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The New England Journal of Medicine, ISSN 0028-4793, 07/2018, Volume 379, Issue 1, pp. 22 - 31
Journal Article
JACC: Cardiovascular Imaging, ISSN 1936-878X, 05/2019, Volume 12, Issue 5, pp. 810 - 819
This study evaluated the prognostic potential of native myocardial T1 in cardiac transthyretin amyloidosis (ATTR) and compared native T1 with extracellular... 
CMR | ECV | amyloidosis | ATTR | CARDIAC & CARDIOVASCULAR SYSTEMS | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2019, Volume 14, Issue 2, pp. e0211983 - e0211983
Background The amyloid fibril in hereditary transthyretin (TTR) Val30Met (pVal50Met) amyloid (ATTR Val30Met) amyloidosis is composed of either a mixture of... 
IMPACT | LIVER-TRANSPLANTATION | DEPOSITS | MULTIDISCIPLINARY SCIENCES | ATTR | Phenotype | Amyloidosis | Research
Journal Article
European Journal of Heart Failure, ISSN 1388-9842, 10/2018, Volume 20, Issue 10, pp. 1417 - 1425
Journal Article
Expert Opinion on Orphan Drugs, ISSN 2167-8707, 09/2017, Volume 5, Issue 9, pp. 691 - 699
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
Journal of the Peripheral Nervous System, ISSN 1085-9489, 06/2018, Volume 23, Issue 2, pp. 134 - 137
To present the genetic heterogeneity of a sample of the Brazilian population with transthyretin (TTR) mutations. This cohort study was descriptive and... 
familial amyloid polyneuropathy | ATTR, transthyretin amyloidosis | Brazilian | POLYNEUROPATHY | NEUROPATHY | FAP | VARIANT | NEUROSCIENCES | CLINICAL NEUROLOGY | ATTR | transthyretin amyloidosis | FAMILY | Gene mutations | Genetic research | Amyloidosis | Mutation | Polyneuropathy | Peripheral neuropathy | Population genetics | Transthyretin
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 07/2017, Volume 70, Issue 4, pp. 466 - 477
Journal Article
Annals of Clinical and Translational Neurology, ISSN 2328-9503, 05/2019, Volume 6, Issue 5, pp. 913 - 922
Objective The clinical and genetic profiles of hereditary transthyretin amyloidosis (ATTR) in Chinese populations remain elusive. We aim to characterize the... 
UNINTENTIONAL WEIGHT-LOSS | DIAGNOSIS | POLYNEUROPATHY | MANAGEMENT | NEUROPATHY | PHENOTYPE | ALLELE FREQUENCY | CARDIAC AMYLOIDOSIS | ASSOCIATION | NEUROSCIENCES | CLINICAL NEUROLOGY | ATTR | Haplotypes | Studies | Genotype & phenotype | Medical imaging | Cardiomyopathy | Biopsy | Mutation | Peripheral neuropathy
Journal Article