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Journal Abstract Search


248 related items for PubMed ID: 18728755

  • 1.
    ; . PubMed ID:
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  • 2. Clinical and genetic findings in Hungarian patients with X-linked juvenile retinoschisis.
    Lesch B, Szabó V, Kánya M, Somfai GM, Vámos R, Varsányi B, Pámer Z, Knézy K, Salacz G, Janáky M, Ferencz M, Hargitai J, Papp A, Farkas A.
    Mol Vis; 2008; 14():2321-32. PubMed ID: 19093009
    [Abstract] [Full Text] [Related]

  • 3. Four novel RS1 gene mutations in Polish patients with X-linked juvenile retinoschisis.
    Skorczyk A, Krawczyński MR.
    Mol Vis; 2012; 18():3004-12. PubMed ID: 23288992
    [Abstract] [Full Text] [Related]

  • 4. Null retinoschisin-protein expression from an RS1 c354del1-ins18 mutation causing progressive and severe XLRS in a cross-sectional family study.
    Vijayasarathy C, Ziccardi L, Zeng Y, Smaoui N, Caruso RC, Sieving PA.
    Invest Ophthalmol Vis Sci; 2009 Nov; 50(11):5375-83. PubMed ID: 19474399
    [Abstract] [Full Text] [Related]

  • 5. 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; 114(9):872-80. PubMed ID: 24529551
    [Abstract] [Full Text] [Related]

  • 6. Clinical features of X linked juvenile retinoschisis in Chinese families associated with novel mutations in the RS1 gene.
    Li X, Ma X, Tao Y.
    Mol Vis; 2007 Jun 07; 13():804-12. PubMed ID: 17615541
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Long-term 12 year follow-up of X-linked congenital retinoschisis.
    Kjellström S, Vijayasarathy C, Ponjavic V, Sieving PA, Andréasson S.
    Ophthalmic Genet; 2010 Sep 20; 31(3):114-25. PubMed ID: 20569020
    [Abstract] [Full Text] [Related]

  • 9. Juvenile X-linked retinoschisis with normal scotopic b-wave in the electroretinogram at an early stage of the disease.
    Eksandh L, Andréasson S, Abrahamson M.
    Ophthalmic Genet; 2005 Sep 20; 26(3):111-7. PubMed ID: 16272055
    [Abstract] [Full Text] [Related]

  • 10. Novel mutations of the RS1 gene in a cohort of Chinese families with X-linked retinoschisis.
    Chen J, Xu K, Zhang X, Pan Z, Dong B, Li Y.
    Mol Vis; 2014 Sep 20; 20():132-9. PubMed ID: 24505212
    [Abstract] [Full Text] [Related]

  • 11. 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 20; 138(5):788-98. PubMed ID: 15531314
    [Abstract] [Full Text] [Related]

  • 12. Clinical presentations of X-linked retinoschisis in Taiwanese patients confirmed with genetic sequencing.
    Wang NK, Liu L, Chen HM, Tsai S, Chang TC, Tsai TH, Yang CM, Chao AN, Chen KJ, Kao LY, Yeung L, Yeh LK, Hwang YS, Wu WC, Lai CC.
    Mol Vis; 2015 Nov 20; 21():487-501. PubMed ID: 25999676
    [Abstract] [Full Text] [Related]

  • 13.
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  • 14. A phenotype-genotype correlation study of X-linked retinoschisis.
    Vincent A, Robson AG, Neveu MM, Wright GA, Moore AT, Webster AR, Holder GE.
    Ophthalmology; 2013 Jul 20; 120(7):1454-64. PubMed ID: 23453514
    [Abstract] [Full Text] [Related]

  • 15. A novel deletion mutation in RS1 gene caused X-linked juvenile retinoschisis in a Chinese family.
    Huang Y, Mei L, Gui B, Su W, Liang D, Wu L, Pan Q.
    Eye (Lond); 2014 Nov 20; 28(11):1364-9. PubMed ID: 25168411
    [Abstract] [Full Text] [Related]

  • 16. The Road towards Gene Therapy for X-Linked Juvenile Retinoschisis: A Systematic Review of Preclinical Gene Therapy in Cell-Based and Rodent Models of XLRS.
    van der Veen I, Heredero Berzal A, Koster C, Ten Asbroek ALMA, Bergen AA, Boon CJF.
    Int J Mol Sci; 2024 Jan 19; 25(2):. PubMed ID: 38279267
    [Abstract] [Full Text] [Related]

  • 17. Characterization of novel RS1 exonic deletions in juvenile X-linked retinoschisis.
    D'Souza L, Cukras C, Antolik C, Craig C, Lee JY, He H, Li S, Smaoui N, Hejtmancik JF, Sieving PA, Wang X.
    Mol Vis; 2013 Jan 19; 19():2209-16. PubMed ID: 24227916
    [Abstract] [Full Text] [Related]

  • 18. 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 19; 32(4):429-32. PubMed ID: 15281981
    [Abstract] [Full Text] [Related]

  • 19. Phenotypic expression of X-linked retinoschisis in Chinese families with mutations in the RS1 gene.
    Xu F, Xiang H, Jiang R, Dong F, Sui R.
    Doc Ophthalmol; 2011 Aug 19; 123(1):21-7. PubMed ID: 21701876
    [Abstract] [Full Text] [Related]

  • 20. Genetic studies in a patient with X-linked retinoschisis coexisting with developmental delay and sensorineural hearing loss.
    Sudha D, Patric IRP, Ganapathy A, Agarwal S, Krishna S, Neriyanuri S, Sripriya S, Sen P, Chidambaram S, Arunachalam JP.
    Ophthalmic Genet; 2017 Aug 19; 38(3):260-266. PubMed ID: 28574807
    [Abstract] [Full Text] [Related]


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