Last Updated: 09/26/2026
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Found 17 publications
Large Language Model Summarization of Physician-to-Physician Calls for Interhospital Transfer of Patients With ST-Elevation Myocardial Infarction: Observational Study.
Journal: Journal of medical Internet research
Published: December 02, 2025
The Therapeutic Impact of Genetic Evaluation in an Atrial Fibrillation Precision Medicine Clinic.
Journal: medRxiv : the preprint server for health sciences
Published: April 08, 2025
Genetic evaluation of early-onset atrial fibrillation: impact on patient management.
Journal: European heart journal
Published: March 31, 2025
Clinical Characteristics and Outcomes in Patients With Atrial Fibrillation and Pathogenic TTN Variants.
Journal: JACC. Clinical electrophysiology
Published: May 23, 2024
Hereditary hemorrhagic telangiectasia may be the most morbid inherited bleeding disorder in women.
Journal: Blood advances
Published: October 23, 2023
Avatrombopag for adults with early versus chronic immune thrombocytopenia.
Journal: American journal of hematology
Published: July 23, 2023
Antithrombotic therapy for atrial fibrillation in hereditary hemorrhagic telangiectasia.
Journal: Journal of thrombosis and thrombolysis
Published: May 27, 2023
Cardiac Sarcoidosis and a Likely Pathogenic TTN Variant in a Patient Presenting With Ventricular Tachycardia.
Journal: JACC. Case reports
Published: February 05, 2023
Anticoagulation and antiplatelet therapy in hereditary hemorrhagic telangiectasia: A scoping review.
Anticoagulation and antiplatelet therapy in hereditary hemorrhagic telangiectasia: A scoping review.
Journal: Thrombosis research
Published: January 30, 2023
Patient Selection, Techniques, and Complication Mitigation for Epicardial Ventricular Tachycardia Ablation.
Journal: Cardiac electrophysiology clinics
Published: November 17, 2022
Safety, tolerability, and effectiveness of anticoagulation and antiplatelet therapy in hereditary hemorrhagic telangiectasia.
Journal: Journal of thrombosis and haemostasis : JTH
Published: July 19, 2022
Systemic bevacizumab as salvage therapy for persistent severe bleeding and anemia in heyde syndrome following aortic valve replacement.
Journal: Journal of thrombosis and thrombolysis
Published: June 19, 2022
Last Updated: 09/26/2026