PedAM
Pediatric Disease Annotations & Medicines
| Disease | pulmonary hypertension |
| Phenotype | C1619734|pulmonary arterial hypertension |
| Sentences | 6 |
| PubMedID- 22086457 | Background: candidates for orthotopic liver transplantation (olt) often have porto-pulmonary hypertension (pphtn) with pulmonary arterial hypertension (pah). |
| PubMedID- 20677289 | pulmonary arterial hypertension (pah) associated with portal hypertension [portopulmonary hypertension (pphtn)] occurs in 2% to 10% of patients with advanced liver disease and carries a very poor prognosis without treatment. |
| PubMedID- 22059182 | Assessing response to therapy in idiopathic pulmonary arterial hypertension: a consensus survey of canadian pulmonary hypertension physicians. |
| PubMedID- 25223406 | pulmonary hypertension, including pulmonary arterial hypertension (pah), is a serious disease in children, but few clinical studies have been conducted to evaluate treatment regimens in this population. |
| PubMedID- 26407098 | Background: pulmonary arterial hypertension (pah) is one of several forms of pulmonary hypertension: a chronic disease of the pulmonary vasculature. |
| PubMedID- 23319544 | Chronic exposure to cold caused pulmonary arterial hypertension (cold-induced pulmonary hypertension [ciph]) and increased phosphodiesterase-1c (pde-1c) expression in pulmonary arteries (pas) in rats. |
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