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We want to improve the lives of everyone affected by polycystic kidney disease. But we need your help to do it.
There are many ways you can support our work by donating or raising funds for the PKD Charity.
RT @RenalRadar: The RaDaR rare disease registry and NURTuRE biobank have just reached a landmark recruitment figure... @kidneycareuk @Kidne…
ePAG members in Heidelberg for @EuRefNetwork meeting. https://t.co/Ntp80e5irx
RT @AsgariElham: Prof Bruce Henry on the potential use of antisense in ADPKD #RSMKidneyRD @RoySocMed https://t.co/fhhEWW3LhB
RT @MattLanktree: #ADPKD getting some prime time coverage #endPKD https://t.co/OYi4kHiJVy
RT @AliMehdiMD: ADPKD is actually a “molecular recessive disease”. Cystic tubules have mutations on both alleles as opposed to tubular cell…
RT @RenalRadar: The RaDaR rare disease registry and NURTuRE biobank have just reached a landmark recruitment figure... @kidneycareuk @Kidne…
