Richard G. Weleber
Oregon Retinal Degeneration Center
Oregon Health & Science University
Portland
USA
Name/email consistency: high
- The phenotype of Severe Early Childhood Onset Retinal Dystrophy (SECORD) from mutation of RPE65 and differentiation from Leber congenital amaurosis. Weleber, R.G., Michaelides, M., Trzupek, K.M., Stover, N.B., Stone, E.M. Invest. Ophthalmol. Vis. Sci. (2011)
- Clinical and electrophysiologic characterization of paraneoplastic and autoimmune retinopathies associated with antienolase antibodies. Weleber, R.G., Watzke, R.C., Shults, W.T., Trzupek, K.M., Heckenlively, J.R., Egan, R.A., Adamus, G. Am. J. Ophthalmol. (2005)
- Electroretinographic and clinicopathologic correlations of retinal dysfunction in infantile neuronal ceroid lipofuscinosis (infantile Batten disease). Weleber, R.G., Gupta, N., Trzupek, K.M., Wepner, M.S., Kurz, D.E., Milam, A.H. Mol. Genet. Metab. (2004)
- Treatment of retinal and choroidal degenerations and dystrophies: current status and prospects for gene-based therapy. Weleber, R.G., Kurz, D.E., Trzupek, K.M. Ophthalmol. Clin. North. Am (2003)
- Infantile and childhood retinal blindness: a molecular perspective (The Franceschetti Lecture). Weleber, R.G. Ophthalmic Genet. (2002)
- The dystrophic retina in multisystem disorders: the electroretinogram in neuronal ceroid lipofuscinoses. Weleber, R.G. Eye. (Lond) (1998)
- X-linked retinitis pigmentosa associated with a 2-base pair insertion in codon 99 of the RP3 gene RPGR. Weleber, R.G., Butler, N.S., Murphey, W.H., Sheffield, V.C., Stone, E.M. Arch. Ophthalmol. (1997)