Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Rod W. Nowakowski"'
Autor:
Gary Mancil, Ellis King, Bruce B. Blasch, Claudine Legault, Rickilyn Mancil, Julie Munday, Rod W. Nowakowski, Salvatore Alfieri
Publikováno v:
Journal of rehabilitation research and development. 42(4)
This study compared the effectiveness of the ITT Night Vision Viewer with the Wide Angle Mobility Lamp (WAML) as low-vision mobility devices for people experiencing night blindness due to retinitis pigmentosa (RP). Both engineering bench testing and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57f662379300012caeb0be55e2416b32
https://pubmed.ncbi.nlm.nih.gov/16320143
https://pubmed.ncbi.nlm.nih.gov/16320143
Autor:
Joseph Wagstaff, Athel Hockey, Paul J. Benke, De-Ann M. Pillers, Mildred L. Kistenmacher, Seth J. Orlow, Arthur W. Grix, Rhonda E. Schnur, Graham E. Quinn, Roberta S. Pagon, Matthew S. Edwards, Hope H. Punnett, Maria A. Musarella, Mei Gao, Kenneth K. Kidd, Kamer Tezcan, Margaret Keller, Alex V. Levin, Jack H. Jung, Richard G. Weleber, Rod W. Nowakowski, Richard A. Lewis, Penelope A. Wick
X-linked ocular albinism (OA1), Nettleship-Falls type, is characterized by decreased ocular pigmentation, foveal hypoplasia, nystagmus, photodysphoria, and reduced visual acuity. Affected males usually demonstrate melanin macroglobules on skin biopsy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6077cec5275bd5903184dd097b91624f
https://europepmc.org/articles/PMC1377018/
https://europepmc.org/articles/PMC1377018/
Autor:
Rod W. Nowakowski
Publikováno v:
Optometry and Vision Science. 61:643-646
De nombreuses anomalies liees au chromosome X sont localisees a l'œil ou ont des manifestations oculaires. Les conseils genetiques aux porteurs potentiels demandent une estimation fiable du risque. L'article donne une application du theoreme de Baye
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6cf6cb11672800a81f708da3f372318d
https://doi.org/10.1097/00006324-198410000-00004
https://doi.org/10.1097/00006324-198410000-00004
Publikováno v:
Pediatric Research. 26:462-466
Sanfilippo syndrome, type D (MPS IIID), is characterized by moderate physical abnormalities, pro- gressive mental deterioration, and deficient activity of N- acetylglucosamine 6-sulfate sulfatase, a lysosomal hydro- lase involved in the degradation o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e15309517fdf1dd9c769af1ad910a6de
https://doi.org/10.1203/00006450-198911000-00020
https://doi.org/10.1203/00006450-198911000-00020
Publikováno v:
Optometry and Vision Science. 65:209-211
Leber optic atrophy (LOA) is a familial disorder primarily affecting males. We report the case of a 44-year-old male for whom the prescription of low vision aids was an important rehabilitative factor.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2db30e5f0f06bc6ce5ac8d3d68379746
https://doi.org/10.1097/00006324-198803000-00010
https://doi.org/10.1097/00006324-198803000-00010
Autor:
Gary L. Mancil, Rod W. Nowakowski
Publikováno v:
American journal of optometry and physiological optics. 63(9)
Four commonly prescribed low vision aids of equivalent power were evaluated to determine maximum reading speed of normally sighted young adults. Subjects tested were fully sighted and of similar educational backgrounds. Presentation of the four aids
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5895820669d4eebf2219e188fb73614
https://pubmed.ncbi.nlm.nih.gov/3777120
https://pubmed.ncbi.nlm.nih.gov/3777120