Fuchs' endothelial corneal dystrophy: pathology and treatment outcome

This publication has 101 references indexed in Scilit:

• Decline in DJ-1 and Decreased Nuclear Translocation of Nrf2 in Fuchs Endothelial Corneal Dystrophy
  Investigative Ophthalmology & Visual Science, 2012
• The genetics of Fuchs’ corneal dystrophy
  Expert Review of Ophthalmology, 2012
• Visual Performance with Wave Aberration Correction after Penetrating, Deep Anterior Lamellar, or Endothelial Keratoplasty
  Investigative Ophthalmology & Visual Science, 2012
• The impact of the unfolded protein response on human disease
  Journal of Cell Biology, 2012
• Mutations in LOXHD1, a Recessive-Deafness Locus, Cause Dominant Late-Onset Fuchs Corneal Dystrophy
  The American Journal of Human Genetics, 2012
• A cellular model for the investigation of Fuchs' Endothelial Corneal Dystrophy
  Experimental Eye Research, 2011
• An alpha 2 collagen VIII transgenic knock-in mouse model of Fuchs endothelial corneal dystrophy shows early endothelial cell unfolded protein response and apoptosis
  Human Molecular Genetics, 2011
• Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophya
  Human Mutation, 2010
• Unfolded Protein Response in Fuchs Endothelial Corneal Dystrophy: A Unifying Pathogenic Pathway?
  American Journal of Ophthalmology, 2010
• Missense Mutations in TCF8 Cause Late-Onset Fuchs Corneal Dystrophy and Interact with FCD4 on Chromosome 9p
  The American Journal of Human Genetics, 2010