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European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT)

机译：欧洲参考网络用于罕见血管疾病（VASCERNE）脑筛查成人和遗传性出血性毛细血管直学患者脑筛查的立场声明（HHT）

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General Screening Concepts

机译：一般筛选概念

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期刊名称 Orphanet Journal of Rare Diseases
作者
Omer F. Eker; Edoardo Boccardi; Ulrich Sure; Maneesh C. Patel; Saverio Alicante; Ali Alsafi; Nicola Coote; Freya Droege; Olivier Dupuis; Annette Dam Fialla; Bryony Jones; Ujwal Kariholu; Anette D. Kjeldsen; David Lefroy; Gennaro M. Lenato; Hans Jurgen Mager; Guido Manfredi; Troels H. Nielsen; Fabio Pagella; Marco C. Post; Catherine Rennie; Carlo Sabbà; Patrizia Suppressa; Pernille M. Toerring; Sara Ugolini; Elisabetta Buscarini; Sophie Dupuis-Girod; Claire L. Shovlin;
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年(卷),期 2020(-1),-1
年度 2020
页码 -1
总页数 10
原文格式 PDF
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中图分类医学史;
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中文文献

1. European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants [J] . Ingrid M. B. H. van de Laar, Eloisa Arbustini, Bart Loeys, Orphanet journal of rare diseases . 2019,第1期

机译：欧洲罕见血管疾病参考网络（VASCERN）共识性声明，用于筛选和管理具有病原性ACTA2变异的患者
2. Should asymptomatic patients with hereditary haemorrhagic telangiectasia (HHT) be screened for cerebral vascular malformations? Data from 22 061 years of HHT patient life. [J] . Easey AJ, Wallace GM, Hughes JM, Journal of Neurology, Neurosurgery and Psychiatry . 2003,第6期

机译：是否应该筛查无症状的遗传性出血性毛细血管扩张（HHT）患者的脑血管畸形？ HHT患者寿命为22 061年的数据。
3. Screening for pulmonary and cerebral arteriovenous malformations in children with hereditary haemorrhagic telangiectasia. [J] . Al Saleh S, Mei Zahav M, Faughnan ME The European respiratory journal : . 2009,第4期

机译：筛查遗传性出血性毛细血管扩张儿童的肺和脑动静脉畸形。
4. Implementation of EXABO - An Expert Advisory Board for the European Reference Network for Rare Respiratory Diseases [C] . Désirée Walther, Olivia Steinmann, Thomas O.F. Wagner, Medical Informatics Europe Conference . 2020

机译：exabo的实施 - 欧洲参考网络稀有呼吸系统疾病的专家咨询委员会
5. European Reference Network For Rare Vascular Diseases (VASCERN) Outcome Measures For Hereditary Haemorrhagic Telangiectasia (HHT) [O] . Claire L. Shovlin, Elisabetta Buscarini, Anette D. Kjeldsen, 2018

机译：欧洲稀有血管疾病参考网络（VASCERN）遗传性出血性毛细血管扩张（HHT）的结果指标
6. European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT) [O] . Omer F. Eker, Edoardo Boccardi, Ulrich Sure, 2020

机译：欧洲参考网络用于罕见血管疾病（VASCERNE）脑筛查成人和遗传性出血性毛细血管直学患者脑筛查的立场声明（HHT）

European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT)

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