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- [31] European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT)Orphanet Journal of Rare Diseases, 15Omer F. EkerEdoardo BoccardiUlrich SureManeesh C. PatelSaverio AlicanteAli AlsafiNicola CooteFreya DroegeOlivier DupuisAnnette Dam FiallaBryony JonesUjwal KariholuAnette D. KjeldsenDavid LefroyGennaro M. LenatoHans Jurgen MagerGuido ManfrediTroels H. NielsenFabio PagellaMarco C. PostCatherine RennieCarlo SabbàPatrizia SuppressaPernille M. ToerringSara UgoliniElisabetta BuscariniSophie Dupuis-GirodClaire L. Shovlin
- [32] Description and Cross-Sectional Analyses of 25,880 Adults and Children in the UK National Registry of Rare Kidney Diseases CohortKIDNEY INTERNATIONAL REPORTS, 2024, 9 (07): : 2067 - 2083Wong, KatiePitcher, DavidBraddon, FionaDownward, LewisSteenkamp, RethaMasoud, SherryAnnear, NicholasBarratt, JonathanBingham, CoralieCoward, Richard J.Chrysochou, TinaGame, DavidGriffin, SianHall, MattJohnson, SallyKanigicherla, DurgaFrankl, Fiona KaretKavanagh, DavidKerecuk, LarissaMaher, Eamonn R.Moochhala, ShabbirPinney, JennySayer, John A.Simms, RoslynSinha, SmeetaSrivastava, ShalabhTam, Frederick W. K.Thomas, KayTurner, A. NeilWalsh, Stephen B.Waters, AoifeWilson, PatriciaWong, EdwinSy, Karla Therese L.Huang, KuiYe, JamieNitsch, DorotheaSaleem, MoinBockenhauer, DetlefBramham, KateGale, Daniel P.