Correlation between SD-OCT, immunocytochemistry and functional findings in a pigmented animal model of retinal degeneration

• Principais autores: Nicolás eCuenca (Autor), Laura eFernandez-Sanchez (Autor), Yves eSauvé (Autor), Francisco Javier Segura (Autor), Gema Concepcion Martínez-Navarrete (Autor), Jose Manuel Tamarit (Autor), Lorena eFuentes-Broto (Autor), Ana eSanchez-Cano (Autor), Isabel ePinilla (Autor)
• Formato: Livro
• Publicado em: Frontiers Media S.A., 2014-12-01T00:00:00Z.
• Assuntos: article
• Acesso em linha: Connect to this object online.

Purpose: The P23H rhodopsin mutation is an autosomal dominant cause of retinitis pigmentosa. The degeneration can be tracked using different anatomical and functional methods. In our case, we evaluated the anatomical changes using Spectral-Domain Optical Coherence Tomography (SD-OCT) and correlated...