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Early-life pulmonary arterial hypertension with subsequent development of diffuse pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia type 1

机译：早期肺动脉高血压随后发育遗传性肺病性血管血管直学患者的弥漫性肺动脉畸形

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C J Mache; A Gamillscheg; H H Popper; S G Haworth;
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1. Early-life pulmonary arterial hypertension with subsequent development of diffuse pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia type 1. [J] . Mache CJ, Gamillscheg A, Popper HH, Thorax: The Journal of the British Thoracic Society . 2008,第1期

机译：早期生命型肺动脉高压，随后发展为1型遗传性出血性毛细血管扩张的弥漫性肺动静脉畸形。
2. PATIENTS WITH PULMONARY ARTERIOVENOUS MALFORMATIONS AND HEREDITARY HAEMORRHAGIC TELANGIECTASIA REPORT FORCED EXPIRATORY MANOEUVRES DURING PULMONARY FUNCTION TESTS PROVOKE NOSEBLEEDS AND MIGRAINES [J] . Tighe H. C., McKernan H., Springett J. T., Thorax: The Journal of the British Thoracic Society . 2016,第Suppla3期

机译：肺功能异常和遗传性出血性肾小球性肾炎的患者报告在进行肺功能测试期间强制进行呼气动作，引起不必要和偏头痛
3. Endovascular sampling of endothelial cells from pulmonary arteriovenous malformations in hereditary hemorrhagic telangiectasia: a new methodology for elucidating the molecular mechanisms underlying arteriovenous malformation development [J] . McGregor Hugh, Cooke Daniel, Sun Zhengda, Angiogenesis . 2015,第4期

机译：从遗传性出血性毛细血管扩张中的肺动静脉畸形内皮细胞的血管内采样：阐明动静脉畸形发展的分子机制的一种新方法。
4. Automatic detection and quantification of pulmonary arterio-venous malformations in hereditary hemorrhagic telangiectasia [C] . Catalin Fetita, Thierry Fortemps de Loneux, Amele Florence Kouvahe, Conference on Computer-Aided Diagnosis . 2017

机译：遗传性出血性毛细血管扩张症中肺动静脉畸形的自动检测和定量
5. Genotypic/phenotypic analysis of endothelial progenitor cells in idiopathic pulmonary arterial hypertension and hereditary hemorrhagic telangiectasia [D] . Zucco, Liana V. 2006

机译：特发性肺动脉高压和遗传性出血性毛细血管扩张症中内皮祖细胞的基因型/表型分析
6. Severe pulmonary hypertension associated with hepatic arteriovenous malformation in a patient with hereditary haemorrhagic telangiectasia [O] . Sakolwat Montrivade, Patinya Maneesow, Thamonwan Osotthanakorn, 2018

机译：患有遗传性出血性毛细管扩诊患者的患者肝动脉畸形相关的严重肺动脉高血压
7. P33 Patients with pulmonary arteriovenous malformations and hereditary haemorrhagic telangiectasia report forced expiratory manoeuvres during pulmonary function tests provoke nosebleeds and migraines [O] . HC Tighe, H McKernan, JT Springett, 2016

机译：P33患有肺动脉畸形和遗传性出血性疾病患者报告肺功能试验期间的强迫呼气式动作，挑衅流鼻血和偏头痛

Early-life pulmonary arterial hypertension with subsequent development of diffuse pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia type 1

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