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.
269 related articles for article (PubMed ID: 27258436)
1. Biallelic Mutations in CRB1 Underlie Autosomal Recessive Familial Foveal Retinoschisis. Vincent A; Ng J; Gerth-Kahlert C; Tavares E; Maynes JT; Wright T; Tiwari A; Tumber A; Li S; Hanson JV; Bahr A; MacDonald H; Bähr L; Westall C; Berger W; Cremers FP; den Hollander AI; Héon E Invest Ophthalmol Vis Sci; 2016 May; 57(6):2637-46. PubMed ID: 27258436 [TBL] [Abstract][Full Text] [Related]
2. Whole exome sequencing identifies CRB1 defect in an unusual maculopathy phenotype. Tsang SH; Burke T; Oll M; Yzer S; Lee W; Xie YA; Allikmets R Ophthalmology; 2014 Sep; 121(9):1773-82. PubMed ID: 24811962 [TBL] [Abstract][Full Text] [Related]
3. Clinical and Genetic Analysis of 63 Families Demonstrating Early and Advanced Characteristic Fundus as the Signature of CRB1 Mutations. Wang Y; Sun W; Xiao X; Li S; Jia X; Wang P; Zhang Q Am J Ophthalmol; 2021 Mar; 223():160-168. PubMed ID: 33342761 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. Clinical and genetic characteristics of Leber congenital amaurosis with novel mutations in known genes based on a Chinese eastern coast Han population. Wang S; Zhang Q; Zhang X; Wang Z; Zhao P Graefes Arch Clin Exp Ophthalmol; 2016 Nov; 254(11):2227-2238. PubMed ID: 27422788 [TBL] [Abstract][Full Text] [Related]
6. 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. Autosomal recessive bestrophinopathy: differential diagnosis and treatment options. Boon CJ; van den Born LI; Visser L; Keunen JE; Bergen AA; Booij JC; Riemslag FC; Florijn RJ; van Schooneveld MJ Ophthalmology; 2013 Apr; 120(4):809-20. PubMed ID: 23290749 [TBL] [Abstract][Full Text] [Related]
9. Identification of a novel CRB1 variant in a compound heterozygous state in a patient with CRB1-associated maculopathy and foveal retinoschisis. Cheng Z; Hagan R; Yeo DCM Ophthalmic Genet; 2022 Apr; 43(2):253-257. PubMed ID: 34783605 [TBL] [Abstract][Full Text] [Related]
10. Phenotypic features of CRB1-associated early-onset severe retinal dystrophy and the different molecular approaches to identifying the disease-causing variants. Kousal B; Dudakova L; Gaillyova R; Hejtmankova M; Diblik P; Michaelides M; Liskova P Graefes Arch Clin Exp Ophthalmol; 2016 Sep; 254(9):1833-9. PubMed ID: 27113771 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Benign Yellow Dot Maculopathy: A New Macular Phenotype. Dev Borman A; Rachitskaya A; Suzani M; Sisk RA; Ahmed ZM; Holder GE; Cipriani V; Arno G; Webster AR; Hufnagel RB; Berrocal A; Moore AT Ophthalmology; 2017 Jul; 124(7):1004-1013. PubMed ID: 28366503 [TBL] [Abstract][Full Text] [Related]
13. Overlapping retinal phenotypes in a consanguineous family harboring mutations in CRB1 and RS1. Khan AO; El-Ghrably IA Ophthalmic Genet; 2019 Feb; 40(1):17-21. PubMed ID: 30608181 [TBL] [Abstract][Full Text] [Related]
14. Long-term follow-up of a CRB1-associated maculopathy. Mucciolo DP; Murro V; Giorgio D; Passerini I; Sodi A; Virgili G; Rizzo S Ophthalmic Genet; 2018 Aug; 39(4):522-525. PubMed ID: 29869924 [TBL] [Abstract][Full Text] [Related]
15. Posterior microphthalmos, retinitis pigmentosa, and foveoschisis caused by a mutation in the Morillo Sánchez MJ; Llavero Valero P; González-Del Pozo M; Ponte Zuñiga B; Antiñolo G; Ramos Jiménez M; Rodríguez De La Rúa Franch E Ophthalmic Genet; 2019 Jun; 40(3):288-292. PubMed ID: 31264930 [No Abstract] [Full Text] [Related]
16. Parafoveal Photoreceptor Abnormalities in Asymptomatic Patients With RP1L1 Mutations in Families With Occult Macular Dystrophy. Kato Y; Hanazono G; Fujinami K; Hatase T; Kawamura Y; Iwata T; Miyake Y; Tsunoda K Invest Ophthalmol Vis Sci; 2017 Dec; 58(14):6020-6029. PubMed ID: 29196766 [TBL] [Abstract][Full Text] [Related]
17. Foveal cavitation as an optical coherence tomography finding in central cone dysfunction. Leng T; Marmor MF; Kellner U; Thompson DA; Renner AB; Moore W; Sowden JC Retina; 2012 Jul; 32(7):1411-9. PubMed ID: 22466470 [TBL] [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; 64(7):513-7. PubMed ID: 27609164 [TBL] [Abstract][Full Text] [Related]
19. 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]
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]