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Kidney International, ISSN 0085-2538, 09/2019, Volume 96, Issue 3, pp. 628 - 641
Amyloidoses are rare life-threatening diseases caused by protein misfolding of normally soluble proteins. The fatal outcome is predominantly due to renal... 
mouse model | glomerular amyloid deposits | hereditary systemic amyloidosis | STOP-CODON MUTATION | DEPOSITION | P-COMPONENT | ATHEROSCLEROSIS | MECHANISMS | INFLAMMATION | IN-VIVO | UROLOGY & NEPHROLOGY | MICE | APOLIPOPROTEIN-A-II | LIPOPROTEINS | Index Medicus | Life Sciences | Human health and pathology
Journal Article
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, ISSN 1619-7070, 03/2018, Volume 45, Issue 3, pp. 452 - 461
Purpose To investigate the utility of Pittsburgh compound B (PiB) positron emission tomography (PET) imaging for evaluating whole-body amyloid involvement in... 
DIAGNOSIS | Amyloid imaging | SCINTIGRAPHY | CARPAL-TUNNEL-SYNDROME | CARDIAC AMYLOIDOSIS | Pittsburgh compound B PET | DEPOSITS | TC-99M-PYROPHOSPHATE | Hereditary transthyretin amyloidosis | F-18-FLORBETAPIR | Amyloid | Light-chain amyloidosis | AL AMYLOIDOSIS | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Journal Article
Amyloid, ISSN 1350-6129, 2008, Volume 15, Issue 1, pp. 40 - 48
Journal Article
Central European Journal of Immunology, ISSN 1426-3912, 2014, Volume 39, Issue 1, pp. 61 - 66
Primary amyloidosis (AL) is a rare variety of plasma cell dyscrasia, the diagnosis of which is often dfficult to establish. Pathogenesis of amyloidosis... 
Immunofixation | AL amyloidosis | Congo red stain | Bone marrow trepanobiopsy | immunofixation | THERAPY | LIGHT-CHAIN AMYLOIDOSIS | HEREDITARY AMYLOIDOSIS | URINE | CLASSIFICATION | bone marrow trepanobiopsy | UPDATE | IMMUNOLOGY | PATHOPHYSIOLOGY | Case Study
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2017, Volume 12, Issue 4, pp. e0173086 - e0173086
Aim: Cardiac troponins and natriuretic peptides are established for risk stratification in light-chain amyloidosis. Data on cardiac biomarkers in transthyretin... 
WILD-TYPE | BRAIN NATRIURETIC PEPTIDE | LIVER-TRANSPLANTATION | FIBRIL COMPOSITION | MYOCARDIAL-INFARCTION | HEREDITARY | MULTIDISCIPLINARY SCIENCES | DISEASE SEVERITY | CARDIOMYOPATHY | TROPONIN-T | SENILE SYSTEMIC AMYLOIDOSIS | Phenotype | Troponin T - blood | Amyloid Neuropathies, Familial - genetics | Humans | Genotype | Surveys and Questionnaires | Biomarkers - blood | Natriuretic Peptide, Brain - blood | Amyloid Neuropathies, Familial - physiopathology | Troponin I - blood | Amyloidosis | Research | Biological markers | Health aspects | Risk factors | Natriuretic peptides | Amyloidogenesis | Myocardial infarction | Brain | Senile | Heart attacks | Demography | Peptides | Syngeneic grafts | Cardiomyopathy | Laboratories | Liver | Transplantation | Ethics | Calcium-binding protein | Population | Bioindicators | Cardiology | Heart diseases | Genotypes | Public health | Age | Medical personnel | Brain natriuretic peptide | Review boards | Fibrils | Data processing | Breast cancer | Coronary artery disease | Mutants | Medical prognosis | Light chains | Data collection | Biomarkers | β-Amyloid | Skin | Ventricle | Mutation | Liver transplantation | Kidney transplantation | Cancer | Index Medicus | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
Journal Article
Journal Article
Российский кардиологический журнал, ISSN 1560-4071, 07/2019, Issue 6, pp. 136 - 142
This article presents a clinical case of a patient with hereditary systemic hereditary transthyretin amyloidosis. Difficulties of diagnostics and differential... 
heart failure | systemic amyloidosis | hereditary amyloidosis | transthyretin amyloidosis
Journal Article
Journal Article
Blood, ISSN 0006-4971, 10/2012, Volume 120, Issue 16, pp. 3206 - 3213
Journal Article