All Stories

  1. A rare form of ankyloblepharon filiforme adnatum associated with the Hay–Wells syndrome and a c.1709T>C mutation on the TP63 gene
  2. Evaluation of the WinROP system for identifying retinopathy of prematurity in Czech preterm infants
  3. A new modified technique for the treatment of high - risk prethreshold ROP under the direct visual control of RetCam 3