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Journal Article
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
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 | Amyloidogenesis | Myocardial infarction | Brain | Senile | Heart attacks | Demography | Peptides | Syngeneic grafts | Cardiomyopathy | Laboratories | Liver | Transplantation | Ethics | Body mass index | Calcium-binding protein | Population | Bioindicators | Cardiology | Heart diseases | Genotypes | Public health | Age | Medical personnel | Heart failure | Brain natriuretic peptide | New York | Review boards | Fibrils | Data processing | Renal system | Breast cancer | Coronary heart disease | Mutants | Troponin | Medical prognosis | Light chains | Natriuretic peptide | Data collection | Biomarkers | β-Amyloid | Amyloidosis | Skin | Ventricle | Mutation | Liver transplantation | Kidney transplantation | Cancer | 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 | Research | Biological markers | Health aspects | Risk factors | Natriuretic peptides | Index Medicus | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
Journal Article
Circulation, ISSN 0009-7322, 06/2016, Volume 133, Issue 24, pp. 2404 - +
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 07/2016, Volume 68, Issue 2, pp. 161 - 172
Background Transthyretin amyloidosis (ATTR) is a heterogeneous disorder with multiorgan involvement and a genetic or nongenetic basis. Objectives The goal of... 
transthyretin | amyloid | aging | DIAGNOSIS | POLYNEUROPATHY | CARDIAC & CARDIOVASCULAR SYSTEMS | ACID SCINTIGRAPHY | HEART-FAILURE | PRESERVED EJECTION FRACTION | PREDICTIVE-VALUE | BLACK-AMERICANS | TC-99M-DPD SCINTIGRAPHY | SYSTEMIC AMYLOIDOSIS | MYOCARDIAL-CONTRACTION FRACTION | Peptides | Transplants & implants | Pulmonary arteries | United States--US | Diabetic neuropathy | Family medical history | Multivariate analysis | Quality of life | Confidence intervals | Body mass index | Genotype & phenotype | Mutation | Heart | Demography | ROW other regions of the world | Val122Ile valine-to-isoleucine substitution at position 122 | wt-ATTR wild-type transthyretin amyloidosis | mBMI modified body mass index | TTR-CM transthyretin cardiomyopathy | LVEDD left ventricular end-diastolic dimension | Pain | ATTR transthyretin amyloidosis | Blood pressure | Amyloid | QOL quality of life | Age | Genotypes | BMI body mass index | MCF myocardial contraction fraction | SV stroke volume | Mortality | EDV end-diastolic volume | Data processing | LV left ventricular | Survival | Walking | HFpEF heart failure in the setting of a preserved ejection fraction | TTR transthyretin | mt-ATTR mutated or hereditary transthyretin amyloidosis | Amyloidosis | Amyloid - genetics | Prealbumin - genetics | United States - epidemiology | Prognosis | Survival Rate - trends | Amyloid Neuropathies, Familial - genetics | Amyloid Neuropathies, Familial - metabolism | Humans | Middle Aged | Genotype | Male | Amyloid Neuropathies, Familial - epidemiology | Incidence | Cardiomyopathies - genetics | Cardiomyopathies - epidemiology | Phenotype | Amyloid - metabolism | Prealbumin - metabolism | Cardiomyopathies - metabolism | Female | Registries | Surveys and Questionnaires | Aged | Index Medicus | Abridged Index Medicus | Clinical Medicine | Neurology | Neurologi | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin
Journal Article
Transplantation, ISSN 0041-1337, 09/2015, Volume 99, Issue 9, pp. 1847 - 1854
Background. Until recently, liver transplantation (Ltx) was the only available treatment for hereditary transthyretin (TTR) amyloidosis; today, however,... 
SURVIVAL | SURGERY | POLYNEUROPATHY | FIBRIL COMPOSITION | PROGNOSTIC-FACTORS | CARDIOMYOPATHY | FOLLOW-UP | IMMUNOLOGY | RECIPIENTS | TRANSPLANTATION | PORTUGUESE-TYPE | SWEDISH PATIENTS | PROGRESSION | Liver diseases | Mortality | transthyretin | Heart transplantation | Data processing | survival factor | Multivariate analysis | Polyneuropathy | Survival | Body mass index | Databases | Amyloidosis | Mutation | Age | Kidney transplantation | Liver transplantation | Multivariate Analysis | Prealbumin - genetics | Liver Transplantation - adverse effects | Humans | Middle Aged | End Stage Liver Disease - genetics | Male | Cause of Death | Cardiomyopathies - genetics | End Stage Liver Disease - surgery | Time Factors | Cardiomyopathies - mortality | Adult | Female | Registries | Retrospective Studies | Odds Ratio | Genetic Predisposition to Disease | Time-to-Treatment | Amyloid Neuropathies, Familial - genetics | Risk Factors | Kaplan-Meier Estimate | Proportional Hazards Models | Liver Transplantation - mortality | Logistic Models | Treatment Outcome | Phenotype | End Stage Liver Disease - mortality | Amyloid Neuropathies, Familial - surgery | Age of Onset | Amyloid Neuropathies, Familial - mortality | End Stage Liver Disease - diagnosis | Amyloid Neuropathies, Familial - diagnosis | Index Medicus | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Gastroenterology and Hepatology | Gastroenterologi
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 08/2013, Volume 369, Issue 9, pp. 819 - 829
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 07/2018, Volume 379, Issue 1, pp. 11 - 21
Journal Article