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Journal Abstract Search

504 related items for PubMed ID: 32675063

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  • 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
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  • 6. Whole exome sequencing identifies novel USH2A mutations and confirms Usher syndrome 2 diagnosis in Chinese retinitis pigmentosa patients.
    Ng TK, Tang W, Cao Y, Chen S, Zheng Y, Xiao X, Chen H.
    Sci Rep; 2019 Apr 04; 9(1):5628. PubMed ID: 30948794
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  • 7. USH2A gene variants cause Keratoconus and Usher syndrome phenotypes in Pakistani families.
    Ahmed AN, Tahir R, Khan N, Ahmad M, Dawood M, Basit A, Yasin M, Nowshid M, Marwan M, Sultan K, Saleha S.
    BMC Ophthalmol; 2021 Apr 29; 21(1):191. PubMed ID: 33926394
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  • 8. USH2A mutational spectrum causing syndromic and non-syndromic retinal dystrophies in a large cohort of Mexican patients.
    Ordoñez-Labastida V, Chacon-Camacho OF, Lopez-Rodriguez VR, Zenteno JC.
    Mol Vis; 2023 Apr 29; 29():31-38. PubMed ID: 37287646
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  • 11. Targeted next-generation sequencing reveals novel USH2A mutations associated with diverse disease phenotypes: implications for clinical and molecular diagnosis.
    Chen X, Sheng X, Liu X, Li H, Liu Y, Rong W, Ha S, Liu W, Kang X, Zhao K, Zhao C.
    PLoS One; 2014 Apr 29; 9(8):e105439. PubMed ID: 25133613
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  • 12. Truncating Variants Contribute to Hearing Loss and Severe Retinopathy in USH2A-Associated Retinitis Pigmentosa in Japanese Patients.
    Inaba A, Maeda A, Yoshida A, Kawai K, Hirami Y, Kurimoto Y, Kosugi S, Takahashi M.
    Int J Mol Sci; 2020 Oct 22; 21(21):. PubMed ID: 33105608
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  • 13. Prevalence and genetic-phenotypic characteristics of patients with USH2A mutations in a large cohort of Chinese patients with inherited retinal disease.
    Gao FJ, Wang DD, Chen F, Sun HX, Hu FY, Xu P, Li J, Liu W, Qi YH, Li W, Wang M, Zhang S, Xu GZ, Chang Q, Wu JH.
    Br J Ophthalmol; 2021 Jan 22; 105(1):87-92. PubMed ID: 32188678
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  • 14. Seven novel mutations in the long isoform of the USH2A gene in Chinese families with nonsyndromic retinitis pigmentosa and Usher syndrome Type II.
    Xu W, Dai H, Lu T, Zhang X, Dong B, Li Y.
    Mol Vis; 2011 Jan 22; 17():1537-52. PubMed ID: 21686329
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  • 15. Identification of five novel mutations in the long isoform of the USH2A gene in Chinese families with Usher syndrome type II.
    Dai H, Zhang X, Zhao X, Deng T, Dong B, Wang J, Li Y.
    Mol Vis; 2008 Jan 22; 14():2067-75. PubMed ID: 19023448
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  • 20. Identification of novel USH2A mutations in patients with autosomal recessive retinitis pigmentosa via targeted next‑generation sequencing.
    Zhu X, Li X, Tian W, Yang Y, Sun K, Li S, Zhu X.
    Mol Med Rep; 2020 Jul 22; 22(1):193-200. PubMed ID: 32319668
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