Clinical indicators for pulmonary arterial hypertension in thalassemia

• المؤلفون الرئيسيون: Nonlawan Chueamuangphan, Wattana Wongtheptien, Weerasak Nawarawong, Apichard Sukornthasarn, Suporn Chuncharunee, Chamaiporn Tawichasri, Jayanton Patumanond
• التنسيق: دورية
• منشور في: 2018
• الموضوعات: Medicine
• الوصول للمادة أونلاين: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84856870900&origin=inward; http://cmuir.cmu.ac.th/jspui/handle/6653943832/51966

Objective: To explore clinical indicators for pulmonary arterial hypertension (PAH) in thalassemia (Thal). Material and Method: A study was conducted in thalassemia patients at Chiang Rai Hospital, Chiang Rai, Thailand. Pulmonary artery systolic pressure (PASP) was determined by doppler echocardiogr...