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Journal Article
Clinical Neurophysiology, ISSN 1388-2457, 07/2019, Volume 130, Issue 7, pp. e113 - e113
Transthyretin familial amyloid polyneuropathy (TTR-FAP) is a rare hereditary disorder caused by mutations in the TTR gene. Unless treated, its course is very... 
Genetic aspects | Polyneuropathies | Medical genetics | Electric properties | Neurophysiology
Journal Article
Journal Article
psychopraxis. neuropraxis, ISSN 2197-9707, 9/2019, Volume 22, Issue 4, pp. 155 - 159
Die rasche Entwicklung innovativer und zunehmend wirksamer Therapien rückt neuromuskuläre Erkrankungen vom Randbereich in den Fokus des neurologischen... 
Therapy | Kardiomyopathie | Medicine & Public Health | Polyneuropathie | Therapie | Cardiomyopathy | Transthyretin | Psychotherapy | Amyloid | Diagnosis hereditary Elektromyography | Polyneuropathy | Diagnose hereditär Elektroneurographie
Journal Article
Clinical Neurophysiology, ISSN 1388-2457, 2016, Volume 127, Issue 9, pp. e237 - e238
Transthyretin-amyloidosis is a life-threatening disease which presents with polyneuropathy as an early sign. However, its diagnosis is often delayed for years.... 
Neurology | Diagnosis | Polyneuropathies | Analysis | Neurophysiology
Journal Article
Journal of Neuromuscular Diseases, ISSN 2214-3599, 2015, Volume 2, Issue s2, pp. S39 - S48
Familial amyloid polyneuropathy related to transthyretin gene (TTR-FAP) is a life-threatening disease transmitted as an autosomal dominant trait. Val30Met... 
epidemiology | amyloidosis | TTR | FAP | dysautonomia | transthyretin | Italy | cardiomyopathy | Familial amyloid polyneuropathy
Journal Article
Clinical Neurophysiology, ISSN 1388-2457, 09/2017, Volume 128, Issue 9, pp. e193 - e193
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1016/j.clinph.2017.07.053 
TTR-FAP | Transthyretin-related familial amyloid polyneuropathy | Management | Genetic aspects | Diagnosis | Polyneuropathies | RNA
Journal Article
INTERNATIONAL JOURNAL OF CANCER, ISSN 0020-7136, 01/2014, Volume 134, Issue 2, pp. 1539 - 1545
Background and purposeThe aim of this study was to assess the effect of Tafamidis, which slows the progression of early stages of Met30 transthyretin (TTR)... 
TRIAL | Tafamidis | LIVER-TRANSPLANTATION | familial amyloid polyneuropathy | Met30 TTR-FAP | HEREDITARY | ONCOLOGY | NEUROPATHIES | Vyndaqel | PRESENTATIONS
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