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New promise for glaucoma treatment

Iowa State University researchers have developed a new technique that successfully treated rats for blindness caused by glaucoma. Their experimental treatment will be used on canine patients in the next year. If successful, it is expected to move to human trials.

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Fish eyes to help to repairing damaged retinas in humans

A special type of cell found in the eye has been found to be very important in regenerating the retina in zebrafish and restoring vision even after extensive damage. Now, a UK team of scientists believe they may be able to use these cells – known as Müller glial cells – to regenerate damaged retina in humans, according to a study published this month in the journal Stem Cells.

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New gene therapy tools for inherited blindness

An improved approach to gene therapy may one day treat some of the nearly 200 inherited forms of blindness, scientists at Washington University School of Medicine in St. Louis suggest this week.

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Drivers warned of undiagnosed glaucoma

An organisation representing people with eye diseases is warning that more than 100,000 people could be driving with partial blindness and not know it.

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Karen Avraham leads groundbreaking effort to understand deafness in children

Prof. Karen Avraham, chair of the department of human molecular genetics and biochemistry at Tel Aviv University’s Sackler School of Medicine, represented EuroHear, a consortium of 25 European, Israeli and U.K.-based research teams, at the European Union conference “Hearing and Seeing: European Research to Fight Deafness and Blindness,” held at Paris’s College de France on July 2-3, 2007.

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View on new drugs for macular degeneration

Restricting use of drugs for macular degeneration to patients who have already gone blind in one eye is “unacceptable” concludes the July issue of Drug and Therapeutics Bulletin (DTB).

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Blind Kids Follow the Dots to Success

America's top blind students prepare to compete in unique academic competition.

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Study Maps Road to Cure for Inherited Eye Diseases

Researchers at the University of Pennsylvania School of Medicine have identified proteins in the rod and cones of the eye that could lead to the discovery of the genetic causes of a host of inherited eye diseases. The investigators hope to gain a clearer understanding of what goes wrong at the most basic level in these diseases that cause blindness and other disorders.

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Blind people are 'serial memory' whizzes

Compared to people with normal vision, those who were blind at birth tend to have excellent memories. Now, a new study reported online on June 21st in the journal Current Biology, a publication of Cell Press, shows that blind individuals are particular whizzes when it comes to remembering things in the right order.

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Nanoparticle Offers Promise for Treating Glaucoma

A unique nanoparticle made in a laboratory at the University of Central Florida is proving promising as a drug delivery device for treating glaucoma, an eye disease that can cause blindness and affects millions of people worldwide.

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Smart Card Based e-Security to the Blind and Visually Impaired

Accessibility of Internet Applications Boosted by VASCO's Digipass Comfort Voice Range; Seamless Support by VACMAN Controller Makes Digipass 840 CV Compatible with the Entire Digipass Product Range

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New gene discovery offers further hope for childhood blindness

An international research team has discovered a gene that, when mutated, causes one of the most common forms of inherited blindness in babies. Scientists at the University of Leeds, working in collaboration with experts from other centres around the world, identified the gene, which is essential to photoreceptors in the eye, the cells that "see" light.

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