Phenotypes of idiopathic pulmonary arterial hypertension
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine
Reference4 articles.
1. Phenotyping of idiopathic pulmonary arterial hypertension: a registry analysis;Hoeper;Lancet Respir Med,2022
2. EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension;Eyries;Nat Genet,2014
3. Letter by Hernandez-Gonzalez et al regarding article, “Phenotypic characterization of EIF2AK4 mutation carriers in a large cohort of patients diagnosed clinically with pulmonary arterial hypertension”;Hernandez-Gonzalez;Circulation,2018
4. Radiological findings in Multidetector Computed Tomography (MDCT) of hereditary and sporadic pulmonary veno-occlusive disease: certainties and uncertainties;Pérez Núñez;Diagnostics (Basel),2021
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3. Prognostic Stratification and Treatment for Pulmonary Arterial Hypertension. Gaps and Promising Remedies;Archivos de Bronconeumología;2023-10
4. Canagliflozin alleviates pulmonary hypertension partially by inhibition of PPARγ S225 phosphorylation and PPARγ-mediated suppression of oxidative stress;2023-04-20
5. Novel Molecular Mechanisms Involved in the Medical Treatment of Pulmonary Arterial Hypertension;International Journal of Molecular Sciences;2023-02-19
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