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Journal Abstract Search

447 related items for PubMed ID: 30701423

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  • 2. Two cases of unilateral cone-rod dysfunction with negative electroretinograms.
    Ozawa K, Takahashi S, Mochizuki K, Miyake Y.
    Doc Ophthalmol; 2019 Dec; 139(3):247-256. PubMed ID: 31375969
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  • 3. Mitochondrial retinal dystrophy associated with the m.3243A>G mutation.
    de Laat P, Smeitink JAM, Janssen MCH, Keunen JEE, Boon CJF.
    Ophthalmology; 2013 Dec; 120(12):2684-2696. PubMed ID: 23806424
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  • 5. Multimodal imaging and functional correlations identify unusual cases of macular retinal pigment epithelium hypopigmentation occurring without functional loss.
    Boulanger-Scemama E, Akesbi J, Tick S, Mohand-Said S, Sahel JA, Audo I.
    Doc Ophthalmol; 2017 Aug; 135(1):77-83. PubMed ID: 28593392
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  • 9. Electroretinography and optical coherence tomography reveal abnormal post-photoreceptoral activity and altered retinal lamination in patients with enhanced S-cone syndrome.
    Sustar M, Perovšek D, Cima I, Stirn-Kranjc B, Hawlina M, Brecelj J.
    Doc Ophthalmol; 2015 Jun; 130(3):165-77. PubMed ID: 25663266
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  • 10. Detailed functional and structural phenotype of Bietti crystalline dystrophy associated with mutations in CYP4V2 complicated by choroidal neovascularization.
    Fuerst NM, Serrano L, Han G, Morgan JI, Maguire AM, Leroy BP, Kim BJ, Aleman TS.
    Ophthalmic Genet; 2016 Dec; 37(4):445-452. PubMed ID: 27028354
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  • 12. Macular dystrophy associated with the mitochondrial DNA A3243G mutation: pericentral pigment deposits or atrophy? Report of two cases and review of the literature.
    Daruich A, Matet A, Borruat FX.
    BMC Ophthalmol; 2014 Jun 06; 14():77. PubMed ID: 24906873
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  • 14. Spectral domain optical coherence tomography findings in bilateral peripheral cone dystrophy.
    Baek J, Lee HK, Kim US.
    Doc Ophthalmol; 2013 Jun 06; 126(3):247-51. PubMed ID: 23456543
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  • 15. Outer retina analysis by optical coherence tomography in cone-rod dystrophy patients.
    Lima LH, Sallum JM, Spaide RF.
    Retina; 2013 Oct 06; 33(9):1877-80. PubMed ID: 23648999
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  • 17. Cone structure in retinal degeneration associated with mutations in the peripherin/RDS gene.
    Duncan JL, Talcott KE, Ratnam K, Sundquist SM, Lucero AS, Day S, Zhang Y, Roorda A.
    Invest Ophthalmol Vis Sci; 2011 Mar 01; 52(3):1557-66. PubMed ID: 21071739
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  • 18. Multimodal imaging analysis of macular dystrophy in patient with maternally inherited diabetes and deafness (MIDD) with m.3243A>G mutation.
    Oishi N, Kubota D, Nakamoto K, Takeda Y, Hayashi M, Gocho K, Yamaki K, Igarashi T, Takahashi H, Kameya S.
    Ophthalmic Genet; 2021 Jun 01; 42(3):304-311. PubMed ID: 33541179
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  • 19. Retinal dystrophy and subretinal drusenoid deposits in female choroideremia carriers.
    Murro V, Mucciolo DP, Passerini I, Palchetti S, Sodi A, Virgili G, Rizzo S.
    Graefes Arch Clin Exp Ophthalmol; 2017 Nov 01; 255(11):2099-2111. PubMed ID: 28752371
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  • 20. Phenotypic findings in C1QTNF5 retinopathy (late-onset retinal degeneration).
    Soumplis V, Sergouniotis PI, Robson AG, Michaelides M, Moore AT, Holder GE, Webster AR.
    Acta Ophthalmol; 2013 May 01; 91(3):e191-5. PubMed ID: 23289492
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