Chapter 254 Canine Retinopathies
- Acland GM et al: Gene therapy restores vision in a canine model of childhood blindness, Nat Genet 28:92, 2001. PUBMED Abstract
- Gearhart PM, Gearhart CC, Petersen-Jones SM: A novel method for objective vision testing in canine models of inherited retinal disease, Invest Ophthalmol Vis Sci 49:3568, 2008. PUBMED Abstract
- Guziewicz KE et al: Bestrophin gene mutations cause canine multifocal retinopathy: a novel animal model for best disease, Invest Ophthalmol Vis Sci 48:1959, 2007. PUBMED Abstract
- Hurn SD, Hardman C, Stanley RG: Day-blindness in three dogs: clinical and electroretinographic findings, Vet Ophthalmol 6:127, 2003. PUBMED Abstract
- Komaromy AM et al: Gene therapy rescues cone function in congenital achromatopsia, Hum Mol Genet 19:2581, 2010. PUBMED Abstract
- Landry MP, Herring IP, Panciera DL: Funduscopic findings following cataract extraction by means of phacoemulsification in diabetic dogs: 52 cases (1993-2003), J Am Vet Med Assoc 225:709, 2004. PUBMED Abstract
- McLellan GJ et al: Clinical and pathological observations in English cocker spaniels with primary metabolic vitamin E deficiency and retinal pigment epithelial dystrophy, Vet Rec 153:287, 2003. PUBMED Abstract
- Tao W et al: Encapsulated cell-based delivery of CNTF reduces photoreceptor degeneration in animal models of retinitis pigmentosa, Invest Ophthalmol Vis Sci 43:3292, 2002. PUBMED Abstract
- Wrigstad A, Narfström K, Nilsson SE: Slowly progressive changes of the retina and retinal pigment epithelium in Briard dogs with hereditary retinal dystrophy. A morphological study, Doc Ophthalmol 87:337, 1994. PUBMED Abstract
- Zangerl B et al: Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humans, Genomics 88:551, 2006. PUBMED Abstract
- Zangerl B et al: Assessment of canine BEST1 variations identifies new mutations and establishes an independent bestrophinopathy model (cmr3), Mol Vis 16:2791, 2010. PUBMED Abstract