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Journal Abstract Search

326 related items for PubMed ID: 15531314

  • 1. Four Japanese male patients with juvenile retinoschisis: only three have mutations in the RS1 gene.
    Hayashi T, Omoto S, Takeuchi T, Kozaki K, Ueoka Y, Kitahara K.
    Am J Ophthalmol; 2004 Nov; 138(5):788-98. PubMed ID: 15531314
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  • 2. Unusual manifestations of x-linked retinoschisis: clinical profile and diagnostic evaluation.
    Shukla D, Rajendran A, Gibbs D, Suganthalakshmi B, Zhang K, Sundaresan P.
    Am J Ophthalmol; 2007 Sep; 144(3):419-423. PubMed ID: 17631851
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  • 6. Four novel RS1 gene mutations in Polish patients with X-linked juvenile retinoschisis.
    Skorczyk A, Krawczyński MR.
    Mol Vis; 2012 Sep; 18():3004-12. PubMed ID: 23288992
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  • 7. Novel NR2E3 mutations (R104Q, R334G) associated with a mild form of enhanced S-cone syndrome demonstrate compound heterozygosity.
    Hayashi T, Gekka T, Goto-Omoto S, Takeuchi T, Kubo A, Kitahara K.
    Ophthalmology; 2005 Dec; 112(12):2115. PubMed ID: 16225923
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  • 8. Optical coherence tomography in the diagnosis of juvenile X-linked retinoschisis.
    Eriksson U, Larsson E, Holmström G.
    Acta Ophthalmol Scand; 2004 Apr; 82(2):218-23. PubMed ID: 15043546
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  • 9. Correlation of genetic and clinical findings in Spanish patients with X-linked juvenile retinoschisis.
    Riveiro-Alvarez R, Trujillo-Tiebas MJ, Gimenez-Pardo A, Garcia-Hoyos M, Lopez-Martinez MA, Aguirre-Lamban J, Garcia-Sandoval B, Vazquez-Fernandez del Pozo S, Cantalapiedra D, Avila-Fernandez A, Baiget M, Ramos C, Ayuso C.
    Invest Ophthalmol Vis Sci; 2009 Sep; 50(9):4342-50. PubMed ID: 19324861
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  • 10. X-linked retinoschisis--clinical manifestation, genetic and electrophysiological analysis of three generations with p.Arg197Cys mutation of RS1 gene.
    Ulinska M, Kmera-Muszynska M, Szulborski K, Broniek-Kowalik K, Franaszczyk M, Oldak M, Ploski R.
    Klin Oczna; 2014 Sep; 116(3):187-92. PubMed ID: 25799783
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  • 13. Two cases of X-linked juvenile retinoschisis with different optical coherence tomography findings and RS1 gene mutations.
    Chan WM, Choy KW, Wang J, Lam DS, Yip WW, Fu W, Pang CP.
    Clin Exp Ophthalmol; 2004 Aug; 32(4):429-32. PubMed ID: 15281981
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  • 14. An unusual X-linked retinoschisis phenotype and biochemical characterization of the W112C RS1 mutation.
    Iannaccone A, Mura M, Dyka FM, Ciccarelli ML, Yashar BM, Ayyagari R, Jablonski MM, Molday RS.
    Vision Res; 2006 Oct; 46(22):3845-52. PubMed ID: 16884758
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  • 15. Clinical characteristics of 14 japanese patients with X-linked juvenile retinoschisis associated with XLRS1 mutation.
    Shinoda K, Ishida S, Oguchi Y, Mashima Y.
    Ophthalmic Genet; 2000 Sep; 21(3):171-80. PubMed ID: 11035549
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  • 16. Novel mutations in the arrestin gene and associated clinical features in Japanese patients with Oguchi's disease.
    Nakamura M, Yamamoto S, Okada M, Ito S, Tano Y, Miyake Y.
    Ophthalmology; 2004 Jul; 111(7):1410-4. PubMed ID: 15234147
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  • 17. DNA analysis for diagnosis of x-linked juvenile retinoschisis when clinical examination is difficult in a young child.
    Kawano T, Sato M, Hikoya A, Nishimura K, Hotta Y.
    Jpn J Ophthalmol; 2005 Jul; 49(3):268-70. PubMed ID: 15944839
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  • 18. Abnormal cone structure in foveal schisis cavities in X-linked retinoschisis from mutations in exon 6 of the RS1 gene.
    Duncan JL, Ratnam K, Birch DG, Sundquist SM, Lucero AS, Zhang Y, Meltzer M, Smaoui N, Roorda A.
    Invest Ophthalmol Vis Sci; 2011 Dec 20; 52(13):9614-23. PubMed ID: 22110067
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  • 19. A novel gene mutation in a family with X-linked retinoschisis.
    Lai YH, Huang SP, Chen SP, Hu PS, Lin SF, Sheu MM, Wang HZ, Tsai RK.
    J Formos Med Assoc; 2015 Sep 20; 114(9):872-80. PubMed ID: 24529551
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  • 20. Genotypic and phenotypic spectrum of X-linked retinoschisis in Australia.
    Hewitt AW, FitzGerald LM, Scotter LW, Mulhall LE, McKay JD, Mackey DA.
    Clin Exp Ophthalmol; 2005 Jun 20; 33(3):233-9. PubMed ID: 15932525
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