Disease: Best vitelliform macular dystrophy
- <em>IMPG2</em>-associated unilateral adult onset vitelliform macular dystrophy
- A case of recurring acute exudative polymorphous vitelliform maculopathy successfully treated with intravitreal Ozurdex injection
- A customized regimen of intravitreal aflibercept for the treatment of choroidal neovascularization secondary to different chorioretinal diseases
- A novel variant of autosomal recessive best vitelliform macular dystrophy and management of early-onset complications
- Acute exudative paraneoplastic polymorphous vitelliform maculopathy presenting as a masquerade syndrome
- ACUTE EXUDATIVE POLYMORPHOUS VITELLIFORM MACULOPATHY AS THE INITIAL PRESENTATION OF HUMAN IMMUNODEFICIENCY VIRUS INFECTION
- Acute exudative polymorphous vitelliform maculopathy during pembrolizumab treatment for metastatic melanoma: a case report
- ADULT-ONSET BEST1 -VITELLIFORM DYSTROPHY ASSOCIATED WITH ANGIOID STREAK-LIKE CHANGES IN TWO SIBLINGS
- Adult-onset foveomacular vitelliform dystrophy: epidemiology, pathophysiology, imaging, and prognosis
- An extended phenotype of <em>RP1L1</em> maculopathy - case report
- Application of patient-derived induced pluripotent stem cells and organoids in inherited retinal diseases
- Artificial Intelligence (AI) for Early Diagnosis of Retinal Diseases
- Asymmetric Best's disease in a 48-year-old man
- Best Disease
- Best Disease
- BEST Disease and Gene Therapy
- Best disease presenting as subretinal pigment epithelium hyperreflectivite lesion on spectral-domain optical coherence tomography: Multimodal imaging features
- Best Disease: Global Mutations Review, Genotype-Phenotype Correlation, and Prevalence Analysis in the Israeli Population
- Best macular dystrophy complicated by macular neovascularization: Case report of a young woman with CLOVES syndrome
- Best Vitelliform Macular Dystrophy (BVMD) is a phenocopy of North Carolina Macular Dystrophy (NCMD/MCDR1)
- Best Vitelliform Macular Dystrophy Natural History Study Report 1: Clinical Features and Genetic Findings
- BEST1 novel mutation causes Bestrophinopathies in six families with distinct phenotypic diversity
- BEST1 Variant Associated with an Atypical Macular and Peripheral Retinal Phenotype
- Bilateral consecutive choroidal neovascularization in Best vitelliform macular dystrophy
- Bilateral phacoemulsification with hyperaspheric intraocular lens in adult vitelliform macular dystrophy: A single case report
- Bilateral, Solitary, Extramacular Vitelliform Retinal Lesions in a Patient With Best Disease
- Choroidal Neovascularization Associated with Best Vitelliform Macular Dystrophy
- Choroidal neovascularization associated with butterfly-shaped pattern dystrophy - a case report
- Choroidal Neovascularization Is Common in Best Vitelliform Macular Dystrophy and Plays a Role in Vitelliform Lesion Evolution
- CHOROIDAL NEVUS ASSOCIATED WITH VITELLIFORM DEPOSITION IN A PATIENT WITH AUTOSOMAL DOMINANT BEST DYSTROPHY
- Clinical and visual electrophysiological characteristics of vitelliform macular dystrophies in the first decade of life
- Clinical Correlation Between Optical Coherence Tomography Biomarkers and Retinal Sensitivity in Best Vitelliform Macular Dystrophy
- Clinical features and possible pathogenesis of multiple evanescent white dot syndrome with different retinal diseases and events: a narrative review
- Clinical findings in eyes with BEST1-related retinopathy complicated by choroidal neovascularization
- Cloudy Vitelliform Submaculopathy as an Early Sign of Primary Vitreoretinal Lymphoma
- Combination of Trabeculectomy and Primary Pars Plana Vitrectomy in the Successful Treatment of Angle-Closure Glaucoma with BEST1 Mutations: Self-Controlled Case Series
- Condition optimization of eco-friendly RP-HPLC and MCR methods via Box-Behnken design and six sigma approach for detecting antibiotic residues
- Coronavirus Disease 2019-induced Acute Exudative Polymorphous Vitelliform Maculopathy
- Correlation of features on OCT with visual acuity and Gass lesion type in Best vitelliform macular dystrophy
- COVID-19 VACCINE-INDUCED ACUTE EXUDATIVE POLYMORPHOUS VITELLIFORM MACULOPATHY: CASE REPORTS
- CRISPR/Cas9 mediated specific ablation of vegfa in retinal pigment epithelium efficiently regresses choroidal neovascularization
- Cytology-Proven Primary Vitreoretinal Lymphoma in a Patient With Paraneoplastic Cloudy Vitelliform Submaculopathy
- Deep learning to distinguish Best vitelliform macular dystrophy (BVMD) from adult-onset vitelliform macular degeneration (AVMD)
- Disease expression caused by different variants in the BEST1 gene: genotype and phenotype findings in bestrophinopathies
- Elaborate Evaluation of Farnsworth Dichotomous D-15 Panel Test Can Help Differentiate between Best Vitelliform Macular Dystrophy and Autosomal Recessive Bestrophinopathy
- Elaborate evaluation of Farnsworth Dichotomous D-15 Panel Test can help to differentiate between Best vitelliform macular dystrophy and autosomal recessive bestrophinopathy
- Expanded Clinical Spectrum of Pentosan Polysulfate Maculopathy: A Macula Society Collaborative Study
- Fixation Location and Stability in Best Vitelliform Macular Dystrophy
- Genetic and clinical features of BEST1-associated retinopathy based on 59 Chinese families and database comparisons
- Identification of a Complex Allele in IMPG2 as a Cause of Adult-Onset Vitelliform Macular Dystrophy
- Impaired Bestrophin Channel Activity in an iPSC-RPE Model of Best Vitelliform Macular Dystrophy (BVMD) from an Early Onset Patient Carrying the P77S Dominant Mutation
- IMPG2-associated unilateral adult onset vitelliform macular dystrophy
- IMPG2-related maculopathy
- Intracapsular hemorrhage in the setting of pseudoexfoliation syndrome
- Intravitreal bevacizumab treatment for exudative choroidal neovascularisation in best vitelliform macular dystrophy
- Lack of Response to Intravitreal Ranibizumab Treatment in Adult Onset Foveomacular Vitelliform
- Lack of Response to Intravitreal Ranibizumab Treatment in Adult Onset Foveomacular Vitelliform Dystrophy Complicated with Choroidal Neovascularization: A Case Report
- LONG-TERM PRESERVATION OF VISUAL ACUITY AFTER RESORPTION OF ACQUIRED VITELLIFORM LESIONS IN AGE-RELATED MACULAR DEGENERATION
- Multimodal imaging analysis of autosomal recessive bestrophinopathy: Case series
- Multimodal imaging and genetic analysis of adult-onset best vitelliform macular dystrophy in Chinese patients
- Multimodal Imaging Characteristics of Quiescent Type 1 Neovascularization in Best Vitelliform Macular Dystrophy
- Multimodal imaging in a case of best vitelliform macular dystrophy
- Multimodal imaging in Best Vitelliform Macular Dystrophy: Literature review and novel insights
- Nationwide epidemiologic survey on incidence of macular dystrophy in Japan
- New Noncoding Base Pair Mutation at the Identical Locus as the Original NCMD/MCDR1 in a Mexican Family, Suggesting a Mutational Hotspot
- Novel <em>IMPG2</em> variant causing adult macular vitelliform dystrophy: A case report
- Novel IMPG2 variant causing adult macular vitelliform dystrophy: A case report
- Novel mutations in the <em>BEST1</em> gene cause distinct retinopathies in two Chinese families
- Optical coherence tomography findings and choroidal neovascular membrane detectability with optical coherence tomography angiography in different subtypes of pattern dystrophy
- Optical Coherence Tomography in Inherited Macular Dystrophies: A Review
- Optical Coherence Tomography-Based Choroidal Structural Analysis and Vascularity Index in Best Vitelliform Macular Dystrophy
- Paradoxical autosomal recessive bestrophinopathy-like phenotypes shown in an autosomal dominant pedigree
- Persistent macular oedema following Best vitelliform macular dystrophy undergoing anti-VEGF treatment
- Phenotypic and Genetic Spectrum of Autosomal Recessive Bestrophinopathy and Best Vitelliform Macular Dystrophy
- Photoreceptor and Retinal Pigment Epithelium Relationships in Eyes With Vitelliform Macular Dystrophy Revealed by Multimodal Adaptive Optics Imaging
- Photoreceptor Function and Structure in Autosomal Dominant Vitelliform Macular Dystrophy Caused by BEST1 Mutations
- Primary and secondary focal choroidal excavation morphologic phenotypes, associated ocular disorders and prognostic implications
- Pseudovitelliform maculopathy associated with hereditary hemochromatosis
- Quantitative microvascular alterations in butterfly-shaped pattern dystrophy and adult-onset foveomacular vitelliform dystrophy
- Reliable estimation of internal oscillator properties from a novel, fast-paced tapping paradigm
- Retinal Dystrophies Associated With Peripherin-2: Genetic Spectrum and Novel Clinical Observations in 241 Patients
- Retinal Metabolic Profile on IMPG2 Deficiency Mice with Subretinal Lesions
- Retinal Pattern Dystrophy
- Retinal Pattern Dystrophy
- Retinal sensitivity and fundus autofluorescence in adult-onset foveomacular vitelliform dystrophy
- Risk Factors for Worsening Morphology and Visual Acuity in Eyes with Adult-Onset Foveomacular Vitelliform Dystrophy
- RPE-Directed Gene Therapy Improves Mitochondrial Function in Murine Dry AMD Models
- Scleral Thickness in Autosomal Dominant Best Vitelliform Macular Dystrophy
- SPACR Encoded by <em>IMPG1</em> Is Essential for Photoreceptor Survival by Interplaying between the Interphotoreceptor Matrix and the Retinal Pigment Epithelium
- Stage-dependent choriocapillaris impairment in Best vitelliform macular dystrophy characterized by optical coherence tomography angiography
- Temporary Vitelliform Regression After Intravitreal Ranibizumab Injection for Macular Neovascularization Complicating Best Disease
- The pseudohypopyon stage in adult-onset foveomacular vitelliform dystrophy
- The Retinal Phenotype Associated with the p.Pro101Thr BEST1 Variant
- Torpedo Maculopathy. A Case Report
- Typical best vitelliform dystrophy secondary to biallelic variants in BEST1
- Variants of BEST1 and CRYBB2 cause a complex ocular phenotype comprising microphthalmia, microcornea, cataract, and vitelliform macular dystrophy: case report
- Varied clinical presentations of RP1L1 variants in Chinese patients: a study of occult macular dystrophy and vitelliform macular dystrophy
- Vitelliform maculopathy in MELAS syndrome
- Vitelliform maculopathy: Diverse etiologies originating from one common pathway
- Whole exome sequencing identifies a novel splice-site mutation in IMPG2 gene causing Stargardt-like juvenile macular dystrophy in a north Indian family