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European Heart Journal|October 14, 2022
Cardiovascular magnetic resonance in light-chain amyloidosis to guide treatmentAna Martinez-Naharro, Rishi Patel, Tushar Kotecha, et al.
Circulation|May 22, 2019
Natural History, Quality of Life, and Outcome in Cardiac Transthyretin AmyloidosisThirusha Lane, Marianna Fontana, Ana Martinez-Naharro, et al.
Circulation. Cardiovascular Imaging|April 20, 2021
Cardiac Magnetic Resonance-Derived Extracellular Volume Mapping for the Quantification of Hepatic and Splenic AmyloidLiza Chacko, Michele Boldrini, Raffaele Martone, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|December 7, 2025
New Validated Staging System for Light Chain (AL) Amyloidosis With Stage IIIC Defining Ultra-Poor Risk: AL International Staging SystemJahanzaib Khwaja, Amy A Kirkwood, Paolo Milani, et al.
JAMA Cardiology|August 21, 2024
Redefining Cardiac Involvement and Targets of Treatment in Systemic Immunoglobulin AL AmyloidosisAldostefano Porcari, Ambra Masi, Ana Martinez-Naharro, et al.
European Journal of Heart Failure|November 13, 2023
Deep phenotyping of p.(V142I)-associated variant transthyretin amyloid cardiomyopathy: Distinct from wild-type transthyretin amyloidosis?Yousuf Razvi, Adam Ioannou, Rishi K Patel, et al.
European Heart Journal|March 22, 2023
Tc-99m labelled bone scintigraphy in suspected cardiac amyloidosisMuhammad Umaid Rauf, Philip N Hawkins, Francesco Cappelli, et al.
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