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Journal Abstract Search
1211 related items for PubMed ID: 17591900
1. High-resolution imaging with adaptive optics in patients with inherited retinal degeneration. Duncan JL, Zhang Y, Gandhi J, Nakanishi C, Othman M, Branham KE, Swaroop A, Roorda A. Invest Ophthalmol Vis Sci; 2007 Jul; 48(7):3283-91. PubMed ID: 17591900 [Abstract] [Full Text] [Related]
3. Multifocal ERG reveals several patterns of cone degeneration in retinitis pigmentosa with concentric narrowing of the visual field. Janáky M, Pálffy A, Deák A, Szilágyi M, Benedek G. Invest Ophthalmol Vis Sci; 2007 Jan; 48(1):383-9. PubMed ID: 17197558 [Abstract] [Full Text] [Related]
5. H244R VSX1 is associated with selective cone ON bipolar cell dysfunction and macular degeneration in a PPCD family. Valleix S, Nedelec B, Rigaudiere F, Dighiero P, Pouliquen Y, Renard G, Le Gargasson JF, Delpech M. Invest Ophthalmol Vis Sci; 2006 Jan; 47(1):48-54. PubMed ID: 16384943 [Abstract] [Full Text] [Related]
11. Defective cone photoreceptor cytoskeleton, alignment, feedback, and energetics can lead to energy depletion in macular degeneration. Eckmiller MS. Prog Retin Eye Res; 2004 Sep 09; 23(5):495-522. PubMed ID: 15302348 [Abstract] [Full Text] [Related]
12. Screen of the IMPDH1 gene among patients with dominant retinitis pigmentosa and clinical features associated with the most common mutation, Asp226Asn. Wada Y, Sandberg MA, McGee TL, Stillberger MA, Berson EL, Dryja TP. Invest Ophthalmol Vis Sci; 2005 May 09; 46(5):1735-41. PubMed ID: 15851576 [Abstract] [Full Text] [Related]
14. Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunction. Roosing S, van den Born LI, Hoyng CB, Thiadens AA, de Baere E, Collin RW, Koenekoop RK, Leroy BP, van Moll-Ramirez N, Venselaar H, Riemslag FC, Cremers FP, Klaver CC, den Hollander AI. Ophthalmology; 2013 Jun 09; 120(6):1239-46. PubMed ID: 23499059 [Abstract] [Full Text] [Related]
15. High-resolution imaging of the photoreceptor layer in epiretinal membrane using adaptive optics scanning laser ophthalmoscopy. Ooto S, Hangai M, Takayama K, Sakamoto A, Tsujikawa A, Oshima S, Inoue T, Yoshimura N. Ophthalmology; 2011 May 09; 118(5):873-81. PubMed ID: 21074858 [Abstract] [Full Text] [Related]
16. Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1). Berson EL, Grimsby JL, Adams SM, McGee TL, Sweklo E, Pierce EA, Sandberg MA, Dryja TP. Invest Ophthalmol Vis Sci; 2001 Sep 09; 42(10):2217-24. PubMed ID: 11527933 [Abstract] [Full Text] [Related]
17. Multimodal Approach to Monitoring and Investigating Cone Structure and Function in an Inherited Macular Dystrophy. Ziccardi L, Giannini D, Lombardo G, Serrao S, Dell'Omo R, Nicoletti A, Bertelli M, Lombardo M. Am J Ophthalmol; 2015 Aug 09; 160(2):301-312.e6. PubMed ID: 25908487 [Abstract] [Full Text] [Related]
18. Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases. Nishiguchi KM, Sandberg MA, Gorji N, Berson EL, Dryja TP. Hum Mutat; 2005 Mar 09; 25(3):248-58. PubMed ID: 15712225 [Abstract] [Full Text] [Related]