ATTR-CM, HFpEF, and Clinical Cardiology: It Is Not a Moment, It Is a Movement. [PDF]
Nayak GS.
europepmc +1 more source
Transthyretin amyloid cardiomyopathy (ATTR-CM) is an infiltrative cardiomyopathy resulting from age-related failure of homoeostatic mechanisms in wild-type ATTR (wtATTR-CM) or destabilizing mutations in variant TTR (vATTR-CM). Atrial fibrillation (AF) is
Melpignano, Angelo +12 more
core +1 more source
Suspecting and diagnosing transthyretin amyloid cardiomyopathy (ATTR-CM) in India: An Indian expert consensus. [PDF]
Chander Mohan J +11 more
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Identifying Suspected ATTR-CM From Unstructured EHR Data Using AI. [PDF]
Batinica B, Cheng RK, Khera R.
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The Promise and Pitfalls of TTR Stabilization Assays in ATTR-CM. [PDF]
Witteles RM.
europepmc +1 more source
ATTR-CM in Patients With Clinically Significant Plasma Cell Dyscrasias: A Case Series Highlighting Diagnostic Challenges. [PDF]
Ancha B +11 more
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Patient Perspectives on Transthyretin Amyloid Cardiomyopathy (ATTR-CM) Treatment Attributes. [PDF]
Kumar N +10 more
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Background Diagnosis of cardiac amyloidosis (CA) is complex and implicates several medical specialists. CA is usually suspected based on symptoms (‘red flags’) and non-invasive imagery.
Charron, Philippe +37 more
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Evaluation of the Current ATTR-CM Treatment Landscape via a Mathematical Model of TTR Dissociation and Amyloid Formation. [PDF]
Methven Jeknić S +6 more
europepmc +1 more source
The First Korean Clinical Evidence With Tafamidis in ATTR-CM. [PDF]
Lee J, Oh J.
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