5 May 2021 | AE, News & Events
Aniridia Europe is glad to announce a great new partnership with Aniridia-Net in order to promote knowledge on Aniridia and updates on its treatments. Starting from May 26th at 6:00 PM CEST, in fact, Aniridia Europe and Aniridia-net will implement a series of monthly...
25 April 2021 | AE, National activities, News & Events
In Italy, a group of young adults with aniridia decided to do something more for their friends. In June 2020 they built a team composed by 4 young ladies and 2 young men who began to publish posts on social networks, creating funny digital events, promoting and...
20 April 2021 | AE, News & Events
Since Covid-19 spread out at global level, governments and institutions have set social distancing measures in order to contain the sanitary emergency. Starting from that moment a lot of patients around the world have lost the opportunity to meet face-to-face and to...
27 February 2021 | AE, News & Events
For the Rare Disease Week 2021 Aniridia Europe organized the webinar “News from the frontier” about the Aniridia-Net COST Action and the latest news about aniridia treatment and research. The webinar started with a welcome speech by Ivana Kildsgaard, chairperson of...
23 February 2021 | AE, News & Events
For the Rare Disease Week this year we have organised a webinar about the Aniridia-Net COST Action and the latest news in aniridia treatment and research. Our keynote speakers are dr. Neil Lagali (University of Linköping, Sweden) and dr. Claus Cursiefen (University of...
22 January 2021 | AE, National activities, News & Events
The next European Aniridia Conference will be held online and perhaps in London too, 30 July to 1 August 2021. Make a note in your calendar now and pass this invitation on to anyone who might be interested The event is aimed at professionals, patients and parents. As...
