Janet Priscilla Szlyk
Affiliations: | 1989-1992 | Ophthalmology | University of Illinois at Chicago, Chicago, IL, United States |
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"Janet Szlyk"Mean distance: 17.98 (cluster 23) | S | N | B | C | P |
Parents
Sign in to add mentor| Kenneth Ross Alexander | post-doc | 1989-1992 | University of Illinois, Chicago |
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Publications
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| Grant P, Maeng M, Arango T, et al. (2018) Performance of Real-world Functional Tasks Using an Updated Oral Electronic Vision Device in Persons Blinded by Trauma. Optometry and Vision Science : Official Publication of the American Academy of Optometry. 95: 766-773 |
| Ming J, Thulborn KR, Szlyk JP. (2012) Reproducibility of activation maps for longitudinal studies of visual function by functional magnetic resonance imaging. Investigative Ophthalmology & Visual Science. 53: 6153-63 |
| Grant P, Seiple W, Szlyk JP. (2011) Effect of depression on actual and perceived effects of reading rehabilitation for people with central vision loss. Journal of Rehabilitation Research and Development. 48: 1101-8 |
| Szlyk JP, Little DM. (2009) An FMRI study of word-level recognition and processing in patients with age-related macular degeneration. Investigative Ophthalmology & Visual Science. 50: 4487-95 |
| Soong GP, Shapiro M, Seiple W, et al. (2008) Macular structure and vision of patients with macular heterotopia secondary to retinopathy of prematurity. Retina (Philadelphia, Pa.). 28: 1111-6 |
| Little DM, Thulborn KR, Szlyk JP. (2008) An FMRI study of saccadic and smooth-pursuit eye movement control in patients with age-related macular degeneration. Investigative Ophthalmology & Visual Science. 49: 1728-35 |
| Vajaranant TS, Fishman GA, Szlyk JP, et al. (2008) Detection of mosaic retinal dysfunction in choroideremia carriers electroretinographic and psychophysical testing. Ophthalmology. 115: 723-9 |
| Kim LS, Fishman GA, Seiple WH, et al. (2007) Retinal dysfunction in carriers of bardet-biedl syndrome. Ophthalmic Genetics. 28: 163-8 |
| Kim LS, Seiple W, Fishman GA, et al. (2007) Multifocal ERG findings in carriers of X-linked retinoschisis. Documenta Ophthalmologica. Advances in Ophthalmology. 114: 21-6 |
| Yzer S, Fishman GA, Racine J, et al. (2006) CRB1 heterozygotes with regional retinal dysfunction: implications for genetic testing of leber congenital amaurosis. Investigative Ophthalmology & Visual Science. 47: 3736-44 |