259
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.