ISSN (On-line) 1678-2925
Home
About
Brief History
Open Science Compliance
Publication Ethics
Focus and Scope
Digital Preservation
Editorial Policy
Ethics Committee
Copyright License
Issues
Current Issue
Previous
Supplements
Ahead of print
COMMENTED PAPERS - EDITORS CHOICE
Advanced Search
Editorial Board
Submission
Instructions to Authors
Submission of articles
Required Documents
Editorial Responsibilities
Charges Fees
Conflict of interest
Media
Videos
Podcasts
Contact
Home
Past Issues
Summary Vol.70 Issue
2 / 2007
Article
Editorial
Views
Arq. Bras. Oftalmol. 2007; 70 (2):
Total:
2055
Incomplete Vogt-Koyanagi-Harada syndrome associated with HLA DRB1*01 in a 4-year-old child: case report
Related content
Statistics
About the authors
Article
Submission is temporarily unavailable. reCAPTCHA validation has not been configured yet.
Message
Name
E-mail
will not be published
This article not yet has been commented, be the first!
Read in Portuguese
Print
PDF Portuguese
Share
▼
Send this article by email
Submit a comment
Mendeley
Pocket
Share on Facebook
Share on Twitter
Share on Linkedin
Share on WhatsApp
How to cite this article:
Síndrome de Vogt-Koyanagi-Harada incompleta associada a HLA DRB1*01 em criança de quatro anos de idade: relato de caso. Arq. Bras. Oftalmol. 2007;70(2):.
Export citation
ABO is licensed under a Creative Commons Attribution-NonComercial 4.0 Internacional.
