Dynamic left main coronary artery compression by a dilated pulmonary artery in a patient with pulmonary hypertension-a case report demonstrating the significance of multimodular imaging. [PDF]
Lebbink JS +4 more
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Takotsubo cardiomyopathy during armed conflict: A case series
ESC Heart Failure, Volume 12, Issue 2, Page 1494-1498, April 2025.
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Interruption of the right middle and lower lobe pulmonary arteries combined with arterial aneurysm formation at the origin of the right subclavian artery branch: a case report. [PDF]
Hou C, Zhao G.
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Longest survivor of pulmonary atresia with ventricular septal defect without surgical intervention
ESC Heart Failure, Volume 12, Issue 2, Page 1499-1507, April 2025.
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Reduced Circulating HIF-1α, HIF-2α, HIF-3α, and VHL Levels in Patients With Pulmonary Arterial Hypertension. [PDF]
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Erratum: Chinese Herbal Medicine in Hypoxic Pulmonary Hypertension Treatment: Mechanisms, Progress, and Future Directions [Corrigendum]. [PDF]
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Pulmonary hypertension (PH) is a chronic and progressive disease that presents like many other lung diseases, often leading to a delay in diagnosis, and therefore a delay in optimal therapy. This article provides a review of PH for internists, covering clinical presentation, diagnostic algorithm, different types of PH, and overview of treatments.
Darlene, Kim, M Patricia, George
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Pulmonary hypertension can be caused by an increase in pulmonary blood flow, an increase in left-heart impedance or an increase in pulmonary vascular resistance. Although there are many specific causes that have been identified, clinical presentation and natural history are common to all etiologies.
D, Moraes, J, Loscalzo
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