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Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2013, Volume 8, Issue 1, pp. 31 - 31
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 07/2016, Volume 68, Issue 2, pp. 161 - 172
Journal Article
Clinical Autonomic Research, ISSN 0959-9851, 9/2019, Volume 29, Issue S1, pp. 19 - 24
Autonomic dysfunction is a very common, early and distressing aspect of hereditary transthyretin (ATTR) amyloidosis leading to significant loss of quality of... 
Transthyretin | Dysautonomia | Neuropathy | Neurology | Autonomic dysfunction | Tafamidis | Medicine & Public Health | Gastroenterology | Amyloidosis | Diabetes | Ophthalmology | Cardiology | Endocrinology | Orthostatic hypotension | Literature reviews | Phenotypes | Autonomic nervous system | Clinical trials | Peripheral neuropathy | Patients | Morbidity | Quality of life | Review
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 07/2018, Volume 379, Issue 1, pp. 22 - 31
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 08/2016, Volume 375, Issue 6, pp. 511 - 522
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 12/2015, Volume 10, Issue 1, p. 109
Journal Article
Muscle & Nerve, ISSN 0148-639X, 11/2017, Volume 56, Issue 5, pp. 901 - 911
Polyneuropathy signs (Neuropathy Impairment Score, NIS), neurophysiologic tests (m+7.sub.Ionis), disability, and health scores were assessed in baseline... 
disability | familial amyloidotic polyneuropathy (FAP) | oligonucleotide trials | polyneuropathy signs | peripheral neuropathy | neurophysiologic tests | proficiency | Medicine, Experimental | Medical research | Nervous system diseases | Genetic aspects | Polyneuropathies | Neurophysiology | Evaluation | Pain perception | Pain | Health | Neuropathy | Polyneuropathy
Journal Article
Muscle & Nerve, ISSN 0148-639X, 05/2018, Volume 57, Issue 5, pp. 829 - 837
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
Arquivos de Neuro-Psiquiatria, ISSN 0004-282X, 09/2018, Volume 76, Issue 9, pp. 609 - 621
Transthyretin familial amyloid polyneuropathy is an autosomal dominant inherited sensorimotor and autonomic polyneuropathy, which if untreated, leads to death... 
Allografts | Syngeneic grafts | Autonomic nervous system | Transthyretin | Sensorimotor system | Amyloid | Diagnosis | Polyneuropathy | Peripheral neuropathy | Liver transplantation | polyneuropathies | amyloid neuropathies, familial
Journal Article