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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease pulmonary arterial hypertension
Comorbidity C0005283|beta thalassemia
Sentences 1
PubMedID- 25170276 Objective: the aim of the research reported here was to compare pulmonary artery systolic pressure (pasp) and 6-minute walk distance after 1 year of follow-up in hemoglobin e/beta thalassemia (e/beta-thal) with pulmonary arterial hypertension (pah) patients who received chronic blood transfusions versus those who received occasional transfusions.

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