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175 681 (0,588s)

Result

Coincidental Occurrence of Schnyder Corneal Dystrophy and Posterior Polymorphous Corneal Dystrophy Type 3

This case illustrates the coincidental occurrence of 2 rare and genetically distinct corneal dystrophies in a single patient. Furthermore, It highlights the need to perform comprehensive phenotyping in combination with appropriate g...

Ophthalmology

  • 2019
  • Jimp
  • Link
Result

Immunohistochemical characterization of cytokeratins in the abnormal corneal endothelium of posterior polymorphous corneal dystrophy patiens

posterior polymorphous corneal dystrophy...

FF - ORL, oftalmologie, stomatologie

  • 2007
  • Jx
Result

Posterior Polymorphous Corneal Dystrophy: A Review of Current Knowledge

The chapter gives current information on the bac polymorphous corneal dystrophy...

FF - ORL, oftalmologie, stomatologie

  • 2009
  • C
Result

Novel mutations in the ZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy

posterior polymorphous cornea dystrophy...

FF - ORL, oftalmologie, stomatologie

  • 2007
  • Jx
Result

Posterior polymorphous corneal dystrophy in Czech families maps to chromosome 20 and excludes the VSX1 gene

corneal dystrophy...

FF - ORL, oftalmologie, stomatologie

  • 2005
  • Jx
Result

Descemet membrane endothelial keratoplasty with a stromal rim in the treatment of posterior polymorphous corneal dystrophy

Descemet membrane endothelial keratoplasty with a stromal rim was performed in a 20-year-old patient, diagnosed with posterior polymorphous corneal dystrophy....

FF - ORL, oftalmologie, stomatologie

  • 2012
  • Jx
  • Link
Result

Variable ocular phenotypes of posterior polymorphous corneal dystrophy caused by mutations in the ZEB1 gene

We describe the ocular features of Czech and British patients with posterior polomorphous corneal dystrophy caused by mutations in the zine finger E-box binding hemeobox 1 gene ( ZEB1)......

FF - ORL, oftalmologie, stomatologie

  • 2010
  • Jx
Result

Identification of Six Novel Mutations in ZEB1 and Description of the Associated Phenotypes in Patients with Posterior Polymorphous Corneal Dystrophy 3

Posterior polymorphous corneal dystrophy 3 (PPCD3) is a rare autosomal dominant had the c.1576dup; p.(Val526Glyfs*3) mutation previously reported in other populations. Clinical findings were varia...

EB - Genetika a molekulární biologie

  • 2015
  • Jx
  • Link
Result

Active Transforming Growth Factor-beta2 in the Aqueous Humor of Posterior Polymorphous Corneal Dystrophy Patients

Posterior polymorphous corneal dystrophy (PPCD) is characterized by abnormal proliferation of corneal endothelial cells. It was shown that TGF-beta2 present in aqueous humor (AH) could help maintaining the...

Statistics and probability

  • 2017
  • Jimp
  • Link
Result

Changes in the localization of collagens IV and VIII in corneas obtained from patients with posterior polymorphous corneal dystrophy

The aim of this study was to determine the changes in the presence and localization of the ?1 ? ?6 collagen IV and ?1, ?2 collagen VIII chains in Czech patients with posterior polymorphous corneal dystrophy (PPCD)....

FF - ORL, oftalmologie, stomatologie

  • 2009
  • Jx
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