318 related articles for article (PubMed ID: 28235399)
1. Case report of an atypical early onset X-linked retinoschisis in monozygotic twins.
Murro V; Caputo R; Bacci GM; Sodi A; Mucciolo DP; Bargiacchi S; Giglio SR; Virgili G; Rizzo S
BMC Ophthalmol; 2017 Feb; 17(1):19. PubMed ID: 28235399
[TBL] [Abstract][Full Text] [Related]
2. 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; 64(7):513-7. PubMed ID: 27609164
[TBL] [Abstract][Full Text] [Related]
3. 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
[TBL] [Abstract][Full Text] [Related]
4. 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; 99(4):e470-e479. PubMed ID: 33124204
[TBL] [Abstract][Full Text] [Related]
5. 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
[TBL] [Abstract][Full Text] [Related]
6. 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
[TBL] [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; 14():2321-32. PubMed ID: 19093009
[TBL] [Abstract][Full Text] [Related]
8. X-linked juvenile retinoschisis in a consanguineous family: phenotypic variability and report of a homozygous female patient.
Gliem M; Holz FG; Stöhr H; Weber BH; Charbel Issa P
Retina; 2014 Dec; 34(12):2472-8. PubMed ID: 25054456
[TBL] [Abstract][Full Text] [Related]
9. Of men and mice: Human X-linked retinoschisis and fidelity in mouse modeling.
Vijayasarathy C; Sardar Pasha SPB; Sieving PA
Prog Retin Eye Res; 2022 Mar; 87():100999. PubMed ID: 34390869
[TBL] [Abstract][Full Text] [Related]
10. Phenotypic Characteristics of a French Cohort of Patients with X-Linked Retinoschisis.
Orès R; Mohand-Said S; Dhaenens CM; Antonio A; Zeitz C; Augstburger E; Andrieu C; Sahel JA; Audo I
Ophthalmology; 2018 Oct; 125(10):1587-1596. PubMed ID: 29739629
[TBL] [Abstract][Full Text] [Related]
11. Peripheral fundus findings in X-linked retinoschisis.
Fahim AT; Ali N; Blachley T; Michaelides M
Br J Ophthalmol; 2017 Nov; 101(11):1555-1559. PubMed ID: 28348004
[TBL] [Abstract][Full Text] [Related]
12. 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
[TBL] [Abstract][Full Text] [Related]
13. 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
[TBL] [Abstract][Full Text] [Related]
14. 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; 21():487-501. PubMed ID: 25999676
[TBL] [Abstract][Full Text] [Related]
15. 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; 52(13):9614-23. PubMed ID: 22110067
[TBL] [Abstract][Full Text] [Related]
16. Preclinical Dose-Escalation Study of Intravitreal AAV-RS1 Gene Therapy in a Mouse Model of X-linked Retinoschisis: Dose-Dependent Expression and Improved Retinal Structure and Function.
Bush RA; Zeng Y; Colosi P; Kjellstrom S; Hiriyanna S; Vijayasarathy C; Santos M; Li J; Wu Z; Sieving PA
Hum Gene Ther; 2016 May; 27(5):376-89. PubMed ID: 27036983
[TBL] [Abstract][Full Text] [Related]
17. Effect of light and diurnal variation on macular thickness in X-linked retinoschisis: a case series.
Rubinstein Y; Weiner C; Chetrit N; Newman H; Hecht I; Shoshany N; Pras E
Graefes Arch Clin Exp Ophthalmol; 2020 Mar; 258(3):529-536. PubMed ID: 31897705
[TBL] [Abstract][Full Text] [Related]
18. X-Linked Retinoschisis: Novel Clinical Observations and Genetic Spectrum in 340 Patients.
Hahn LC; van Schooneveld MJ; Wesseling NL; Florijn RJ; Ten Brink JB; Lissenberg-Witte BI; Strubbe I; Meester-Smoor MA; Thiadens AA; Diederen RM; van Cauwenbergh C; de Zaeytijd J; Walraedt S; de Baere E; Klaver CCW; Ossewaarde-van Norel J; van den Born LI; Hoyng CB; van Genderen MM; Sieving PA; Leroy BP; Bergen AA; Boon CJF
Ophthalmology; 2022 Feb; 129(2):191-202. PubMed ID: 34624300
[TBL] [Abstract][Full Text] [Related]
19. 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
[TBL] [Abstract][Full Text] [Related]
20. 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; 72(6):902-911. PubMed ID: 38317323
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
