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Hyaloideoretinal degeneration of Wagner

Known as: WGVRP, Wagner Syndrome 1, Wagner vitreoretinal degeneration 
A form of vitreoretinopathy characterized by thinning (erosion) of the retinal pigment epithelium that permits increased visualization of the… 
National Institutes of Health

Related topics

Related topics

7 relations
Autosomal dominant inheritanceCataractChorioretinal atrophyGlaucoma

Broader (2)

Retinal DegenerationVersicans

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2017
Highly Cited
2017
Combination of Cp*RhIII -Catalyzed C-H Activation and a Wagner-Meerwein-Type Rearrangement.
A combination of Cp*RhIII -catalyzed C-H activation and Wagner-Meerwein-type rearrangement was successfully achieved for the… 
2015
2015
Metabolic Activity of Red Nucleus and Its Correlation with Cerebral Cortex and Cerebellum: A Study Using a High-Resolution Semiconductor PET System
The red nucleus (RN) is a pair of small gray matter structures located in the midbrain and involved in muscle movement and… 
Review
2014
Review
2014
Adorno’s Essay on Wagner: Rescuing an Inverted Panegyric
Theodor Adorno’s Versuch über Wagner stands after Nietzsche’s assorted polemics as perhaps the most sophisticated, provocative… 
2008
2008
Coarsening Kinetics of Mn-Doped CdSe Nanocrystals
CdSe and Mn-doped CdSe nanocrystals were synthesized by the inverse micelle technique using paraffin oil and oleic acid, and they… 
2006
2006
Hot Brains: Manipulating Body Heat to Save the Brain
Consider a disease with high mortality, severe morbidity, unknown pathogenesis, imprecise diagnostic features, and no known cure… 
2001
2001
The effects of moisture on the dielectric relaxation of urethane dimethacrylate polymer and composites.
Dielectric characterization evaluated the influence of sorbed moisture on urethane dimethacrylate (UDMA) polymer matrix and… 
2001
2001
Stickler syndrome and vitreoretinal degeneration: correlation between locus mutation and vitreous phenotype. Apropos of a case
Abstract. Background: Autosomal dominant vitreoretinopathies are characterized by genetic heterogeneity. Structural mutations in… 
1999
1999
Refined genetic and physical localization of the Wagner disease (WGN1) locus and the genes CRTL1 and CSPG2 to a 2- to 2.5-cM region of chromosome 5q14.3.
Wagner syndrome (WGN1; MIM 143200), an autosomal dominant vitreoretinopathy characterized by chorioretinal atrophy, cataract, and… 
1991
1991
Mesopithecus pentelicus Wagner aus dem Turolien von Pikermi bei Athen, Odontologie und Osteologie : (eine Dokumentation)
1941
1941
The fluorometric determination of riboflavin in urine and other biological fluids.
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