BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

264 related articles for article (PubMed ID: 29528978)

  • 1. CLINICAL AND GENETIC CHARACTERISTICS OF MALE PATIENTS WITH RPGR-ASSOCIATED RETINAL DYSTROPHIES: A Long-Term Follow-up Study.
    Talib M; van Schooneveld MJ; Thiadens AA; Fiocco M; Wijnholds J; Florijn RJ; Schalij-Delfos NE; van Genderen MM; Putter H; Cremers FPM; Dagnelie G; Ten Brink JB; Klaver CCW; van den Born LI; Hoyng CB; Bergen AA; Boon CJF
    Retina; 2019 Jun; 39(6):1186-1199. PubMed ID: 29528978
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotypic and Phenotypic Characteristics of CRB1-Associated Retinal Dystrophies: A Long-Term Follow-up Study.
    Talib M; van Schooneveld MJ; van Genderen MM; Wijnholds J; Florijn RJ; Ten Brink JB; Schalij-Delfos NE; Dagnelie G; Cremers FPM; Wolterbeek R; Fiocco M; Thiadens AA; Hoyng CB; Klaver CC; Bergen AA; Boon CJF
    Ophthalmology; 2017 Jun; 124(6):884-895. PubMed ID: 28341475
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Detailed comparison of phenotype between male patients carrying variants in exons 1-14 and ORF15 of RPGR.
    Zou X; Fang S; Wu S; Li H; Sun Z; Zhu T; Wei X; Sui R
    Exp Eye Res; 2020 Sep; 198():108147. PubMed ID: 32702353
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Genetic Characteristics and Long-Term Follow-Up of Slovenian Patients with RPGR Retinal Dystrophy.
    Hadalin V; Buscarino M; Sajovic J; Meglič A; Jarc-Vidmar M; Hawlina M; Volk M; Fakin A
    Int J Mol Sci; 2023 Feb; 24(4):. PubMed ID: 36835250
    [TBL] [Abstract][Full Text] [Related]  

  • 6.
    Nguyen XT; Talib M; van Schooneveld MJ; Brinks J; Ten Brink J; Florijn RJ; Wijnholds J; Verdijk RM; Bergen AA; Boon CJF
    Int J Mol Sci; 2020 Jan; 21(3):. PubMed ID: 32012938
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Spectrum of Structural and Functional Abnormalities in Female Carriers of Pathogenic Variants in the RPGR Gene.
    Talib M; van Schooneveld MJ; Van Cauwenbergh C; Wijnholds J; Ten Brink JB; Florijn RJ; Schalij-Delfos NE; Dagnelie G; van Genderen MM; De Baere E; Meester-Smoor MA; De Zaeytijd J; Cremers FPM; van den Born LI; Thiadens AA; Hoyng CB; Klaver CC; Leroy BP; Bergen AA; Boon CJF
    Invest Ophthalmol Vis Sci; 2018 Aug; 59(10):4123-4133. PubMed ID: 30105367
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spectrum of Disease Severity in Patients With X-Linked Retinitis Pigmentosa Due to RPGR Mutations.
    Di Iorio V; Karali M; Melillo P; Testa F; Brunetti-Pierri R; Musacchia F; Condroyer C; Neidhardt J; Audo I; Zeitz C; Banfi S; Simonelli F
    Invest Ophthalmol Vis Sci; 2020 Dec; 61(14):36. PubMed ID: 33372982
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Correlation of ultra-widefield fundus autofluorescence patterns with the underlying genotype in retinal dystrophies and retinitis pigmentosa.
    Trichonas G; Traboulsi EI; Ehlers JP
    Ophthalmic Genet; 2017; 38(4):320-324. PubMed ID: 27880076
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Discordant phenotypes in fraternal twins having an identical mutation in exon ORF15 of the RPGR gene.
    Walia S; Fishman GA; Swaroop A; Branham KE; Lindeman M; Othman M; Weleber RG
    Arch Ophthalmol; 2008 Mar; 126(3):379-84. PubMed ID: 18332319
    [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. RPGR-associated retinal degeneration in human X-linked RP and a murine model.
    Huang WC; Wright AF; Roman AJ; Cideciyan AV; Manson FD; Gewaily DY; Schwartz SB; Sadigh S; Limberis MP; Bell P; Wilson JM; Swaroop A; Jacobson SG
    Invest Ophthalmol Vis Sci; 2012 Aug; 53(9):5594-608. PubMed ID: 22807293
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes.
    Andréasson S; Breuer DK; Eksandh L; Ponjavic V; Frennesson C; Hiriyanna S; Filippova E; Yashar BM; Swaroop A
    Ophthalmic Genet; 2003 Dec; 24(4):215-23. PubMed ID: 14566651
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Novel C8orf37 Mutations in Patients with Early-onset Retinal Dystrophy, Macular Atrophy, Cataracts, and High Myopia.
    Katagiri S; Hayashi T; Yoshitake K; Akahori M; Ikeo K; Gekka T; Tsuneoka H; Iwata T
    Ophthalmic Genet; 2016; 37(1):68-75. PubMed ID: 25113443
    [TBL] [Abstract][Full Text] [Related]  

  • 16. X-Chromosome Inactivation Is a Biomarker of Clinical Severity in Female Carriers of RPGR-Associated X-Linked Retinitis Pigmentosa.
    Fahim AT; Sullivan LS; Bowne SJ; Jones KD; Wheaton DKH; Khan NW; Heckenlively JR; Jayasundera KT; Branham KH; Andrews CA; Othman MI; Karoukis AJ; Birch DG; Daiger SP
    Ophthalmol Retina; 2020 May; 4(5):510-520. PubMed ID: 31953110
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical course of cone dystrophy caused by mutations in the RPGR gene.
    Thiadens AA; Soerjoesing GG; Florijn RJ; Tjiam AG; den Hollander AI; van den Born LI; Riemslag FC; Bergen AA; Klaver CC
    Graefes Arch Clin Exp Ophthalmol; 2011 Oct; 249(10):1527-35. PubMed ID: 21866333
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phenotypic Features of Oguchi Disease and Retinitis Pigmentosa in Patients with S-Antigen Mutations: A Long-Term Follow-up Study.
    Nishiguchi KM; Ikeda Y; Fujita K; Kunikata H; Akiho M; Hashimoto K; Hosono K; Kurata K; Koyanagi Y; Akiyama M; Suzuki T; Kawasaki R; Wada Y; Hotta Y; Sonoda KH; Murakami A; Nakazawa M; Nakazawa T; Abe T
    Ophthalmology; 2019 Nov; 126(11):1557-1566. PubMed ID: 31257036
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Long-term clinical course of 2 Japanese patients with PRPF31-related retinitis pigmentosa.
    Kurata K; Hosono K; Hotta Y
    Jpn J Ophthalmol; 2018 Mar; 62(2):186-193. PubMed ID: 29305715
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.