Disease: Vitreoretinochoroidopathy dominant
- A novel missense mutation in BEST1 associated with an autosomal-dominant vitreoretinochoroidopathy (ADVIRC) phenotype
- ADVIRC is caused by distinct mutations in BEST1 that alter pre-mRNA splicing
- Autosomal dominant vitreoretinochoroidopathy
- Autosomal dominant vitreoretinochoroidopathy
- Autosomal dominant vitreoretinochoroidopathy (ADVIRC)
- Autosomal Dominant Vitreoretinochoroidopathy With a Novel BEST1 Mutation and a Review of Reported Mutations
- Autosomal dominant vitreoretinochoroidopathy with normal electrooculogram in a German family
- AUTOSOMAL DOMINANT VITREORETINOCHOROIDOPATHY: When Molecular Genetic Testing Helps Clinical Diagnosis
- Autosomal dominant vitreoretinochoroidopathy. Report of the third family
- BEST1-related autosomal dominant vitreoretinochoroidopathy: a degenerative disease with a range of developmental ocular anomalies
- Bestrophin 1 and retinal disease
- Bestrophinopathies
- Biallelic mutation of BEST1 causes a distinct retinopathy in humans
- Calpain-5 mutations cause autoimmune uveitis, retinal neovascularization, and photoreceptor degeneration
- CAPN5 genetic inactivation phenotype supports therapeutic inhibition trials
- Central cone dysfunction in autosomal dominant vitreoretino choroidopathy (ADVIRC)
- Clinical and electrophysiological findings in autosomal dominant vitreoretinochoroidopathy: report of a new pedigree
- Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)
- Clinical features of the congenital vitreoretinopathies
- Comment: A novel missense mutation in BEST1 associated with an autosomal-dominant vitreoretinochoroidopathy (ADVIRC) phenotype
- Disease-causing mutations associated with four bestrophinopathies exhibit disparate effects on the localization, but not the oligomerization, of Bestrophin-1
- Electro-oculography in autosomal dominant vitreoretinochoroidopathy
- Fundus Autofluorescence and SD-OCT Document Rapid Progression in Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Associated with a c.256G > A Mutation in BEST1
- Fundus Autofluorescence and SD-OCT Document Rapid Progression in Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Associated with a c.256G > A Mutation in BEST1
- Hereditary retinochoroidal dystrophies. Part 2: differential diagnosis
- Histopathologic study of autosomal dominant vitreoretinochoroidopathy in a 26-year-old woman
- Histopathologic study of autosomal dominant vitreoretinochoroidopathy. Peripheral annular pigmentary dystrophy of the retina
- Long-term changes in autosomal dominant vitreoretinochoroidopathy (ADVIRC)
- Long-Term Macular Changes in the First Proband of Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Due to a Newly Identified Mutation in BEST1
- Mislocalisation of BEST1 in iPSC-derived retinal pigment epithelial cells from a family with autosomal dominant vitreoretinochoroidopathy (ADVIRC)
- Molecular evolution and functional divergence of the bestrophin protein family
- Mutation-Dependent Pathomechanisms Determine the Phenotype in the Bestrophinopathies
- Mutations of VMD2 splicing regulators cause nanophthalmos and autosomal dominant vitreoretinochoroidopathy (ADVIRC)
- Ocular Histopathology and Immunohistochemical Analysis in the Oldest Known Individual with Autosomal Dominant Vitreoretinochoroidopathy
- Plasmin Enzyme-Assisted Vitrectomy in Pediatric Patients with Vitreoretinal Diseases
- Progressive Cone Dysfunction and Geographic Atrophy of the Macula in Late Stage Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC)
- Response to Weisschuh's "Comment: a novel missense mutation in BEST1 associated with an autosomal-dominant vitreoretinochoroidopathy (ADVIRC) phenotype"
- Retinitis pigmentosa associated with a mutation in BEST1
- Revolution in evolution
- The anion-selective pore of the bestrophins, a family of chloride channels associated with retinal degeneration
- The Best Retinitis Pigmentosa Masquerade
- The incidence and risk factors for the development of vitreomacular interface abnormality in diabetic macular edema treated with intravitreal injection of anti-VEGF
- The light peak of the electroretinogram is dependent on voltage-gated calcium channels and antagonized by bestrophin (best-1)
- The spectrum of ocular phenotypes caused by mutations in the BEST1 gene
- Variable expressivity of <em>BEST1</em>-associated autosomal dominant vitreoretinochoroidopathy (ADVIRC) in a three-generation pedigree
- Variable expressivity of BEST1-associated autosomal dominant vitreoretinochoroidopathy (ADVIRC) in a three-generation pedigree
- Variable expressivity of the autosomal dominant vitreoretinochoroidopathy (ADVIRC) phenotype associated with a novel variant in BEST1
- Vitreoretinochoroidal heredo-dystrophy, microcornea, glaucoma and cataract
- VMD2 and its role in Best's disease and other retinopathies
- Whole-exome sequencing identified ARL2 as a novel candidate gene for MRCS (microcornea, rod-cone dystrophy, cataract, and posterior staphyloma) syndrome