Clinical indicators for pulmonary arterial hypertension in thalassemia

• المؤلفون الرئيسيون: Chueamuangphan N., Wongtheptien W., Nawarawong W., Sukornthasarn A., Chuncharunee S., Tawichasri C., Patumanond J.
• التنسيق: مقال
• اللغة: English
• منشور في: 2014
• الوصول للمادة أونلاين: http://www.scopus.com/inward/record.url?eid=2-s2.0-84856870900&partnerID=40&md5=cc95cdf0499fdcd0d280c176c851f12d; http://cmuir.cmu.ac.th/handle/6653943832/3938

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...