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Journal Abstract Search

102 related items for PubMed ID: 77352

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  • 5. Novel NR2E3 mutations (R104Q, R334G) associated with a mild form of enhanced S-cone syndrome demonstrate compound heterozygosity.
    Hayashi T, Gekka T, Goto-Omoto S, Takeuchi T, Kubo A, Kitahara K.
    Ophthalmology; 2005 Dec; 112(12):2115. PubMed ID: 16225923
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  • 8. [Juvenile macular degenerations].
    François J.
    Arch Ophtalmol Rev Gen Ophtalmol; 1974 Dec; 34(6-7):497-512. PubMed ID: 4142583
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  • 12. High-resolution retinal imaging of cone-rod dystrophy.
    Wolfing JI, Chung M, Carroll J, Roorda A, Williams DR.
    Ophthalmology; 2006 Jun; 113(6):1019.e1. PubMed ID: 16650474
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  • 14. Autosomal dominant macular atrophy at 6q14 excludes CORD7 and MCDR1/PBCRA loci.
    Griesinger IB, Sieving PA, Ayyagari R.
    Invest Ophthalmol Vis Sci; 2000 Jan; 41(1):248-55. PubMed ID: 10634627
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  • 18. Morphological study of acute zonal occult outer retinopathy (AZOOR) by multiplanar optical coherence tomography.
    Takai Y, Ishiko S, Kagokawa H, Fukui K, Takahashi A, Yoshida A.
    Acta Ophthalmol; 2009 Jun; 87(4):408-18. PubMed ID: 18778338
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  • 19. Concentric retinitis pigmentosa: clinicopathologic correlations.
    Milam AH, De Castro EB, Smith JE, Tang WX, John SK, Gorin MB, Stone EM, Aguirre GD, Jacobson SG.
    Exp Eye Res; 2001 Oct; 73(4):493-508. PubMed ID: 11825021
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  • 20. Sveinsson chorioretinal atrophy: the mildest changes are located in the photoreceptor outer segment/retinal pigment epithelium junction.
    Jonasson F, Sander B, Eysteinsson T, Jörgensen T, Klintworth GK.
    Acta Ophthalmol Scand; 2007 Dec; 85(8):862-7. PubMed ID: 17683515
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