Wagner Syndrome Latest Advances

Expression of Versican in the Retina and Its Implication in Retinal Disease.

Journal: Advances in experimental medicine and biology

Published: February 10, 2025

Multimodal Evaluation and Management of Wagner Syndrome-Three Patients from an Affected Family.

Journal: Genes

Published: August 02, 2024

Features of genetic mutations in children with high myopia combined with peripheral retinal degenerations

Journal: Vestnik oftalmologii

Published: March 07, 2024

Stickler and Wagner Syndrome in African Americans.

Journal: Ophthalmic surgery, lasers & imaging retina

Published: February 13, 2023

Multimodal Retinal Imaging Findings in Two Cousins With VCAN-Related Vitreoretinopathy or Wagner Disease.

Journal: Ophthalmic surgery, lasers & imaging retina

Published: November 15, 2022

WIDEFIELD SWEPT-SOURCE OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY FINDINGS IN WAGNER SYNDROME.

Journal: Retinal cases & brief reports

Published: August 25, 2022

Circumferential equatorial vitreous veil in a patient with Wagner syndrome.

Journal: Journal francais d'ophtalmologie

Published: May 03, 2022

Identification of Novel Copy Number Variations of VCAN Gene in Three Chinese Families with Wagner Disease.

Journal: Genes

Published: July 20, 2020

Clinical and genetic study on two Chinese families with Wagner vitreoretinopathy.

Journal: Ophthalmic genetics

Published: July 07, 2020

Complex Combined Tractional and Rhegmatogenous Retinal Detachment in a Twenty-Three-Year-Old Male With Wagner Syndrome.

Journal: Ophthalmic surgery, lasers & imaging retina

Published: December 04, 2019

VCAN Canonical Splice Site Mutation is Associated With Vitreoretinal Degeneration and Disrupts an MMP Proteolytic Site.

Journal: Investigative ophthalmology & visual science

Published: January 19, 2019

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.

Journal: American journal of medical genetics. Part A

Published: November 09, 2017

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Expression of Versican in the Retina and Its Implication in Retinal Disease.

Expression of Versican in the Retina and Its Implication in Retinal Disease.

Multimodal Evaluation and Management of Wagner Syndrome-Three Patients from an Affected Family.

Multimodal Evaluation and Management of Wagner Syndrome-Three Patients from an Affected Family.

Features of genetic mutations in children with high myopia combined with peripheral retinal degenerations

Features of genetic mutations in children with high myopia combined with peripheral retinal degenerations

Stickler and Wagner Syndrome in African Americans.

Stickler and Wagner Syndrome in African Americans.

Multimodal Retinal Imaging Findings in Two Cousins With VCAN-Related Vitreoretinopathy or Wagner Disease.

Multimodal Retinal Imaging Findings in Two Cousins With VCAN-Related Vitreoretinopathy or Wagner Disease.

WIDEFIELD SWEPT-SOURCE OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY FINDINGS IN WAGNER SYNDROME.

WIDEFIELD SWEPT-SOURCE OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY FINDINGS IN WAGNER SYNDROME.

Circumferential equatorial vitreous veil in a patient with Wagner syndrome.

Circumferential equatorial vitreous veil in a patient with Wagner syndrome.

Identification of Novel Copy Number Variations of VCAN Gene in Three Chinese Families with Wagner Disease.

Identification of Novel Copy Number Variations of VCAN Gene in Three Chinese Families with Wagner Disease.

Clinical and genetic study on two Chinese families with Wagner vitreoretinopathy.

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.

Complex Combined Tractional and Rhegmatogenous Retinal Detachment in a Twenty-Three-Year-Old Male With Wagner Syndrome.

VCAN Canonical Splice Site Mutation is Associated With Vitreoretinal Degeneration and Disrupts an MMP Proteolytic Site.

VCAN Canonical Splice Site Mutation is Associated With Vitreoretinal Degeneration and Disrupts an MMP Proteolytic Site.

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.

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.