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Fuchs Endothelial Dystrophy

Known as: dystrophia epithelialis corneae, dystrophy fuch, Endothelial Dystrophy, Fuch's 
An autosomal dominant, bilateral, slowly progressive degeneration of corneal endothelial cells with thickening of Descemet's membrane and… 
National Institutes of Health

Related topics

Related topics

22 relations

Narrower (7)

CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 5CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 7Cornea guttata with anterior polar cataract
Chandler syndromeCorneaCorneal dystrophy, epithelial basement membraneEye

Broader (4)

Corneal DiseasesCorneal dystrophyHereditary DiseasesHereditary corneal dystrophy

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2006
Review
2006
Review: Werner Fuchs-Heinritz (2005). Biographische Forschung. Eine Einführung in Praxis und Methoden
Werner FUCHS-HEINRITZ verschreibt sich dem Ziel, in die Grundlagen der Biographieforschung einzufuhren. Konturiert werden Formen… 
Review
2005
Review
2005
Endothelial microparticles (EMP) as vascular disease markers.
2005
2005
CYP4V2 Mutations in Two Japanese Patients with Bietti’s Crystalline Dystrophy
Bietti’s crystalline dystrophy (BCD) is an autosomal-recessive retinal dystrophy characterized by numerous glistening… 
Highly Cited
2004
Highly Cited
2004
Systemic axonal dystrophy in vitamin E deficient adult rats
Interes t in v i tamin E deficiency was great ly s t imulated when GO~TTSC~ and PA~P~n~IME~ reported the development of "nutr i t… 
Highly Cited
2003
Highly Cited
2003
A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13
Asphyxiating thoracic dystrophy (ATD), or Jeune syndrome, is a multisystem autosomal recessive disorder associated with a… 
Highly Cited
1995
Highly Cited
1995
Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6q.
Progressive bifocal chorioretinal atrophy (PBCRA) is a rare, autosomal dominant congenital chorioretinal dystrophy. We have… 
Highly Cited
1992
Highly Cited
1992
The effect of cytokines and chemotactic agonists on the migration of T lymphocytes into skin.
The migration of lymphocytes and neutrophils into skin sites stimulated with chemotactic agonists or with cytokines known to… 
Highly Cited
1991
Highly Cited
1991
Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker.
We have examined the linkage of two new polymorphic DNA markers (D19S62 and D19S63) and a previously unreported polymorphism with… 
Highly Cited
1985
Highly Cited
1985
Profound limb deficiency, thoracic dystrophy, unusual facies, and normal intelligence: a new syndrome.
A newly recognised profound limb deficiency malformation syndrome in two Arab sibs of different sexes with consanguineous parents… 
1976
1976
The effects of light and dark adaptation on the levels of cyclic nucleotides in retinas of mice heterozygous for a gene for photoreceptor dystrophy.
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