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Schölvinck, Anne-Floor M.; Pittens, Carina A. C. M.; Broerse, Jacqueline E. W. – Journal of Visual Impairment & Blindness, 2017
Introduction: Despite the relatively high prevalence and challenges of visual impairments, limited funding is available for ophthalmologic research in the Netherlands. The research needs of people with visual impairments could aid the ophthalmological research community to optimally distribute research resources. The objective of the study…
Descriptors: Visual Impairments, Foreign Countries, Ophthalmology, Deaf Blind
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Science Teacher, 2005
Johns Hopkins researchers at the Wilmer Eye Institute have discovered what appears to be the first human gene mutation that causes extreme farsightedness. The researchers report that nanophthalmos, Greek for "dwarf eye," is a rare, potentially blinding disorder caused by an alteration in a gene called MFRP that helps control eye growth and…
Descriptors: Ophthalmology, Visual Impairments, Medical Research, Genetics
Feely, Mary; Vetere, Arlene; Myers, Lynn B. – Journal of Visual Impairment & Blindness, 2007
One of the most prevalent visual impairments of people aged 60 and older is age-related macular degeneration (AMD), which ranks third globally as a cause of visual impairment (World Health Organization, 2006). The purpose of this study was to conduct a tentative subjective assessment of eccentric viewing by persons with AMD. The authors recruited…
Descriptors: Foreign Countries, Partial Vision, Visual Impairments, Qualitative Research
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Science Teacher, 2005
Age-related macular degeneration is the leading cause of blindness in older adults, yet researchers are still in the dark about many of the factors that cause this incurable disease. But new insight from University of Florida (UF) and German researchers about a genetic link between rhesus monkeys with macular degeneration and humans could unlock…
Descriptors: Blindness, Primatology, Medical Research, Ophthalmology
Corwin, Thomas R; Mancini, Michael – 1978
A new test designed to detect an hereditary eye disease called retinitis pigmentosa (RP) is described. This condition is revealed by pigmentation in the retina, but early diagnosis is difficult because the symptoms are subtle, and since it is genetically recessive it frequently occurs in families with no history of early blindness. In many cases…
Descriptors: Eyes, Medical Research, Ophthalmology, Physiology
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Pollard, Zane F. – Pediatrics, 1977
Available from: Arthur Retlaw and Associates, Inc., Suite 2080, 1603 Orrington Avenue, Evanston, Illinois 60201.
Descriptors: Children, Eyes, Medical Evaluation, Medical Research
Patrick, Timothy B.; Sievert, MaryEllen; Reid, John C.; Rice, Frances Ellis; Gigantelli, James W.; Schiffman, Jade S.; Shelton, Mark E. – Proceedings of the ASIST Annual Meeting, 2003
Investigates the shared use of core Ophthalmology terms in the domains of Ophthalmology, Family Practice and Radiology. Core terms were searched for in a text corpus of 38,695 MEDLINE abstracts covering 1970-1999 from journals representing the three domains. Findings indicated core Ophthalmology terms were used significantly more by Ophthalmology…
Descriptors: Abstracts, Family Practice (Medicine), Information Retrieval, Information Seeking
Trutneva, K. – 1972
The booklet describes approaches used in the Union of Soviet Socialist Republics to prevent blindness. It contrasts conditions prior to 1917 (300 eye doctors mainly located in large cities and 2,000 hospital beds for the 300,000 totally blind and 7,000,000 people with trachoma) with conditions in 1971 when in the Ukraine alone there were 3,000 eye…
Descriptors: Delivery Systems, Diseases, Exceptional Child Services, Foreign Countries