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.
439 related articles for article (PubMed ID: 21071739)
21. The effect of peripherin/rds haploinsufficiency on rod and cone photoreceptors. Cheng T; Peachey NS; Li S; Goto Y; Cao Y; Naash MI J Neurosci; 1997 Nov; 17(21):8118-28. PubMed ID: 9334387 [TBL] [Abstract][Full Text] [Related]
22. Macular appearance by means of OCT and electrophysiology in members of two families with different mutations in RDS (the peripherin/RDS gene). Schatz P; Abrahamson M; Eksandh L; Ponjavic V; Andréasson S Acta Ophthalmol Scand; 2003 Oct; 81(5):500-7. PubMed ID: 14510799 [TBL] [Abstract][Full Text] [Related]
23. Modulating expression of peripherin/rds in transgenic mice: critical levels and the effect of overexpression. Nour M; Ding XQ; Stricker H; Fliesler SJ; Naash MI Invest Ophthalmol Vis Sci; 2004 Aug; 45(8):2514-21. PubMed ID: 15277471 [TBL] [Abstract][Full Text] [Related]
25. Macular dystrophy associated with the Arg172Trp substitution in peripherin/RDS: genotype-phenotype correlation. Anand S; Sheridan E; Cassidy F; Inglehearn C; Williams G; Springell K; Allgar V; Kelly TL; McKibbin M Retina; 2009 May; 29(5):682-8. PubMed ID: 19262438 [TBL] [Abstract][Full Text] [Related]
26. Phenotypic variation including retinitis pigmentosa, pattern dystrophy, and fundus flavimaculatus in a single family with a deletion of codon 153 or 154 of the peripherin/RDS gene. Weleber RG; Carr RE; Murphey WH; Sheffield VC; Stone EM Arch Ophthalmol; 1993 Nov; 111(11):1531-42. PubMed ID: 8240110 [TBL] [Abstract][Full Text] [Related]
27. Mutations and polymorphisms in the human peripherin-RDS gene and their involvement in inherited retinal degeneration. Keen TJ; Inglehearn CF Hum Mutat; 1996; 8(4):297-303. PubMed ID: 8956033 [TBL] [Abstract][Full Text] [Related]
28. Atypical presentation of pattern dystrophy in two families with peripherin/RDS mutations. Grover S; Fishman GA; Stone EM Ophthalmology; 2002 Jun; 109(6):1110-7. PubMed ID: 12045052 [TBL] [Abstract][Full Text] [Related]
30. Pattern dystrophy with high intrafamilial variability associated with Y141C mutation in the peripherin/RDS gene and successful treatment of subfoveal CNV related to multifocal pattern type with anti-VEGF (ranibizumab) intravitreal injections. Vaclavik V; Tran HV; Gaillard MC; Schorderet DF; Munier FL Retina; 2012 Oct; 32(9):1942-9. PubMed ID: 22466463 [TBL] [Abstract][Full Text] [Related]
31. Phenotypic variability and long-term follow-up of patients with known and novel PRPH2/RDS gene mutations. Renner AB; Fiebig BS; Weber BH; Wissinger B; Andreasson S; Gal A; Cropp E; Kohl S; Kellner U Am J Ophthalmol; 2009 Mar; 147(3):518-530.e1. PubMed ID: 19038374 [TBL] [Abstract][Full Text] [Related]
32. Genetic heterogeneity of butterfly-shaped pigment dystrophy of the fovea. van Lith-Verhoeven JJ; Cremers FP; van den Helm B; Hoyng CB; Deutman AF Mol Vis; 2003 Apr; 9():138-43. PubMed ID: 12724643 [TBL] [Abstract][Full Text] [Related]
33. A Swedish family with a mutation in the peripherin/RDS gene (Arg-172-Trp) associated with a progressive retinal degeneration. Ekström U; Andréasson S; Ponjavic V; Abrahamson M; Sandgren O; Nilsson-Ehle P; Ehinger B Ophthalmic Genet; 1998 Sep; 19(3):149-56. PubMed ID: 9810570 [TBL] [Abstract][Full Text] [Related]
34. Clinical findings in a multigeneration family with autosomal dominant central areolar choroidal dystrophy associated with an Arg195Leu mutation in the peripherin/RDS gene. Keilhauer CN; Meigen T; Weber BH Arch Ophthalmol; 2006 Jul; 124(7):1020-7. PubMed ID: 16832026 [TBL] [Abstract][Full Text] [Related]
35. High prevalence of mutations in peripherin/RDS in autosomal dominant macular dystrophies in a Spanish population. Gamundi MJ; Hernan I; Muntanyola M; Trujillo MJ; García-Sandoval B; Ayuso C; Baiget M; Carballo M Mol Vis; 2007 Jun; 13():1031-7. PubMed ID: 17653047 [TBL] [Abstract][Full Text] [Related]
36. High-resolution in vivo imaging of the RPE mosaic in eyes with retinal disease. Roorda A; Zhang Y; Duncan JL Invest Ophthalmol Vis Sci; 2007 May; 48(5):2297-303. PubMed ID: 17460294 [TBL] [Abstract][Full Text] [Related]
37. Phenotypic expression of autosomal dominant retinitis pigmentosa in a Swedish family expressing a Phe-211-Leu variant of peripherin/RDS. Ekström U; Ponjavic V; Abrahamson M; Nilsson-Ehle P; Andrëasson S; Stenström I; Ehinger B Ophthalmic Genet; 1998 Mar; 19(1):27-37. PubMed ID: 9587927 [TBL] [Abstract][Full Text] [Related]
38. Nonallelism of erd and prcd and exclusion of the canine RDS/peripherin gene as a candidate for both retinal degeneration loci. Ray K; Acland GM; Aguirre GD Invest Ophthalmol Vis Sci; 1996 Apr; 37(5):783-94. PubMed ID: 8603863 [TBL] [Abstract][Full Text] [Related]
39. Morphologic characteristics of the outer retina in cone dystrophy on spectral-domain optical coherence tomography. Cho SC; Woo SJ; Park KH; Hwang JM Korean J Ophthalmol; 2013 Feb; 27(1):19-27. PubMed ID: 23372375 [TBL] [Abstract][Full Text] [Related]
40. A point mutation in the RDS-peripherin gene in a Spanish family with central areolar choroidal dystrophy. Reig C; Serra A; Gean E; Vidal M; Arumí J; De la Calzada MD; Antich J; Carballo M Ophthalmic Genet; 1995 Jun; 16(2):39-44. PubMed ID: 7493155 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]