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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
JACC: Cardiovascular Imaging, ISSN 1936-878X, 2014, Volume 7, Issue 5, pp. 502 - 510
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 11/2018, Volume 394, pp. 78 - 83
Report on the kind and distribution of somatotopic sensation loss and its utility in assessing severity of sensation loss in study of a large international... 
Hereditary transthyretin amyloidosis | Smart somatotopic quantitative sensory testing | Peripheral neuropathy | Familial amyloid polyneuropathy | Sensation loss | TRIAL | TTR-FAP | NERVE | JAPAN | NEUROSCIENCES | CLINICAL NEUROLOGY | FEATURES | Medicine, Experimental | Medical research | Amyloidosis | Polyneuropathies | Analysis | Index Medicus
Journal Article
American Journal of Ophthalmology, ISSN 0002-9394, 08/2018, Volume 192, pp. 169 - 177
To describe abnormalities in choroidal and retinal vasculature associated with Val30Met familial transthyretin amyloidosis (V30M-FTA) using fluorescein and... 
VITREOUS AMYLOIDOSIS | POLYNEUROPATHY | HEREDITARY | INVOLVEMENT | OPHTHALMOLOGY | NEUROPATHIES | OCULAR MANIFESTATIONS | NONFAMILIAL AMYLOIDOSIS | Glaucoma | Genetic aspects | Amyloidosis | Ophthalmology | Neovascularization | Fluorescein | Hypertension | Walking | Medical imaging | Statistical analysis | Mutation | Age
Journal Article
European Journal of Heart Failure, ISSN 1388-9842, 10/2018, Volume 20, Issue 10, pp. 1417 - 1425
Journal Article
Clinical Neurophysiology, ISSN 1388-2457, 06/2019, Volume 130, Issue 6, pp. 903 - 910
To elucidate Aδ-fiber dysfunction at the trunk in patients with hereditary transthyretin (ATTRm) amyloidosis using intra-epidermal electrical stimulation... 
Hereditary transthyretin amyloidosis | Truncal polyneuropathy | Aδ-fiber | Intra-epidermal electrical stimulation | Transthyretin familial amyloid polyneuropathy | Quantitative sensory testing | POLYNEUROPATHY | DETECTION THRESHOLDS | HUMANS | NEUROSCIENCES | CLINICAL NEUROLOGY | DEGENERATION | PERCEPTION | PAIN | NEUROPATHY | A delta-fiber
Journal Article
REVISTA CLINICA ESPANOLA, ISSN 0014-2565, 04/2019, Volume 219, Issue 3, pp. 141 - 144
Background and objective: There are 2 types of amytoidosis caused by transthyretin deposits: the wild type (wt-ATTR) and the mutant type (m-ATTR), transmitted... 
DIAGNOSIS | MEDICINE, GENERAL & INTERNAL | MANAGEMENT | Cardiomyopathy | Hereditary amytoidosis | Transthyretin | Heterogeneous disease | MUTATION | DISEASE | COMMON | Polyneuropathy | CARDIAC AMYLOIDOSIS
Journal Article
Amyloid, ISSN 1350-6129, 01/2018, Volume 25, Issue 1, pp. 54 - 61
Journal Article
Medical Journal of Wuhan University, ISSN 1671-8852, 11/2017, Volume 38, Issue 6, pp. 1013 - 1015
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 04/2014, Volume 9, Issue 1, pp. 61 - 61
Background: Transthyretin amyloidosis is a systemic disorder caused by amyloid deposits formed by misfolded transthyretin monomers. Two main forms exist:... 
Functional | Secondary | Transthyretin | Cardiomyopathies | Amyloid | Amyloidosis | Gastrointestinal disorders | Hereditary | Amyloid neuropathies | Nutritional status | Quality of life | MEDICINE, RESEARCH & EXPERIMENTAL | FECAL INCONTINENCE | POLYNEUROPATHY | LIVER-TRANSPLANTATION | OCULOLEPTOMENINGEAL AMYLOIDOSIS | CLINICAL-FEATURES | LEPTOMENINGEAL AMYLOIDOSIS | ATTR VAL30MET | FAMILIAL AMYLOIDOSIS | GENETICS & HEREDITY | LATE-ONSET | ENDOCRINE-CELLS | Prealbumin - genetics | Gastrointestinal Diseases - physiopathology | Humans | Amyloid Neuropathies, Familial - complications | Quality of Life | Female | Gastrointestinal Diseases - complications | Male | Nutritional Status | Mutation | Amyloid Neuropathies, Familial - physiopathology | Complications and side effects | Care and treatment | Gene mutations | Gastrointestinal diseases | Cardiac patients | Development and progression | Research | Health aspects | Risk factors | Surveys | Albumin | Medicine, Experimental | Medical research | Pharmaceutical industry | Analysis | Transplants & implants | Review boards | Cardiomyopathy | Mortality | Clinical trials | Diarrhea | Nausea | Proteins | Studies | Confidence intervals | Body mass index | Biopsy | Vomiting | Drug therapy | Constipation | Age | Index Medicus | Medical and Health Sciences | Medicin och hälsovetenskap | Gastroenterologi | Klinisk medicin | Clinical Medicine | Gastroenterology and Hepatology
Journal Article