Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY010539-03
Application #
2164462
Study Section
Visual Sciences C Study Section (VISC)
Project Start
1994-06-01
Project End
1999-05-31
Budget Start
1996-06-01
Budget End
1997-05-31
Support Year
3
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of Iowa
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Drack, Arlene V; Lambert, Scott R; Stone, Edwin M (2010) From the laboratory to the clinic: molecular genetic testing in pediatric ophthalmology. Am J Ophthalmol 149:10-17
Ghodasra, Devon H; Nallasamy, Sudha; Binenbaum, Gil (2009) Congenital trigemino-abducens synkinesis in a neonate. J AAPOS 13:417-8
Drack, Arlene V; Johnston, Rebecca; Stone, Edwin M (2009) Which Leber congenital amaurosis patients are eligible for gene therapy trials? J AAPOS 13:463-5
Thompson, Stewart; Foster, Russell G; Stone, Edwin M et al. (2008) Classical and melanopsin photoreception in irradiance detection: negative masking of locomotor activity by light. Eur J Neurosci 27:1973-9
Forbes, Brian J; Katowitz, William R; Binenbaum, Gil (2008) Pediatric canalicular tear repairs--revisiting the pigtail probe. J AAPOS 12:518-20
Kang Derwent, Jennifer J; Derlacki, Deborah J; Hetling, John R et al. (2004) Dark adaptation of rod photoreceptors in normal subjects, and in patients with Stargardt disease and an ABCA4 mutation. Invest Ophthalmol Vis Sci 45:2447-56
Oh, Kean T; Weleber, Richard G; Oh, Dawn M et al. (2004) Clinical phenotype as a prognostic factor in Stargardt disease. Retina 24:254-62
Oh, Kean T; Weleber, Richard G; Stone, Edwin M et al. (2004) Electroretinographic findings in patients with Stargardt disease and fundus flavimaculatus. Retina 24:920-8
Kuehn, M H; Stone, E M; Hageman, G S (2001) Organization of the human IMPG2 gene and its evaluation as a candidate gene in age-related macular degeneration and other retinal degenerative disorders. Invest Ophthalmol Vis Sci 42:3123-9
Donoso, L A; Frost, A T; Stone, E M et al. (2001) Autosomal dominant Stargardt-like macular dystrophy: founder effect and reassessment of genetic heterogeneity. Arch Ophthalmol 119:564-70

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