Disease: Hyaloideoretinal degeneration of Wagner
- A family with Wagner syndrome with uveitis and a new versican mutation
- A new VCAN/versican splice acceptor site mutation in a French Wagner family associated with vascular and inflammatory ocular features
- Circumferential equatorial vitreous veil in a patient with Wagner syndrome
- Clinical and genetic study on two Chinese families with Wagner vitreoretinopathy
- Complex Combined Tractional and Rhegmatogenous Retinal Detachment in a Twenty-Three-Year-Old Male With Wagner Syndrome
- Congenital glaucoma in Wagner syndrome
- De novo splice mutation in the versican gene in a family with Wagner syndrome
- Deletions Overlapping VCAN Exon 8 Are New Molecular Defects for Wagner Disease
- Features of genetic mutations in children with high myopia combined with peripheral retinal degenerations
- Giant retinal tears treated with lens sparing, bimanual 23 g vitrectomy without scleral buckle
- Identification of Novel Copy Number Variations of VCAN Gene in Three Chinese Families with Wagner Disease
- Is exon 8 the most critical or the only dispensable exon of the VCAN gene? Insights into VCAN variants and clinical spectrum of Wagner syndrome
- Multimodal Imaging in Wagner Syndrome
- Multimodal Retinal Imaging Findings in Two Cousins With VCAN-Related Vitreoretinopathy or Wagner Disease
- Mutation in collagen II alpha 1 isoforms delineates Stickler and Wagner syndrome phenotypes
- Spectral-Domain Optical Coherence Tomography in Wagner Syndrome: Characterization of Vitreoretinal Interface and Foveal Changes
- Stickler and Wagner Syndrome in African Americans
- VCAN Canonical Splice Site Mutation is Associated With Vitreoretinal Degeneration and Disrupts an MMP Proteolytic Site
- WAGNER syndrome: anatomic, functional and genetic characterization of a Portuguese family
- WAGNER'S DISEASE
- WIDEFIELD SWEPT-SOURCE OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY FINDINGS IN WAGNER SYNDROME