Meet a Researcher: Tomasz Tomkiewicz
Tomasz Tomkiewicz is undertaking a PhD studentship funded by Retina UK and The Macular Society.
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Tomasz Tomkiewicz is undertaking a PhD studentship funded by Retina UK and The Macular Society.
Choroideremia is a rare genetic condition resulting in progressive sight loss in men.
Autoimmune diseases are quite distinct from inherited retinal dystrophies.
The FDA has given Ocugen permission to start their phase 3 gene therapy clinical trial for retinitis pigmentosa (RP).
Inherited retinal dystrophies (IRDs) are the leading cause of blindness in working-age people in the UK, and children as young as eighteen-months are regularly diagnosed.
After more than 10 years of service as Chair of the Board of Trustees, Don Grocott has retired.
Research determines that taking high dose vitamin A supplements does not slow vision loss in people with retinitis pigmentosa (RP).
We are proud to work collaboratively with a number of corporate partners to enable our community to live fulfilled lives today as well as supporting the pharmaceutical industry in their mission to develop potential new treatments.
This page explains the different types of genetic tests: diagnostic testing, predictive testing, carrier testing and research testing
Retina UK aims not only to progress research along established threads, but to stimulate new thinking, encourage innovative approaches and nurture original ideas.