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383 related items for PubMed ID: 16272055
1. 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]
2. RS-1 Gene Delivery to an Adult Rs1h Knockout Mouse Model Restores ERG b-Wave with Reversal of the Electronegative Waveform of X-Linked Retinoschisis. Zeng Y, Takada Y, Kjellstrom S, Hiriyanna K, Tanikawa A, Wawrousek E, Smaoui N, Caruso R, Bush RA, Sieving PA. Invest Ophthalmol Vis Sci; 2004 Sep; 45(9):3279-85. PubMed ID: 15326152 [Abstract] [Full Text] [Related]
3. 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 [Abstract] [Full Text] [Related]
4. 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; 120(7):1454-64. PubMed ID: 23453514 [Abstract] [Full Text] [Related]
5. 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]
6. 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 20; 144(3):419-423. PubMed ID: 17631851 [Abstract] [Full Text] [Related]
7. 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 20; 14():2321-32. PubMed ID: 19093009 [Abstract] [Full Text] [Related]
8. 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 [Abstract] [Full Text] [Related]
9. Optical coherence tomography in the diagnosis of juvenile X-linked retinoschisis. Eriksson U, Larsson E, Holmström G. Acta Ophthalmol Scand; 2004 Apr 20; 82(2):218-23. PubMed ID: 15043546 [Abstract] [Full Text] [Related]
10. 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 20; 50(11):5375-83. PubMed ID: 19474399 [Abstract] [Full Text] [Related]
11. ERG variability in X-linked congenital retinoschisis patients with mutations in the RS1 gene and the diagnostic importance of fundus autofluorescence and OCT. Renner AB, Kellner U, Fiebig B, Cropp E, Foerster MH, Weber BH. Doc Ophthalmol; 2008 Mar 20; 116(2):97-109. PubMed ID: 17987333 [Abstract] [Full Text] [Related]
12. 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]
14. 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 25; 21(3):171-80. PubMed ID: 11035549 [Abstract] [Full Text] [Related]
15. 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 25; 112(12):2115. PubMed ID: 16225923 [Abstract] [Full Text] [Related]
16. Retinal Function in X-Linked Juvenile Retinoschisis. Ambrosio L, Hansen RM, Kimia R, Fulton AB. Invest Ophthalmol Vis Sci; 2019 Nov 01; 60(14):4872-4881. PubMed ID: 31747688 [Abstract] [Full Text] [Related]
17. The gene mutation in a Taiwanese family with X-linked retinoschisis. Huang CT, Chen SP, Tsai RK. Kaohsiung J Med Sci; 2015 Jun 01; 31(6):309-14. PubMed ID: 26043410 [Abstract] [Full Text] [Related]
18. Phenotypic characterization of X-linked retinoschisis: Clinical, electroretinography, and optical coherence tomography variables. Neriyanuri S, Dhandayuthapani S, Arunachalam JP, Raman R. Indian J Ophthalmol; 2016 Jul 01; 64(7):513-7. PubMed ID: 27609164 [Abstract] [Full Text] [Related]
19. Macular dysfunction and morphology in spinocerebellar ataxia type 7 (SCA 7). Hugosson T, Gränse L, Ponjavic V, Andréasson S. Ophthalmic Genet; 2009 Mar 01; 30(1):1-6. PubMed ID: 19172503 [Abstract] [Full Text] [Related]
20. 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 Mar 01; 21():487-501. PubMed ID: 25999676 [Abstract] [Full Text] [Related] Page: [Next] [New Search]