EURORDIS Members Award 2020 - EURORDIS Black Pearl Awards
Home - The AKU Society
Home - The AKU Society
2021 Online Mini Workshop - Round Up - The AKU Society
The Challenges of Alkaptonuria, a Rare Disease – written by AKU Society | One Nucleus Blog
Rare Revolution
The Alkaptonuria Society - JustGiving
Cambridge-based AKU Society in BBC Radio 4 fundraising appeal
AKU Society launches crowdfunding campaign for Black Bone Disease – EJP RD – European Joint Programme on Rare Diseases
The New AKU Society Website - The AKU Society
AKU Society upcoming events in Winter 2019 - The AKU Society
AKU Society on Twitter: "Our #CrowdfundingCampaign launches tomorrow at 2 pm GMT. Stay tuned for more updates soon. Hear from one of our hardworking volunteers about her #AKU story and why the
Support The AKU Society - GCSG - Global Clinical Supplies Group
Cure Black Bone Disease: Time Is Running Out | Indiegogo
The story of the AKU Society | Webinar Recording | VIA
Liverpool researchers find treatment for ultra-rare disease - News - University of Liverpool
Tweets with replies by AKU Society (@AKUSociety) / Twitter
AKU Society - AKU Society updated their cover photo.
Healx pledges $25,000 to AKU Society patient registry campaign - Healx
Tweets with replies by AKU Society (@AKUSociety) / Twitter
New AKU treatment comes closer to commercialisation | Interview | CORDIS | European Commission