The improvement of pulmonary artery pressure after bosentan therapy in patients with β-thalassemia and Doppler-defined pulmonary arterial hypertension-Reference-Cited by-同舟云学术

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The improvement of pulmonary artery pressure after bosentan therapy in patients with β-thalassemia and Doppler-defined pulmonary arterial hypertension

Published:2018-12 Issue: Volume:Volume 12 Page:1-7
ISSN:1179-142X
Container-title:International Medical Case Reports Journal
language:en
Short-container-title:IMCRJ

Author:

Karami Hossein,Darvishi-Khezri Hadi,Kosaryan Mehrnoush,Akbarzadeh Rosetta,Dabirian Mojdeh

Publisher

Informa UK Limited

Subject

General Medicine

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Group 5 Pulmonary Hypertension: Multiple Systemic Diseases, Multiple Mechanisms of Pulmonary Hypertension, and Multiple Management Challenges;Current Respiratory Medicine Reviews;2024-08

2. Macitentan Administration for Pulmonary Hypertension Due to β-thalassemia with Multiple Organ Failure: A Case Report;Internal Medicine;2024

3. Clinical Complications and Their Management;Hematology/Oncology Clinics of North America;2023-04

4. Pulmonary hypertension in thalassemia: a call to action;Blood;2022-03-31

5. The wide spectrum of β‐thalassaemia intermedia‐induced pulmonary hypertension: two case reports on the possible role of specific pulmonary arterial hypertension therapy;Pulmonary Circulation;2021-07

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