Book Chapter
Heritable Disorders of RPE, Bruch’s Membrane, and the Choriocapillaris
Arlene V. Drack
2006, Handbook of Pediatric Retinal Disease, Pages 96-134
Journal Article
Genotype–phenotype correlations and differential diagnosis in autosomal dominant macular disease
Alessandro Iannaccone
Documenta Ophthalmologica, 2001, Volume 102, Number 3, Pages 197-236
Journal Article
Molecular genetics of macular degeneration
Maria A. Musarella
Documenta Ophthalmologica, 2001, Volume 102, Number 3, Pages 165-177
Protocol
Ophthalmologists’ Perspective
Susan M. Downes, N. H. Victor Chong and Alan C. Bird
Methods in Molecular Medicine™, 1, Volume 47, Vision Research Protocols, Pages 251-305
Journal Article
Pattern dystrophies of the retinal pigment epithelium
H. P. Kempeneers, A. Dewachter and G. M. Kempeneers
Documenta Ophthalmologica, 1990, Volume 76, Number 3, Pages 261-272
Journal Article
Detection of retinal dysfunction in vitelliform macular dystrophy using the multifocal ERG (MF-ERG)
Anja M. Palmowski, Reiner Allgayer, Bernhild Heinemann-Vernaleken, Volker Scherer and Klaus W. Ruprecht
Documenta Ophthalmologica, 2003, Volume 106, Number 2, Pages 145-152
Journal Article
Pattern dystrophy of the retinal pigment epithelium with vitelliform macular lesion: evolution in ten years
F. Cardillo Piccolino and M. Zingirian
International Ophthalmology, 1987, Volume 11, Number 4, Pages 207-217
Journal Article
Electroretinographic findings in macular dystrophy
Michael Patrick Clarke, Keith William Mitchell and Sharon McDonnell
Documenta Ophthalmologica, 1996, Volume 92, Number 4, Pages 325-339
Book Chapter
Best’s Disease
2006, Electrodiagnosis of Retinal Diseases, 2, Pages 165-167
Journal Article
Choroidal neovascularisation secondary to Best’s disease in a 13-year-old boy treated by intravitreal bevacizumab
Jörg Leu, Norbert F. Schrage and Robert F. Degenring
Graefe's Archive for Clinical and Experimental Ophthalmology, 2006, Volume 245, Number 11, Pages 1723-1725