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See Latest ArticlesPulmonary Hypertension in Grave's Disease
The Endocrinologist, 11/18/08
Haran M et al. - Pulmonary arterial hypertension (PAH) is characterized by pulmonary artery systolic pressure (PASP) >35 mm Hg or mean >30 mm Hg with exercise. Etiology is divided into primary or secondary causes.
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