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Read about PKD research and other research relevant to PKD.
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Volunteers are needed to participate in a clinical research trial for Pediatric Patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD).
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If you have ADPKD (Autosomal Dominant Polycystic Kidney Disease) or ARPKD (Autosomal Recessive Polycystic Kidney Disease), you may be eligible to take part in the 100,000 Genomes Project run by Genomics England, part of the Department of Health.
You may have heard of this exciting project in the media. Genomics England is analysing - known as 'sequencing' - 100,000 genomes of people in the UK with rare diseases and cancer. The aim is to stimulate innovative research, deliver greater medical insights and transform genetics health services. Some people may also receive a conclusive diagnosis for the first time.
RT @JeremyCraneMD: So excited to be curating the @NHS twitter handle next week - lots to talk about! The last guy @drilanbz did pretty well…
Good luck! @plrh_cambridge: hard at work on TWO new, very exciting grant applications for proposals from @gitelmansuk @PKDCharity patients!
RT @phil_thornton: As an ADPKD patient, this is fantastic news for South Tyneside ~ Kidney experts appointed at South Tyneside hospital htt…
RT @cansolveckd: “Everyone was here to understand everyone else’s perspective”: Mike McCormick reflects on @cansolveckd partnership https:/…
RT @scotorgandonor: Airdrie mum who received life-saving transplant urges others to join Organ Donor Register https://t.co/SUra3DOdtp https…
RT @JeremyCraneMD: So excited to be curating the @NHS twitter handle next week - lots to talk about! The last guy @drilanbz did pretty well…
