2017 in Review - 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 of North America
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AKU Society raises £32,000 for Black Bone Disease patient registry
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
Our Eighth AKU Workshop in Memory of Robert Gregory - The AKU Society
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AKU Society raises £32,000 for Black Bone Disease patient registry
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The AKU Society is a patient organisation helping people with the rare genetic disease, Alkaptonuria (AKU). Our we… | Helping people, Rare disease, Genetic diseases
The story of the AKU Society | Webinar Recording | VIA
Support The AKU Society - GCSG - Global Clinical Supplies Group
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Home - The AKU Society
AKU Society - Our key information leaflets about AKU are now available to download in 15 Languages, including عربي, Polskie, Cymraeg and اردو, to name but a few. Visit https://akusociety.org/information-and-support/aku-downloadable-resources/ to check
AKU Society Archives - NORD (National Organization for Rare Disorders)
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Information and Support - The AKU Society
