Xinping Yu

TL;DR: It is shown for the first time that compound heterozygous mutations in PROM1 gene could cause cone-rod dystrophy, and the enormous potential of CNGS in putative STGD molecular diagnosis is supported.

TL;DR: Macular vessel density is decreased in anisometropic amblyopia, and to a lesser extent, the other amblyopias, and correlations among these two variables were analyzed.

TL;DR: The SD-OCT data revealed marginal differences in some foveal layers at peripheral locations and indicated that structural differences might exist between individuals with amblyopia and visually normal control subjects, however, the differences were scattered and represented no identifiable pattern.

TL;DR: It is demonstrated that compound heterozygosity of two novel nonsense mutations in PDE6B could lead to RP, and the results collectively point to enormous potential of next-generation sequencing in determining the genetic etiology of RP and how various mutations in F6B contribute to the genetic heterogeneity of RP.

TL;DR: The 5-Fu-polycaprolactone sustained-release film had a sustained drug release effect, which promoted the inhibition of bleb scarring after Ahmed glaucoma valve implantation, and was significantly thinner than that of the other groups.