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The Role of Kynurenine and 5-Hydroxytryptophan in Modulating Microbiota and Their Implications in Exudative Age-Related Macular Degeneration. [PDF]
Diagnostics (Basel)Vilkeviciute-Petraite A +7 more
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Machine-learning for age-related macular degeneration using multimodal fundus data. [PDF]
Front Med (Lausanne)Li M +6 more
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Hemolytic Glaucoma Following Intravitreal Aflibercept Injection for Age-Related Macular Degeneration: A Case Report. [PDF]
Am J Case RepSano H, Yanai R, Mitamura Y.
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AMD-UPerNet: a tool for retinal layer and fluid assessment in age-related macular degeneration. [PDF]
BMC Med ImagingMa Q +7 more
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Neovascular age-related macular degeneration without drusen. [PDF]
Acta OphthalmolSirks MJ +9 more
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PCSK9 Inhibitor Use and the Risk of Age-Related Macular Degeneration in Patients with Atherosclerotic Cardiovascular Disease. [PDF]
Pharmaceuticals (Basel)Tsai HR, Hsu JZ, Loh CH, Huang HK.
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Annual Review of Medicine, 2007
Macular degeneration is a term that describes a large group of conditions that are collectively the most common cause of irreversible vision loss in the developed world. Approximately one in three people will be affected to some degree by the time they reach 75 years of age.
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Macular degeneration is a term that describes a large group of conditions that are collectively the most common cause of irreversible vision loss in the developed world. Approximately one in three people will be affected to some degree by the time they reach 75 years of age.
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PSEUDOVITELLIFORM MACULAR DEGENERATION
Retina, 1982Forty-two patients with pseudovitelliform macular degeneration (VMD) were studied. The macular lesions were yellow in color, appeared as a slight elevation at the level of the retinal pigment epithelium (RPE), were usually 1/4 to 1/2 disc diameter in size and often showed a round or oval shape.
R, Sabates, R C, Pruett, T, Hirose
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Vitelliform Macular Degeneration
American Journal of Ophthalmology, 1977Six patients had macular vitelliform lesions similar to those in Best's vitelliform foveal dystrophy but all had normal electro-oculograms (EOG) and no familial involvement. Two patients had an exudative form of degenerative chroidopathy. The remining four had vitelliform lesions of unknown etiology.
J D, Kingham, G P, Lochen
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