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11. Visual rehabilitation of patients with Stargardt's disease. Shah M; Zaman M; Khan MT; Khan MD J Coll Physicians Surg Pak; 2008 May; 18(5):294-8. PubMed ID: 18541085 [TBL] [Abstract][Full Text] [Related]
12. Stargardt's type macular dystrophy associated with retinitis pigmentosa. Charney RE; Kraushar MF; Appel N Ann Ophthalmol; 1982 Feb; 14(2):118-9. PubMed ID: 7092020 [TBL] [Abstract][Full Text] [Related]
13. Isotretinoin treatment inhibits lipofuscin accumulation in a mouse model of recessive Stargardt's macular degeneration. Radu RA; Mata NL; Nusinowitz S; Liu X; Travis GH Novartis Found Symp; 2004; 255():51-63; discussion 63-7, 177-8. PubMed ID: 14750596 [TBL] [Abstract][Full Text] [Related]
14. Comparison of visual acuity loss in patients with different stages of Stargardt's disease. Kim LS; Fishman GA Ophthalmology; 2006 Oct; 113(10):1748-51. PubMed ID: 16872677 [TBL] [Abstract][Full Text] [Related]
16. Initial rapid decrease in visual acuity in siblings with Stargardt's disease. Hayasaka S; Kurome H; Noda S; Mihara M Jpn J Ophthalmol; 1993; 37(4):485-9. PubMed ID: 8145394 [TBL] [Abstract][Full Text] [Related]
17. Assessment of central visual function in Stargardt's disease/fundus flavimaculatus with ultrahigh-resolution optical coherence tomography. Ergun E; Hermann B; Wirtitsch M; Unterhuber A; Ko TH; Sattmann H; Scholda C; Fujimoto JG; Stur M; Drexler W Invest Ophthalmol Vis Sci; 2005 Jan; 46(1):310-6. PubMed ID: 15623790 [TBL] [Abstract][Full Text] [Related]
18. [Macular and multifocal electroretinography in the diagnosis of Stargardt's dystrophy]. Zol'nikova IV; Karlova IZ; Rogatina EV Vestn Oftalmol; 2009; 125(1):41-6. PubMed ID: 19284101 [TBL] [Abstract][Full Text] [Related]
19. Stargardt's disease is not allelic to the genes for neuronal ceroid lipofuscinoses. Gerber S; Odent S; Postel-Vinay A; Janin N; Dufier JL; Munnich A; Frezal J; Kaplan J J Med Genet; 1994 Mar; 31(3):222-3. PubMed ID: 8014971 [TBL] [Abstract][Full Text] [Related]
20. Retinal astrocytic hamartoma and Stargardt's disease: unusual association in a patient with ABCR mutation without phacomatosis. Bini A; Sodi A; Passerini I; Menchini U; Torricelli F Clin Exp Ophthalmol; 2007 Nov; 35(8):777-9. PubMed ID: 17997789 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]