Disease: Macular dystrophy- atypical vitelliform
- A case of Mac Tel 2 with an unusual sub macular vitelliform lesion
- A NOVEL P.ASP304GLY MUTATION IN BEST1 GENE ASSOCIATED WITH ATYPICAL BEST VITELLIFORM MACULAR DYSTROPHY PHENOTYPE AND HIGH INTRAFAMILIAL VARIABILITY
- Acute Exudative Polymorphous Vitelliform Maculopathy Syndrome; natural history and evolution of fundal and OCT images over time
- Adult onset Best's macular dystrophy (VMD2) with unilateral presentation
- An extended phenotype of <em>RP1L1</em> maculopathy - case report
- Atypical foveomacular vitelliform degeneration, adult type
- Atypical macular coloboma in a patient with adult vitelliform dystrophy
- Atypical presentation of Best Disease
- Atypical presentation of primary intraocular lymphoma
- Atypical presentations of Best's vitelliform macular degeneration: clinical findings in seven cases
- Atypical vitelliform disk. Apropos of a familial case
- Atypical vitelliform macular dystrophy in a 5-generation family
- Atypical vitelliform macular dystrophy misdiagnosed as chronic central serous chorioretinopathy: case reports
- Autosomal dominant Best disease with an unusual electrooculographic light rise and risk of angle-closure glaucoma: a clinical and molecular genetic study
- Autosomal recessive best vitelliform macular dystrophy: report of a family and management of early-onset neovascular complications
- BEST1 novel mutation causes Bestrophinopathies in six families with distinct phenotypic diversity
- BEST1 Variant Associated with an Atypical Macular and Peripheral Retinal Phenotype
- Clinical and genetic heterogeneity in Slovenian patients with BEST disease
- Clinical and molecular genetic analysis of best vitelliform macular dystrophy
- Electrooculography and optical coherence tomography reveal late-onset Best disease
- Exclusion of atypical vitelliform macular dystrophy from 8q24.3 and from other known macular degenerative loci
- Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sites
- Linkage of atypical vitelliform macular dystrophy (VMD-1) to the soluble glutamate pyruvate transaminase (GPT1) locus
- Linkage studies of Best's macular dystrophy
- Novel Mutation in BEST1 Associated with Atypical Best Vitelliform Dystrophy
- Phenotype and genotype of patients with autosomal recessive bestrophinopathy
- Presumed vitelliform dystrophy with perimacular flecks and retinal detachment
- Unilateral BEST1-Associated Retinopathy
- Value of neurophysiologic explorations in the diagnosis of atypical forms of vitelliform disks