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Journal Abstract Search

151 related items for PubMed ID: 38111473

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  • 3. Localized retinal electrophysiological and fundus autofluorescence imaging abnormalities in maternal inherited diabetes and deafness.
    Bellmann C, Neveu MM, Scholl HP, Hogg CR, Rath PP, Jenkins S, Bird AC, Holder GE.
    Invest Ophthalmol Vis Sci; 2004 Jul; 45(7):2355-60. PubMed ID: 15223817
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  • 5. Mitochondrial Retinopathy.
    Birtel J, von Landenberg C, Gliem M, Gliem C, Reimann J, Kunz WS, Herrmann P, Betz C, Caswell R, Nesbitt V, Kornblum C, Charbel Issa P.
    Ophthalmol Retina; 2022 Jan; 6(1):65-79. PubMed ID: 34257060
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  • 6. 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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  • 13. Structural Features Associated With the Development and Progression of RORA Secondary to Maternally Inherited Diabetes and Deafness.
    Müller PL, Maloca P, Webster A, Egan C, Tufail A.
    Am J Ophthalmol; 2020 Oct 06; 218():136-147. PubMed ID: 32446735
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  • 14. 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 06; 37(4):445-452. PubMed ID: 27028354
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  • 15. Morphologic characteristics of the outer retina in cone dystrophy on spectral-domain optical coherence tomography.
    Cho SC, Woo SJ, Park KH, Hwang JM.
    Korean J Ophthalmol; 2013 Feb 06; 27(1):19-27. PubMed ID: 23372375
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  • 18. Cystoid macular changes on optical coherence tomography in a patient with maternally inherited diabetes and deafness (MIDD)-associated macular dystrophy.
    Qian CX, Branham K, Khan N, Lundy SK, Heckenlively JR, Jayasundera T.
    Ophthalmic Genet; 2017 Feb 06; 38(5):467-472. PubMed ID: 28140742
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