BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1973 related articles for article (PubMed ID: 11825021)

  • 1. Concentric retinitis pigmentosa: clinicopathologic correlations.
    Milam AH; De Castro EB; Smith JE; Tang WX; John SK; Gorin MB; Stone EM; Aguirre GD; Jacobson SG
    Exp Eye Res; 2001 Oct; 73(4):493-508. PubMed ID: 11825021
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal dominant retinitis pigmentosa caused by the threonine-17-methionine rhodopsin mutation: retinal histopathology and immunocytochemistry.
    Li ZY; Jacobson SG; Milam AH
    Exp Eye Res; 1994 Apr; 58(4):397-408. PubMed ID: 7925677
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene.
    Jacobson SG; Buraczynska M; Milam AH; Chen C; Järvaläinen M; Fujita R; Wu W; Huang Y; Cideciyan AV; Swaroop A
    Invest Ophthalmol Vis Sci; 1997 Sep; 38(10):1983-97. PubMed ID: 9331262
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinicopathologic effects of the Q64ter rhodopsin mutation in retinitis pigmentosa.
    Milam AH; Li ZY; Cideciyan AV; Jacobson SG
    Invest Ophthalmol Vis Sci; 1996 Apr; 37(5):753-65. PubMed ID: 8603860
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Degenerative changes in a retina affected with autosomal dominant retinitis pigmentosa.
    Flannery JG; Farber DB; Bird AC; Bok D
    Invest Ophthalmol Vis Sci; 1989 Feb; 30(2):191-211. PubMed ID: 2914751
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Normal central retinal function and structure preserved in retinitis pigmentosa.
    Jacobson SG; Roman AJ; Aleman TS; Sumaroka A; Herrera W; Windsor EA; Atkinson LA; Schwartz SB; Steinberg JD; Cideciyan AV
    Invest Ophthalmol Vis Sci; 2010 Feb; 51(2):1079-85. PubMed ID: 19797198
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Histopathologic study of an unusual form of retinitis pigmentosa.
    Szamier RB; Berson EL
    Invest Ophthalmol Vis Sci; 1982 May; 22(5):559-70. PubMed ID: 7076403
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Autosomal dominant retinitis pigmentosa in a large family: a clinical and molecular genetic study.
    Rosas DJ; Roman AJ; Weissbrod P; Macke JP; Nathans J
    Invest Ophthalmol Vis Sci; 1994 Jul; 35(8):3134-44. PubMed ID: 8045708
    [TBL] [Abstract][Full Text] [Related]  

  • 9. X-linked retinitis pigmentosa: functional phenotype of an RP2 genotype.
    Jacobson SG; Roman AJ; Cideciyan AV; Robey MG; Iwata T; Inana G
    Invest Ophthalmol Vis Sci; 1992 Dec; 33(13):3481-92. PubMed ID: 1464493
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosa.
    Jacobson SG; Cideciyan AV; Iannaccone A; Weleber RG; Fishman GA; Maguire AM; Affatigato LM; Bennett J; Pierce EA; Danciger M; Farber DB; Stone EM
    Invest Ophthalmol Vis Sci; 2000 Jun; 41(7):1898-908. PubMed ID: 10845615
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15.
    Demirci FY; Gupta N; Radak AL; Rigatti BW; Mah TS; Milam AH; Gorin MB
    Am J Ophthalmol; 2005 Feb; 139(2):386-8. PubMed ID: 15734019
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Loss of cone molecular markers in rhodopsin-mutant human retinas with retinitis pigmentosa.
    John SK; Smith JE; Aguirre GD; Milam AH
    Mol Vis; 2000 Nov; 6():204-15. PubMed ID: 11063754
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Yearly rates of rod and cone functional loss in retinitis pigmentosa and cone-rod dystrophy.
    Birch DG; Anderson JL; Fish GE
    Ophthalmology; 1999 Feb; 106(2):258-68. PubMed ID: 9951474
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A frameshift mutation in RPGR exon ORF15 causes photoreceptor degeneration and inner retina remodeling in a model of X-linked retinitis pigmentosa.
    Beltran WA; Hammond P; Acland GM; Aguirre GD
    Invest Ophthalmol Vis Sci; 2006 Apr; 47(4):1669-81. PubMed ID: 16565408
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical-ultrastructural study of a retinal dystrophy.
    Bunt-Milam AH; Kalina RE; Pagon RA
    Invest Ophthalmol Vis Sci; 1983 Apr; 24(4):458-69. PubMed ID: 6682096
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Retinal histopathology of an XLRP carrier with a mutation in the RPGR exon ORF15.
    Aguirre GD; Yashar BM; John SK; Smith JE; Breuer DK; Hiriyanna S; Swaroop A; Milam AH
    Exp Eye Res; 2002 Oct; 75(4):431-43. PubMed ID: 12387791
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Correlation of fundus autofluorescence with photoreceptor morphology and functional changes in eyes with retinitis pigmentosa.
    Wakabayashi T; Sawa M; Gomi F; Tsujikawa M
    Acta Ophthalmol; 2010 Aug; 88(5):e177-83. PubMed ID: 20491687
    [TBL] [Abstract][Full Text] [Related]  

  • 18. RP cone-rod degeneration.
    Heckenlively JR
    Trans Am Ophthalmol Soc; 1987; 85():438-70. PubMed ID: 3447340
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Patterns of visual field progression in patients with retinitis pigmentosa.
    Grover S; Fishman GA; Brown J
    Ophthalmology; 1998 Jun; 105(6):1069-75. PubMed ID: 9627658
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Sex-linked retinitis pigmentosa: ultrastructure of photoreceptors and pigment epithelium.
    Szamier RB; Berson EL; Klein R; Meyers S
    Invest Ophthalmol Vis Sci; 1979 Feb; 18(2):145-60. PubMed ID: 761969
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 99.