These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

260 related items for PubMed ID: 26043410

  • 1. The gene mutation in a Taiwanese family with X-linked retinoschisis.
    Huang CT, Chen SP, Tsai RK.
    Kaohsiung J Med Sci; 2015 Jun; 31(6):309-14. PubMed ID: 26043410
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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 Sep; 14():2321-32. PubMed ID: 19093009
    [Abstract] [Full Text] [Related]

  • 4. 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; 26(3):111-7. PubMed ID: 16272055
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. 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; 33(3):233-9. PubMed ID: 15932525
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Truncation of retinoschisin protein associated with a novel splice site mutation in the RS1 gene.
    Lesch B, Szabó V, Kánya M, Varsányi B, Somfai GM, Hargitai J, Vámos R, Fiedler O, Farkas A.
    Mol Vis; 2008 Aug 25; 14():1549-58. PubMed ID: 18728755
    [Abstract] [Full Text] [Related]

  • 9. 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 25; 120(7):1454-64. PubMed ID: 23453514
    [Abstract] [Full Text] [Related]

  • 10. 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 25; 144(3):419-423. PubMed ID: 17631851
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. 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 25; 50(11):5375-83. PubMed ID: 19474399
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Comprehensive analysis of genetic and clinical characteristics of 30 patients with X-linked juvenile retinoschisis in China.
    Gao FJ, Dong JH, Wang DD, Chen F, Hu FY, Chang Q, Xu P, Liu W, Li JK, Huang Y, Wu JH, Xu GZ.
    Acta Ophthalmol; 2021 Jun 07; 99(4):e470-e479. PubMed ID: 33124204
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Clinical and molecular characterization of females affected by X-linked retinoschisis.
    Staffieri SE, Rose L, Chang A, De Roach JN, McLaren TL, Mackey DA, Hewitt AW, Lamey TM.
    Clin Exp Ophthalmol; 2015 Jun 07; 43(7):643-7. PubMed ID: 25894957
    [Abstract] [Full Text] [Related]

  • 19. Genotypic and phenotypic diversity in X-linked retinoschisis: Findings from a South Indian patient cohort.
    Chowdhury S, Chermakani P, Baliga G, Anjanamurthy R, Sundaresan P.
    Indian J Ophthalmol; 2024 Jun 01; 72(6):902-911. PubMed ID: 38317323
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.