The clinical characteristics and long-term prognosis of pulmonary arterial hypertension associated with hereditary hemorrhagic telangiectasia

Pulmonary arterial hypertension (PAH) is a severe complication of hereditary hemorrhagic telangiectasia (HHT); however, little is known about its clinical characteristics and prognosis. Nine newly diagnosed HHT-PAH patients were prospectively recruited between October 2007 and January 2016 and were...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Wen, Xiong, Chang-ming, Gu, Qing, Wang, Xiao-tong, Cheng, Xiao-ling, Huang, Li, Yang, Tao, Luo, Qin, Zhao, Zhi-hui, Ni, Xin-hai, Liu, Zhi-hong, He, Jian-guo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5888830/
https://www.ncbi.nlm.nih.gov/pubmed/29480092
http://dx.doi.org/10.1177/2045894018759918

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5888830/
https://www.ncbi.nlm.nih.gov/pubmed/29480092
http://dx.doi.org/10.1177/2045894018759918

Ejemplares similares