European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT)
欧洲罕见血管疾病参考网络 (VASCERN) 关于对患有遗传性出血性毛细血管扩张症 (HHT) 的成人和儿童进行脑部筛查的立场声明
期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-020-01386-9
Eker, Omer F; Boccardi, Edoardo; Sure, Ulrich; Patel, Maneesh C; Alicante, Saverio; Alsafi, Ali; Coote, Nicola; Droege, Freya; Dupuis, Olivier; Fialla, Annette Dam; Jones, Bryony; Kariholu, Ujwal; Kjeldsen, Anette D; Lefroy, David; Lenato, Gennaro M; Mager, Hans Jurgen; Manfredi, Guido; Nielsen, Troels H; Pagella, Fabio; Post, Marco C; Rennie, Catherine; Sabbà, Carlo; Suppressa, Patrizia; Toerring, Pernille M; Ugolini, Sara; Buscarini, Elisabetta; Dupuis-Girod, Sophie; Shovlin, Claire L
