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Annals of the Rheumatic Diseases, ISSN 0003-4967, 04/2016, Volume 75, Issue 4, pp. 644 - 651
Journal Article
European heart journal, ISSN 0195-668X, 06/2019, Volume 40, Issue 21, pp. 1661 - 1664
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2015, Volume 10, Issue Suppl 1, p. I10
Journal Article
NEW ENGLAND JOURNAL OF MEDICINE, ISSN 0028-4793, 11/2018, Volume 379, Issue 21, pp. 2086 - 2086
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 10/2018, Volume 72, Issue 15, p. 1881
Journal Article
New England Journal of Medicine, ISSN 0028-4793, 04/2015, Volume 372, Issue 18, p. 1769
Journal Article
British Journal of Haematology, ISSN 0007-1048, 08/2019, Volume 186, Issue 3, pp. 460 - 470
Systemic AL amyloidosis is a cause of type 5 cardiorenal syndrome. Response to treatment is currently reported according to organ‐specific amyloidosis... 
NT‐proBNP | dialysis | Amyloidosis | Cardiorenal | Cardiology | Natriuretic peptides | Heart | Renal function | Kidneys | Epidermal growth factor receptors | Hemodialysis | Mortality | Glomerular filtration rate | Biomarkers | Death | Dialysis | Bioindicators | Diagnosis | Stratification | Proteinuria
Journal Article
Heart, ISSN 1355-6037, 03/2019, Volume 105, Issue Suppl 3, p. A18
BackgroundCardiac amyloidosis (CA) has been associated with a high prevalence of intracardiac thrombi, but this was reported in small cohorts of high risk... 
Blood clots
Journal Article
Arthritis & Rheumatology, ISSN 2326-5191, 08/2016, Volume 68, Issue 8, pp. 2044 - 2049
To investigate the molecular cause of persistent fevers in a patient returning from working overseas, in whom investigations for tropical diseases yielded... 
Sequence Deletion | Humans | Fever - genetics | Adult | Male | Mosaicism | Receptors, Tumor Necrosis Factor, Type I - genetics | Hereditary Autoinflammatory Diseases - genetics | Gangrene | Tumor necrosis factor-TNF | Sperm | Rodents | Index Medicus | Abridged Index Medicus
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 10/2018, Volume 72, Issue 15, pp. 1881 - 1881
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
Arthritis and Rheumatology, ISSN 2326-5191, 2014, Volume 66, Issue 1, pp. 197 - 202
Objective. To identify the genetic cause of chronic infantile neurologic, cutaneous, articular syndrome (CINCA syndrome) using whole-exome sequencing in a... 
MUCKLE-WELLS-SYNDROME | GENETIC-VARIANTS | MUTATIONS | RHEUMATOLOGY | GALAXY | Brief Report
Journal Article
Rheumatology, ISSN 1462-0324, 04/2016, Volume 55, Issue suppl_1, pp. i83 - i83
Journal Article
PEDIATRIC RHEUMATOLOGY, ISSN 1546-0096, 07/2019, Volume 17, Issue 1, pp. 36 - 36
BackgroundCryopyrin-associated periodic syndrome (CAPS) is a rare autoinflammatory disease, caused by gain of function mutation in NLRP3 resulting in excess... 
Paediatric | Cryopyrin-associated periodic syndrome (CAPS) | PEDIATRICS | RHEUMATOLOGY | Canakinumab | Child | Vial-sharing | Drugs | Evaluation | Drug delivery systems | Cryopyrin-associated periodic syndromes | Economic aspects | Drug therapy | Pediatric research | Vehicles
Journal Article
Blood, ISSN 0006-4971, 11/2014, Volume 124, Issue 19, pp. 3025 - 3027
Journal Article
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