RobertTWoodburnIIIMD

PubMed

• 5 citations
  The A‐1 antigen: A novel marker in experimental peripheral nerve injury
  Biagio Azzarelli, Robert Woodburn, Suman Olivelle, Sean Kimbro, Aristotle N. Siakotos
  The Journal of Comparative Neurology. 1993-11-15
• 3 citations
  Cerebrovascular accident with unusual electrocardiographic changes.
  Gary J. Anderson, Robert Woodburn, Charles Fisch
  American Heart Journal. 1973-09-01
• 3 citations
  Advances in gynecologic radiation oncology.
  Robert Woodburn, Marcus E. Randall
  Current Opinion in Oncology. 1997-09-01

Abstracts/Posters

• The Role of Project Sponsors in an Interprofessional Quality Improvement Curriculum for Internal Medicine Residents and Masters of Public Health Students.
  Sloan, K., Gupte, G., Suen, W., Sloan, K., Noronha, C, Association of American Medical Colleges Integrating Quality Meeting: Increasing Value and Educating for Quality, Rosemont, IL, 1/1/2013
• Transcription activator-like effector nuclease-based genome editing for mucopolysaccharidosis Type I.
  Osborn MJ, Starker CG, DeFeo AP, Voytas DF, Blazar BR, Tolar J, Mol Ther; American Society of Cell and Gene Therapy, Salt Lake City, UT, 1/1/2013
• Chitotriosidase as a biomarker of cerebral adrenoleukodystrophy.
  Orchard PJ, Basso L, Kivisto T, Raymond G, Charnas L, Lund TC, Tolar J, Mol Genet Metabol; Lysosomal Disease Network's WORLD Symposium, Miami, FL, 1/1/2010
• Patient-specific induced pluripotent stem cells in mucopolysaccharidosis type I.
  Tolar J, Park IH, Xia L, Osborn MJ, Lund T, Orchard PJ, Daley GQ, Blazar BR, Lysosomal Disease Network/WORLD Symposium, Miami, FL, 1/1/2010
• CNS-specific FGFR3 K644E transgenic mice: gene expression profile [abstract 1042].
  Lin T, Sandusky SB, Xue H, Heitman AM, Rao MS, Francomano CA, Annual Meeting of The American Society of Human Genetics, Toronto, Canada, 1/1/2004
• A study of linkage of anthropometric traits related to obesity in the Old-Order Amish [abstract 2028].
  Papanicolaou GJ, Platte P, Klein CM, Doheny KF, Roy-Gagnon MH, Stunkard AJ, Francomano CA, Wilson AF, Annual Meeting of The American Society of Human Genetics, Toronto, Canada, 1/1/2004
• A nonsense mutation induces skipping of a constitutive fibrillin (FBN1) exon in vivo in a patient with Marfan syndrome.
  Dietz HC, Kendzior RJ, Francomano CA, Pyeritz RE, and Cutting GR, Second International Symposium on the Marfan Syndrome, San Francisco, CA, 1/1/1992
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Lectures

• Reaching for the Stars: The Promise of Stem Cells and the Future of Regenerative Medicine 
  Plymouth - 1/1/2014
• Bench to Bedside 
  Minneapolis, MN - 1/11/2011
• Comparative Analyses of the Retinal Degenerations in Usher Syndromes (USH) 
  Miami, FL - 1/1/2008