2017 in Review - The AKU Society
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Overview of the number of patients with alkaptonuria reported... | Download Scientific Diagram
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How the AKU Society recruited 50% of their patient population in 9 months
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Jobs with AKU SOCIETY | CharityJob
Our Eighth AKU Workshop in Memory of Robert Gregory - The AKU Society
AKU Society - Last night the AKU Society received the EURORDIS - European Rare Diseases Organisation Members Award at the Black Pearl Awards 2021 We have finally achieved what we set out
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AKU Society raises £32,000 for Black Bone Disease patient registry
The AKU Society is a patient organisation helping people with the rare genetic disease, Alkaptonuria (AKU). Our we… | Helping people, Rare disease, Genetic diseases
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AKU Society - This week's blog is a sad one for us. We are saying goodbye to Juliet, our Head of Fundraising. We wish Juliet the best of luck as she is
10 years of life changing National Alkaptonuria Centre | Genetic Alliance UK
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AKU Society on Twitter: "Would you know if you or your child had #BlackBoneDisease? Our infographic gives the symptoms #AKU #Alkaptonuria http://t.co/xJ2fguQqqn" / Twitter
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AKU Society raises £32,000 for Black Bone Disease patient registry
