Sentence examples for mid periphery of from inspiring English sources

Experimental studies in animals and clinical observations have suggested that the afferent sensory part may be located in the mid periphery of the fundus in the retro-equatorial region of the eye [39, 40].

© 2010 Wiley-Liss, Inc. Retinitis pigmentosa (RP) is a heterogeneous group of inherited retinal dystrophies featured by the loss of photoreceptor cells and clinically characterized by pigmentory deposits at mid periphery of the retina that are visible on fundus examination.

The exit wounds were larger than the entrance ones and located as follows: transfoveal (case 8), nasally to the optic disc (case 16) and inferior, in the mid periphery of the retina (case 17).

Rod and cone photoreceptor cells start to degenerate from the mid periphery to the far periphery and the centre of the retina, resulting in the so-called tunnel vision.

Four years after initial presentation, new serous RPE detachments had developed in the mid-periphery of both eyes (figure 1G,H).

In this study, intrastromal ablation was performed in the mid-periphery of the anterior cornea with a 10-μm spot/line and 45-μm layer separation whereby the unconnected microbubbles were generated between and among the layers.

In 1971, Worst first presented the iris-claw lens (a biconvex polymethyl methacrylate IOL fixated above the iridal plane at the mid-periphery of the iris) at a meeting in Paris [ 1].

The aim of this study is to observe the refractive change in the adult rabbits undergoing femtosecond laser-assisted multilayer intrastromal ablation in the mid-periphery of the cornea without injury of epithelium.

In the interface of the applanation contact lens cone, a 6-mm diameter aluminum circle was placed at the center to block the laser, limiting ablation to the mid-periphery of the cornea.

In a previous study [ 5], we demonstrated the morphological and histopathologic changes to the immature rabbit cornea after multi-layer ablation of the stroma with the FSL at different depths in the mid-periphery of the cornea, which may not have been definitive because of immaturity of the cornea.

Stargardt disease (STGD, MIM #248200) is the most common hereditary macular dystrophy, with an estimated prevalence of 1 10 000. 1 It is characterised by onset in the juvenile to young adult years, decreased central vision, progressive bilateral atrophy of the retinal pigment epithelium (RPE) and the appearance of orange-yellow flecks around the macula and/or mid-periphery of the retina.