Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

Polymorphous corneal dystrophy

Known as: CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1, PPCD, CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT, FORMERLY 
This corneal dystrophy affects the posterior limiting membrane of the cornea and is characterized by polymorphous plaques of calcium deposits in the… Expand
National Institutes of Health

Related topics

Related topics

5 relations
Autosomal dominant inheritanceCOL8A2 geneCORNEAL ENDOTHELIAL DYSTROPHY 2Secondary glaucoma

Broader (1)

Hereditary corneal dystrophy

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
Tumor penetrability and anti-angiogenesis using iRGD-mediated delivery of doxorubicin-polymer conjugates.
Tumor-penetrating peptide, iRGD (internalizing RGD, CRGDK/RGPD/EC) with the similar affinity to αv integrins as conventional RGD… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
2011
Highly Cited
2011
RGD-modified PEG-PAMAM-DOX conjugates: in vitro and in vivo studies for glioma.
This work was based on our recent studies that a promising conjugate, RGD-modified PEGylated polyamidoamine (PAMAM) dendrimer… Expand
  • figure 1
  • table 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
Highly Cited
2010
Highly Cited
2010
Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p.
Fuchs corneal dystrophy (FCD) is a degenerative genetic disorder of the corneal endothelium that represents one of the most… Expand
  • figure 1
  • figure 2
  • table 1
  • table 2
  • figure 3
Is this relevant?
Highly Cited
2010
Highly Cited
2010
Partly PEGylated polyamidoamine dendrimer for tumor-selective targeting of doxorubicin: the effects of PEGylation degree and drug conjugation style.
Partly PEGylated polyamidoamine (PAMAM) dendrimers were used as the carrier for tumor-selective targeting of the anticancer drug… Expand
  • figure 1
  • figure 2
  • table 1
  • table 2
  • figure 3
Is this relevant?
Highly Cited
2010
Highly Cited
2010
Missense mutations in the sodium borate cotransporter SLC4A11 cause late‐onset Fuchs corneal dystrophy a
Homozygous mutations in the Borate Cotransporter SLC4A11 cause two early‐onset corneal dystrophies: congenital hereditary… Expand
Is this relevant?
Highly Cited
2008
Highly Cited
2008
SLC4A11 mutations in Fuchs endothelial corneal dystrophy.
The endothelial (posterior) corneal dystrophies, which result from primary endothelial dysfunction, include Fuchs endothelial… Expand
  • table 1
  • figure 1
  • table 2
  • figure 3
  • figure 2
Is this relevant?
Highly Cited
2008
Highly Cited
2008
Analysis of the posterior polymorphous corneal dystrophy 3 gene, TCF8, in late-onset Fuchs endothelial corneal dystrophy.
PURPOSE Because the endothelial (posterior) corneal dystrophies share common pathologic features and result from primary… Expand
  • table 1
  • figure 1
  • figure 2
Is this relevant?
Highly Cited
2005
Highly Cited
2005
Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells.
Posterior polymorphous corneal dystrophy (PPCD, also known as PPMD) is a rare disease involving metaplasia and overgrowth of… Expand
  • table 1
  • table 2
  • figure 1
  • figure 2
  • figure 3
Is this relevant?
Highly Cited
2004
Highly Cited
2004
Progressive posterior cortical dysfunction
Background: Atypical presentations of neurodegenerative dementing disorders include the syndrome of progressive posterior… Expand
  • table 1
  • table 1
  • table 2
Is this relevant?
Highly Cited
1995
Highly Cited
1995
Linkage of posterior polymorphous corneal dystrophy to 20q11.
Posterior polymorphous dystrophy (PPMD) is an autosomal dominant disorder of the cornea that is clinically recognized by the… Expand
Is this relevant?
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy, Terms of Service, and Dataset License
ACCEPT & CONTINUE