BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

402 related articles for article (PubMed ID: 18641288)

  • 1. Disease course in patients with autosomal recessive retinitis pigmentosa due to the USH2A gene.
    Sandberg MA; Rosner B; Weigel-DiFranco C; McGee TL; Dryja TP; Berson EL
    Invest Ophthalmol Vis Sci; 2008 Dec; 49(12):5532-9. PubMed ID: 18641288
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations.
    Sandberg MA; Rosner B; Weigel-DiFranco C; Dryja TP; Berson EL
    Invest Ophthalmol Vis Sci; 2007 Mar; 48(3):1298-304. PubMed ID: 17325176
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Visual Prognosis in USH2A-Associated Retinitis Pigmentosa Is Worse for Patients with Usher Syndrome Type IIa Than for Those with Nonsyndromic Retinitis Pigmentosa.
    Pierrache LH; Hartel BP; van Wijk E; Meester-Smoor MA; Cremers FP; de Baere E; de Zaeytijd J; van Schooneveld MJ; Cremers CW; Dagnelie G; Hoyng CB; Bergen AA; Leroy BP; Pennings RJ; van den Born LI; Klaver CC
    Ophthalmology; 2016 May; 123(5):1151-60. PubMed ID: 26927203
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Correlation between Genotype and Phenotype in 69 Chinese Patients with USH2A Mutations: A comparative study of the patients with Usher Syndrome and Nonsyndromic Retinitis Pigmentosa.
    Meng X; Liu X; Li Y; Guo T; Yang L
    Acta Ophthalmol; 2021 Jun; 99(4):e447-e460. PubMed ID: 33124170
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Disease progression in patients with dominant retinitis pigmentosa and rhodopsin mutations.
    Berson EL; Rosner B; Weigel-DiFranco C; Dryja TP; Sandberg MA
    Invest Ophthalmol Vis Sci; 2002 Sep; 43(9):3027-36. PubMed ID: 12202526
    [TBL] [Abstract][Full Text] [Related]  

  • 6. RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosa.
    Sharon D; Sandberg MA; Rabe VW; Stillberger M; Dryja TP; Berson EL
    Am J Hum Genet; 2003 Nov; 73(5):1131-46. PubMed ID: 14564670
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotypic conservation in patients with X-linked retinitis pigmentosa caused by RPGR mutations.
    Zahid S; Khan N; Branham K; Othman M; Karoukis AJ; Sharma N; Moncrief A; Mahmood MN; Sieving PA; Swaroop A; Heckenlively JR; Jayasundera T
    JAMA Ophthalmol; 2013 Aug; 131(8):1016-25. PubMed ID: 23681342
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Visual Outcomes in Japanese Patients with Retinitis Pigmentosa and Usher Syndrome Caused by USH2A Mutations.
    Nagase Y; Kurata K; Hosono K; Suto K; Hikoya A; Nakanishi H; Mizuta K; Mineta H; Minoshima S; Hotta Y
    Semin Ophthalmol; 2018; 33(4):560-565. PubMed ID: 28678594
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Disease course of patients with pericentral retinitis pigmentosa.
    Sandberg MA; Gaudio AR; Berson EL
    Am J Ophthalmol; 2005 Jul; 140(1):100-6. PubMed ID: 15953579
    [TBL] [Abstract][Full Text] [Related]  

  • 10. High Symmetry of Visual Acuity and Visual Fields in RPGR-Linked Retinitis Pigmentosa.
    Bellingrath JS; Ochakovski GA; Seitz IP; Kohl S; Zrenner E; Hanig N; Prokisch H; Weber BH; Downes SM; Ramsden S; MacLaren RE; Fischer MD
    Invest Ophthalmol Vis Sci; 2017 Sep; 58(11):4457-4466. PubMed ID: 28863407
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical and Electrophysiologic Characteristics of a Large Kindred with X-Linked Retinitis Pigmentosa Associated with the RPGR Locus.
    Tzu JH; Arguello T; Berrocal AM; Berrocal M; Weisman AD; Liu M; Hess D; Caputo M; Goldberg JL; Feuer WJ; Stone EM; Lam BL
    Ophthalmic Genet; 2015; 36(4):321-6. PubMed ID: 24555744
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Visual Function in Carriers of X-Linked Retinitis Pigmentosa.
    Comander J; Weigel-DiFranco C; Sandberg MA; Berson EL
    Ophthalmology; 2015 Sep; 122(9):1899-906. PubMed ID: 26143542
    [TBL] [Abstract][Full Text] [Related]  

  • 13. X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual function.
    Sharon D; Bruns GA; McGee TL; Sandberg MA; Berson EL; Dryja TP
    Invest Ophthalmol Vis Sci; 2000 Aug; 41(9):2712-21. PubMed ID: 10937588
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical course, genetic etiology, and visual outcome in cone and cone-rod dystrophy.
    Thiadens AA; Phan TM; Zekveld-Vroon RC; Leroy BP; van den Born LI; Hoyng CB; Klaver CC; ; Roosing S; Pott JW; van Schooneveld MJ; van Moll-Ramirez N; van Genderen MM; Boon CJ; den Hollander AI; Bergen AA; De Baere E; Cremers FP; Lotery AJ
    Ophthalmology; 2012 Apr; 119(4):819-26. PubMed ID: 22264887
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The relationship between visual field size and electroretinogram amplitude in retinitis pigmentosa.
    Sandberg MA; Weigel-DiFranco C; Rosner B; Berson EL
    Invest Ophthalmol Vis Sci; 1996 Jul; 37(8):1693-8. PubMed ID: 8675413
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and preclinical therapeutic outcome metrics for USH2A-related disease.
    Toms M; Dubis AM; de Vrieze E; Tracey-White D; Mitsios A; Hayes M; Broekman S; Baxendale S; Utoomprurkporn N; Bamiou D; Bitner-Glindzicz M; Webster AR; Van Wijk E; Moosajee M
    Hum Mol Genet; 2020 Jul; 29(11):1882-1899. PubMed ID: 31998945
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Screen of the IMPDH1 gene among patients with dominant retinitis pigmentosa and clinical features associated with the most common mutation, Asp226Asn.
    Wada Y; Sandberg MA; McGee TL; Stillberger MA; Berson EL; Dryja TP
    Invest Ophthalmol Vis Sci; 2005 May; 46(5):1735-41. PubMed ID: 15851576
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cone Structure and Function in RPGR- and USH2A-Associated Retinal Degeneration.
    Micevych PS; Wong J; Zhou H; Wang RK; Porco TC; Carroll J; Roorda A; Duncan JL
    Am J Ophthalmol; 2023 Jun; 250():1-11. PubMed ID: 36646238
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Disease course of patients with unilateral pigmentary retinopathy.
    Potsidis E; Berson EL; Sandberg MA
    Invest Ophthalmol Vis Sci; 2011 Nov; 52(12):9244-9. PubMed ID: 21989720
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1).
    Berson EL; Grimsby JL; Adams SM; McGee TL; Sweklo E; Pierce EA; Sandberg MA; Dryja TP
    Invest Ophthalmol Vis Sci; 2001 Sep; 42(10):2217-24. PubMed ID: 11527933
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.