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Neurology, ISSN 0028-3878, 08/2012, Volume 79, Issue 8, pp. 785 - 792
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 07/2016, Volume 68, Issue 2, pp. 161 - 172
Journal Article
Transplantation, ISSN 0041-1337, 09/2015, Volume 99, Issue 9, pp. 1847 - 1854
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 12/2016, Volume 87, Issue 12, pp. e1 - e1
BackgroundFamilial Amyloid Polyneuropathy (FAP) is a progressive disease caused by deposition of transthyretin (TTR). Patisiran is an investigational, small... 
SURGERY | PSYCHIATRY | CLINICAL NEUROLOGY | Neurologi | Basic Medicine | Neurosciences | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin | Kirurgi | Clinical Medicine | Neurology | Surgery | Medicinska och farmaceutiska grundvetenskaper | Psykiatri | Psychiatry | Neurovetenskaper
Journal Article
Arquivos Brasileiros de Cardiologia, ISSN 1678-4170, 09/2015, Volume 105, Issue 5, pp. 503 - 509
Background:Familial amyloidotic polyneuropathy (FAP) is a rare disease diagnosed in Brazil and worldwide. The frequency of cardiovascular involvement in... 
CARDIAC & CARDIOVASCULAR SYSTEMS
Journal Article
BMC NEUROLOGY, ISSN 1471-2377, 06/2019, Volume 19, Issue 1, pp. 146 - 146
BackgroundFamilial amyloid polyneuropathy (FAP) or ATTRv (amyloid TTR variant) amyloidosis is a fatal hereditary disease characterized by the deposition of... 
TARGET | Cytokines | Transthyretin | TRANSTHYRETIN AMYLOIDOSIS | RELEASE | Familial amyloid polyneuropathy | VAL30MET | CLINICAL NEUROLOGY | MOUSE MODEL | Biomarkers | Amyloid | STRESS | EXPRESSION | Development and progression | Genetic aspects | Amyloidosis | Inflammation | Corticosteroids | Polyneuropathies
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 12/2015, Volume 10, Issue 1, pp. 109 - 109
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 09/2018, Volume 379, Issue 11, pp. 1007 - 1016
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 | Coronary heart disease
Journal Article
Arquivos de Neuro-Psiquiatria, ISSN 0004-282X, 02/2019, Volume 77, Issue 2, pp. 96 - 100
Transthyretin amyloidosis (ATTR) is characterized by the deposit of mutant or wild-type transthyretin that forms amyloid fibrils, which are extracellularly... 
Polyneuropathy | Amyloidosis | Amyloid neuropathies, familial | amyloid neuropathies | familial | PSYCHIATRY | NEUROSCIENCES | polyneuropathy | Geographical distribution | Demography | Platelet-activating factor | Fibrils | Transthyretin | Family medical history | Neuropathy | Autonomic nervous system | Sensorimotor system | Amyloid | Mutation | Diagnosis | Age | Genotypes | amyloid neuropathies, familial
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 08/2019, Volume 403, pp. 1 - 6
Despite growing numbers of patients diagnosed with late-onset hereditary ATTR V30M amyloidosis with polyneuropathy (ATTRv-PN), this condition remains poorly... 
Hereditary transthyretin amyloidosis | Early-onset ATTRv-PN | Polyneuropathy | Late-onset ATTRv-PN | Familial amyloid polyneuropathy | Polyneuropathies | Amyloidosis
Journal Article