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Amyloid, ISSN 1350-6129, 07/2017, Volume 24, Issue 3, pp. 194 - 204
Background: The objective of the present study was to evaluate the long-term safety and efficacy of tafamidis in treating hereditary transthyretin amyloid... 
ATTRV30M | Amyloidosis | disease-modifying drug | non-ATTRV30M | SURVIVAL | MEDICINE, RESEARCH & EXPERIMENTAL | STABILIZATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | VAL30MET | TRANSPLANTATION | TRIAL | MEDICINE, GENERAL & INTERNAL | FAP | MUTATIONS | OUTCOMES | REGISTRY | Index Medicus
Journal Article
Journal Article
Journal of Genetic Counseling, ISSN 1059-7700, 8/2013, Volume 22, Issue 4, pp. 437 - 447
Genetic counselling must be offered in the context of presymptomatic testing (PST) for severe late-onset diseases; however, effective genetic counselling is... 
Human Genetics | Familial amyloid polyneuropathy type 1 | Public Health | Gynecology | Huntington disease | Clinical Psychology | Neurodegenerative disorders | SCA | Ethics | Biomedicine | Spinocerebellar ataxia | FAP ATTRV30M | Consultand’s perspective | Quality assessment | Genetic testing
Journal Article
Biochemistry and Biophysics Reports, ISSN 2405-5808, 12/2016, Volume 8, pp. 48 - 54
Penetrance and age of onset of ATTRV30M amyloidotic neuropathy varies significantly among different populations. This variability has been attributed to both... 
ATTRV30M | Genetic background | Amyloid
Journal Article
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