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Journal Abstract Search

126 related items for PubMed ID: 23463886

  • 1. Severity of familial isolated retinitis pigmentosa across different inheritance patterns among an Asian Indian cohort.
    Bende P, Natarajan K, Marudhamuthu T, Madhavan J.
    J Pediatr Ophthalmol Strabismus; 2013; 50(1):34-6. PubMed ID: 23463886
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  • 2. Expanded Retinal Disease Spectrum Associated With Autosomal Recessive Mutations in GUCY2D.
    Stunkel ML, Brodie SE, Cideciyan AV, Pfeifer WL, Kennedy EL, Stone EM, Jacobson SG, Drack AV.
    Am J Ophthalmol; 2018 Jun; 190():58-68. PubMed ID: 29559409
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  • 3. A novel mutation in retinitis pigmentosa GTPase regulator gene with a distinctive retinitis pigmentosa phenotype in a Chinese family.
    Sheng X, Li Z, Zhang X, Wang J, Ren H, Sun Y, Meng R, Rong W, Zhuang W.
    Mol Vis; 2010 Aug 15; 16():1620-8. PubMed ID: 20806050
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  • 4. Clinical and genetic findings of a Japanese patient with RP1-related autosomal recessive retinitis pigmentosa.
    Kurata K, Hosono K, Hotta Y.
    Doc Ophthalmol; 2018 Aug 15; 137(1):47-56. PubMed ID: 30027431
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  • 12. Evidence for a novel autosomal dominant retinitis pigmentosa linked to chromosome 1p22.1-q12 in a Chinese family.
    Yuan Y, Zhou X, Wang F, Yan M, Ding F.
    Curr Eye Res; 2011 Feb 15; 36(2):154-67. PubMed ID: 21281067
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  • 13. Pedigree Analysis of Families and Patients Affected by Retinitis Pigmentosa.
    Scherbakova I, Ragi SD.
    Methods Mol Biol; 2023 Feb 15; 2560():67-71. PubMed ID: 36481883
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  • 14. Visual acuity impairment in patients with retinitis pigmentosa.
    Grover S, Fishman GA, Alexander KR, Anderson RJ, Derlacki DJ.
    Ophthalmology; 1996 Oct 15; 103(10):1593-600. PubMed ID: 8874431
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  • 19. Risk factors for genetic typing and detection in retinitis pigmentosa.
    Berson EL, Rosner B, Simonoff E.
    Am J Ophthalmol; 1980 Jun 15; 89(6):763-75. PubMed ID: 6966889
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  • 20. Retinitis pigmentosa. Genetic percentages.
    Fishman GA.
    Arch Ophthalmol; 1978 May 15; 96(5):822-6. PubMed ID: 655919
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