A Case of Idiopathic Perifoveal Telangiectasia Preceded by Features of Cone Dystrophy

Eye - United Kingdom
doi 10.1038/sj.eye.6703011
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

Clinical Features of a Pediatric Case With Cone Dystrophy

Van Medical Journal
2018English

Perifoveal Müller Cell Depletion in a Case of Macular Telangiectasia Type 2

Ophthalmology
Ophthalmology
2010English

Ophthalmic Features of Cone-Rod Dystrophy Caused by Pathogenic Variants in the ALMS1 Gene

Acta Ophthalmologica
MedicineOphthalmology
2017English

Cone Beam Computed Tomography Features of Cherubism: A Case Report

International Journal of Medical and Dental Case Reports
2017English

Imaging Features of Idiopathic Granulomatous Mastitis – Case Report

Revista da Associacao Medica Brasileira
Medicine
2016English

Clinical Course of Cone Dystrophy Caused by Mutations in the RPGR Gene

Graefe's Archive for Clinical and Experimental Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2011English

Cone Dystrophy in Patient With HomozygousRP1L1Mutation

BioMed Research International
ImmunologyMolecular BiologyBiochemistryMicrobiology MedicineGenetics
2015English

Spondylometaphyseal Dysplasia-Cone-Rod Dystrophy Syndrome

2020English

Novel C8ORF37 Mutation Causing Cone Rod Dystrophy

Acta Ophthalmologica
MedicineOphthalmology
2018English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy