177 related articles for article (PubMed ID: 16521245)
21. 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; 144(3):419-423. PubMed ID: 17631851
[TBL] [Abstract][Full Text] [Related]
22. [Detection and prenatal diagnosis for RS1 gene mutations in two Chinese families with X-linked juvenile retinoschisis].
Chu Y; Fang D; Hou QF; Wang LY; Guo XR; Wang YT; Liao SX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Apr; 30(2):199-202. PubMed ID: 23568735
[TBL] [Abstract][Full Text] [Related]
23. The genetic spectrum and clinical features of X-linked juvenile retinoschisis in Central China.
Liu Z; Guo J; Pan M; Xie K; Du L; Jin X; Lei B
Ophthalmic Genet; 2023 Jun; 44(3):262-270. PubMed ID: 36856325
[TBL] [Abstract][Full Text] [Related]
24. Correlation of genetic and clinical findings in Spanish patients with X-linked juvenile retinoschisis.
Riveiro-Alvarez R; Trujillo-Tiebas MJ; Gimenez-Pardo A; Garcia-Hoyos M; Lopez-Martinez MA; Aguirre-Lamban J; Garcia-Sandoval B; Vazquez-Fernandez del Pozo S; Cantalapiedra D; Avila-Fernandez A; Baiget M; Ramos C; Ayuso C
Invest Ophthalmol Vis Sci; 2009 Sep; 50(9):4342-50. PubMed ID: 19324861
[TBL] [Abstract][Full Text] [Related]
25. Multimodal imaging in a pedigree of X-linked Retinoschisis with a novel RS1 variant.
Stephenson K; Dockery A; Wynne N; Carrigan M; Kenna P; Jane Farrar G; Keegan D
BMC Med Genet; 2018 Nov; 19(1):195. PubMed ID: 30419843
[TBL] [Abstract][Full Text] [Related]
26. X-linked retinoschisis in a female with a heterozygous RS1 missense mutation.
Saldana M; Thompson J; Monk E; Trump D; Long V; Sheridan E
Am J Med Genet A; 2007 Mar; 143A(6):608-9. PubMed ID: 17304551
[No Abstract] [Full Text] [Related]
27. Gene symbol: CRB1.
Vallespin E; Millan JM; Riveiro-Alvarez R; Aguirre-Lamban J; Cantalapiedra D; Gallego J; Trujillo-Tiebas MJ; Ayuso C
Hum Genet; 2007 Feb; 120(6):914. PubMed ID: 17438615
[No Abstract] [Full Text] [Related]
28. 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
[TBL] [Abstract][Full Text] [Related]
29. R213W mutation in the retinoschisis 1 gene causes X-linked juvenile retinoschisis in a large Chinese family.
Xu J; Gu H; Ma K; Liu X; Snellingen T; Sun E; Wang N; Liu N
Mol Vis; 2010 Aug; 16():1593-600. PubMed ID: 20806044
[TBL] [Abstract][Full Text] [Related]
30. Mutation analysis of the VMD2 gene in thai families with best macular dystrophy.
Atchaneeyasakul LO; Jinda W; Sakolsatayadorn N; Trinavarat A; Ruangvoravate N; Thanasombatskul N; Thongnoppakhun W; Limwongse C
Ophthalmic Genet; 2008 Sep; 29(3):139-44. PubMed ID: 18766995
[TBL] [Abstract][Full Text] [Related]
31. X-Linked Retinoschisis without Macular Retinoschisis: A New RS1 Mutation.
Alfonso-Muñoz EA; Català-Mora J; Díaz-Cascajosa J
Ophthalmol Retina; 2020 Jul; 4(7):719. PubMed ID: 32646553
[No Abstract] [Full Text] [Related]
32. Prolonged recovery of retinal structure/function after gene therapy in an Rs1h-deficient mouse model of x-linked juvenile retinoschisis.
Min SH; Molday LL; Seeliger MW; Dinculescu A; Timmers AM; Janssen A; Tonagel F; Tanimoto N; Weber BH; Molday RS; Hauswirth WW
Mol Ther; 2005 Oct; 12(4):644-51. PubMed ID: 16027044
[TBL] [Abstract][Full Text] [Related]
33. X-linked juvenile retinoschisis (XLRS): a review of genotype-phenotype relationships.
Kim DY; Mukai S
Semin Ophthalmol; 2013; 28(5-6):392-6. PubMed ID: 24138048
[TBL] [Abstract][Full Text] [Related]
34. Novel mutation in BEST1 associated with retinoschisis.
Silva RA; Berrocal AM; Lam BL; Albini TA
JAMA Ophthalmol; 2013 Jun; 131(6):794-8. PubMed ID: 23572118
[No Abstract] [Full Text] [Related]
35. Genotypic analysis of X-linked retinoschisis in Western Australia.
Lamey T; Laurin S; Chelva E; De Roach J
Adv Exp Med Biol; 2010; 664():283-91. PubMed ID: 20238027
[TBL] [Abstract][Full Text] [Related]
36. 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; 123(1):21-7. PubMed ID: 21701876
[TBL] [Abstract][Full Text] [Related]
37. 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
[TBL] [Abstract][Full Text] [Related]
38. Gene symbol: FAH. Disease: tyrosinaemia 1.
Arranz A; Rigante D; Antuzzi D; Riudor E
Hum Genet; 2005 Dec; 118(3-4):537. PubMed ID: 16521249
[No Abstract] [Full Text] [Related]
39. 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; 43(7):643-7. PubMed ID: 25894957
[TBL] [Abstract][Full Text] [Related]
40. Gene symbol: mc4r. Disease: obesity.
Jia WP
Hum Genet; 2005 Dec; 118(3-4):548. PubMed ID: 16521308
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]