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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Richard G. Weleber

Oregon Retinal Degeneration Center

Oregon Health & Science University

Portland

USA

[email]@ohsu.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Oregon Retinal Degeneration Center, Oregon Health & Science University, Portland, USA. 1997 - 2011
  • Casey Eye Institute, Department of Ophthalmology, Oregon Health & Science University, 3375 Southwest Terwilliger Boulevard, USA. 2003 - 2005
  • Oregon Health Sciences University, Casey Eye Institute, Portland 97201-4197, USA. 1998

References

  1. 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) [Pubmed]
  2. 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) [Pubmed]
  3. 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) [Pubmed]
  4. 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) [Pubmed]
  5. Infantile and childhood retinal blindness: a molecular perspective (The Franceschetti Lecture). Weleber, R.G. Ophthalmic Genet. (2002) [Pubmed]
  6. The dystrophic retina in multisystem disorders: the electroretinogram in neuronal ceroid lipofuscinoses. Weleber, R.G. Eye. (Lond) (1998) [Pubmed]
  7. 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) [Pubmed]
 
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