专题:Vascular Anomalies and Treatments

This cluster of papers focuses on the diagnosis and management of hereditary hemorrhagic telangiectasia (HHT), a genetic disorder characterized by vascular malformations. It covers topics such as genetics, pulmonary arteriovenous malformations, embolization, epistaxis, liver involvement, SMAD4 mutations, and vascular anomalies.
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Transforming Pulmonary Arterial Hypertension: Key Milestones and Future Perspectives

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Haemodynamic responses to sotatercept and parenteral prostacyclins in pulmonary arterial hypertension patients

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Activin A–Endothelin-1 Axis Governs Pulmonary Vascular Remodeling: Mechanistic Basis for Emerging Therapies in PAH

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Long-term effects of medical therapy pre- and post-pulmonary endarterectomy—insights from the UK CURATE registry

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Clinical spectrum of hereditary hemorrhagic telangiectasia: data from the Comprehensive HHT Outcomes Registry of the US (CHORUS)

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Sotatercept in Pulmonary Arterial Hypertension

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Characteristics associated with clinical response to pomalidomide in hereditary hemorrhagic telangiectasia

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Pathophysiology and prevalence of high output heart failure in group 1 pulmonary hypertension

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The International/Canadian hereditary angioedema guideline

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Breast Cancer Reveals Latent BMPR2 -Related Susceptibility to Pulmonary Hypertension

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