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4. Lens-sparing vitrectomy effective for reattachment of newly developed falciform retinal detachment in a patient with Norrie disease. Shima C; Kusaka S; Kondo H; Hasebe H; Fujikado T; Tano Y Arch Ophthalmol; 2009 Apr; 127(4):579-80. PubMed ID: 19365046 [No Abstract] [Full Text] [Related]
5. Genotype-phenotype variations in five Spanish families with Norrie disease or X-linked FEVR. Riveiro-Alvarez R; Trujillo-Tiebas MJ; Gimenez-Pardo A; Garcia-Hoyos M; Cantalapiedra D; Lorda-Sanchez I; Rodriguez de Alba M; Ramos C; Ayuso C Mol Vis; 2005 Sep; 11():705-12. PubMed ID: 16163268 [TBL] [Abstract][Full Text] [Related]
6. Repair of Total Tractional Retinal Detachment in Norrie Disease: Report of Technique and Successful Surgical Outcome. Todorich B; Thanos A; Yonekawa Y; Capone A Ophthalmic Surg Lasers Imaging Retina; 2017 Mar; 48(3):260-262. PubMed ID: 28297040 [TBL] [Abstract][Full Text] [Related]
7. Retinal phenotype-genotype correlation of pediatric patients expressing mutations in the Norrie disease gene. Wu WC; Drenser K; Trese M; Capone A; Dailey W Arch Ophthalmol; 2007 Feb; 125(2):225-30. PubMed ID: 17296899 [TBL] [Abstract][Full Text] [Related]
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9. A novel contiguous deletion involving NDP, MAOB and EFHC2 gene in a patient with familial Norrie disease: bilateral blindness and leucocoria without other deficits. Jia B; Huang L; Chen Y; Liu S; Chen C; Xiong K; Song L; Zhou Y; Yang X; Zhong M J Genet; 2017 Dec; 96(6):1015-1020. PubMed ID: 29321361 [TBL] [Abstract][Full Text] [Related]
10. Pars plana lensectomy and intraocular lens implantation in pediatric radiation-induced cataracts in retinoblastoma. Miller DM; Murray TG; Cicciarelli NL; Capo H; Markoe AM Ophthalmology; 2005 Sep; 112(9):1620-4. PubMed ID: 16024083 [TBL] [Abstract][Full Text] [Related]
11. Advanced bilateral persistent fetal vasculature associated with a novel mutation in the Norrie gene. Dhingra S; Shears DJ; Blake V; Stewart H; Patel CK Br J Ophthalmol; 2006 Oct; 90(10):1324-5. PubMed ID: 16980647 [No Abstract] [Full Text] [Related]
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15. A novel missense NDP mutation [p.(Cys93Arg)] with a manifesting carrier in an austrian family with Norrie disease. Parzefall T; Lucas T; Ritter M; Ludwig M; Ramsebner R; Frohne A; Schöfer C; Hengstschläger M; Frei K Audiol Neurootol; 2014; 19(3):203-9. PubMed ID: 24801666 [TBL] [Abstract][Full Text] [Related]
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