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AbstractTransthyretin amyloid cardiomyopathy (ATTR-CM) is an infiltrative cardiomyopathy that results from myocardial deposition of misfolded transthyretin (TTR)…

BackgroundThe diversity of disease phenotypes associated with transthyretin (ATTR) amyloidosis poses challenges for measurement of health outcomes. The…

AbstractObjectiveOur study aimed to report the clinical features and epidemiological characteristics of hereditary transthyretin amyloidosis-polyneuropathy(ATTRv-PN…

AbstractTransthyretin (TTR) amyloidosis is a progressive and fatal disease caused by the deposition of TTR amyloid fibrils in multiple organs and tissues. The…

INTRODUCTIONTransthyretin amyloid cardiomyopathy (ATTR-CM) is a chronic disease caused by transthyretin (TTR) tetramer destabilization and subsequent TTR amyloid…

AbstractObjectives: Proteinuria, amyloidosis, and kidney failure are the main long-term renal complications of familial Mediterranean fever (FMF). This study…

AbstractEnzyme catalysis is essential for molecular transformations. Here, we make use of amyloid, a fibrillar aggregate formed by stacking peptides with β-sheet,…

AbstractBackgroundGrowth-associated protein 43 (GAP-43) is a key protein involved in neuronal growth and synaptic plasticity. Alterations in GAP-43 levels have been…

AbstractAmyloid light-chain (AL) amyloidosis is characterized by the deposition of amyloid fibrils in various organs, although gallbladder involvement is rare. We…

AbstractClinical ConditionCardiac Amyloidosis (CA).Key QuestionsWhen should infiltrative cardiomyopathy be suspected, and what is the differential diagnosis? What…