期刊： AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2020; 27 (1)
Background: Amyloid light chain (AL) amyloidosis is characterized by tissue deposition of amyloid fibres derived from immunoglobulin that can lead to ......
期刊： AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2019; 26 (1)
Background: T1 mapping allows quantitative assessment of diffuse deposition of amyloid protein in the myocardium. Early detection of cardiac involveme......
期刊： AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2019; 26 (2)
Background: Patients with amyloid light-chain (AL) amyloidosis who have advanced cardiac damage are at risk of premature mortality. Currently, bortezo......
期刊： AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2019; 26 (4)
Background: Renal involvement is one of the most common complications of light-chain (AL) amyloidosis. For evaluating renal prognosis, two staging sys......
期刊： AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2017; 24 (1)
Hereditary amyloid polyneuropathy is a type of protein misfolding disease. Transthyretin (TTR) is a homotetrameric serum protein and TTR tetramer diss......
