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Medicine (Spain), ISSN 0304-5412, 05/2013, Volume 11, Issue 34, pp. 2065 - 2075
Amyloidosis are a heterogeneous group of diseases in which proteins, usually soluble in plasma, are deposited in the extracellular space and insoluble... 
AL amyloidosis | AA amyloidosis | Amyloid | Amyloidosis | Familial amyloidotic polyneuropathy
Journal Article
Journal Article
Clinical Medicine, Journal of the Royal College of Physicians of London, ISSN 1470-2118, 04/2018, Volume 18, Issue 2, pp. s30 - s35
Systemic amyloidosis comprises an uncommon group of disorders caused by the extracellular deposition of misfolded proteins in various organs. Cardiac amyloid... 
AL amyloidosis | CMR | Cardiac amyloidosis | Infiltrative cardiomyopathy | ATTR amyloidosis | infiltrative cardiomyopathy | ANTIBODIES | DIAGNOSIS | MEDICINE, GENERAL & INTERNAL | LIGHT-CHAIN AMYLOIDOSIS | CYCLOPHOSPHAMIDE | CARDIOVASCULAR MAGNETIC-RESONANCE | cardiac amyloidosis | BORTEZOMIB
Journal Article
Clinical medicine (London, England), ISSN 1470-2118, 04/2018, Volume 18, Issue Suppl 2, pp. s30 - s35
Systemic amyloidosis comprises an uncommon group of disorders caused by the extracellular deposition of misfolded proteins in various organs. Cardiac amyloid... 
infiltrative cardiomyopathy | cardiac amyloidosis | AL amyloidosis | CMR | Cardiology | ATTR amyloidosis
Journal Article
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 07/2017, Volume 70, Issue 4, pp. 466 - 477
Journal Article
Circulation Journal, ISSN 1346-9843, 2019, Volume 83, Issue 4, pp. 775 - 782
Background: Cardiac involvement occurs in more than half of the patients with light-chain amyloidosis (AL), but the characteristics, treatment and prognosis of... 
Bortezomib | NT-proBNP | Cardiac amyloidosis | Light-chain amyloidosis | SURVIVAL | DEXAMETHASONE | CARDIAC & CARDIOVASCULAR SYSTEMS | EFFICACY | CYCLOPHOSPHAMIDE | PRIMARY SYSTEMIC AMYLOIDOSIS | FEATURES | STAGING SYSTEM | BIOMARKERS | AL AMYLOIDOSIS
Journal Article
Medicine, ISSN 1357-3039, 2017, Volume 45, Issue 5, pp. 318 - 321
Abstract Amyloidosis is a rare group of disorders with protean manifestations characterized by tissue deposition of misfolded protein. Removal of such deposits... 
Internal Medicine | SAP scan | AL amyloid | amyloidosis | chemotherapy | stem cell transplantation
Journal Article
Journal Article
Circulation, ISSN 0009-7322, 01/2005, Volume 111, Issue 2, pp. 186 - 193
Journal Article