Protocol for the nationwide registry of patients with polycystic kidney disease: japanese national registry of PKD (JRP).
Shinya NakataniHaruna KawanoMai SatoJunichi HoshinoSaori NishioKenichiro MiuraAkinari SekineTatsuya SuwabeSumi HidakaHiroshi KataokaEiji IshikawaKeiji ShimazuKiyotaka UchiyamaTakuya FujimaruTomofumi MoriyamaMahiro KurashigeWataru ShimabukuroFumihiko HattandaTomoki KimuraYusuke UshioShun ManabeHirofumi WatanabeMichihiro MitobeKoichi SetaYosuke ShimadaHirayasu KaiKan KatayamaDaisuke IchikawaHiroki HayashiKazushige HanaokaToshio MochizukiKoichi NakanishiKen TsuchiyaShigeo HorieYoshitaka IsakaSatoru Mutonull nullPublished in: Clinical and experimental nephrology (2024)
The JRP is the first nationwide registry study for patients with ADPKD and ARPKD in Japan, providing researchers with opportunities to advance knowledge and treatments for ADPKD and ARPKD, and to inform disease management and future clinical practice.