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If you’ve been diagnosed with the rare diseases of multiple myeloma or amyloidosis, it’s important to be evaluated by hematology experts before beginning treatment…

AbstractWe report the case of an 82-year-old male with a history of bronchiectasis, asthma, and atrial fibrillation, who presented with progressive exertional…

AbstractINTRODUCTIONWe investigated whether older adults with subjective memory complaints (SMC) and amyloid‐β accumulation may show clinical progression over 2…

AbstractAims: The role of sodium-glucose co-transporter 2 inhibitors (SGLT2i) in patients with cardiac amyloidosis (CA) is controversial. However, they have shown…

AbstractBackground: Amyloidosis is the extracellular accumulation of amyloid proteins in diverse organs. While ocular and periocular involvement is rare, it can be…

AbstractAmyloid light-chain (AL) amyloidosis, which results from monoclonal light-chain deposition from plasma cell dyscrasia, is often identified in old patients.…

AbstractBackground and AimsConcomitant aortic stenosis (AS) and transthyretin-associated cardiac amyloidosis (ATTR-CA) is an increasingly recognized cause of…

AbstractThe appearance of new treatments for the different forms of ATTR has highlighted the importance of early diagnosis, since most of these treatments are…

Background/Objectives: Cardiac amyloidosis (CA) is an underdiagnosed and potentially life-threatening infiltrative cardiomyopathy characterized by the extracellular…

AbstractOver 150 transthyretin (TTR) mutations have been identified in hereditary transthyretin (ATTRv) amyloidosis, and new TTR variants have recently emerged.…