TY  - JOUR
AU  - Dispenzieri, Angela
AU  - Coelho, Teresa
AU  - Conceição, Isabel
AU  - Waddington-Cruz, Márcia
AU  - Wixner, Jonas
AU  - Kristen, Arnt V
AU  - Rapezzi, Claudio
AU  - Planté-Bordeneuve, Violaine
AU  - Gonzalez-Moreno, Juan
AU  - Maurer, Mathew S
AU  - Grogan, Martha
AU  - Chapman, Doug
AU  - Amass, Leslie
AU  - THAOS investigators
PY  - 2022
DO  - 10.1186/s13023-022-02359-w
UR  - http://hdl.handle.net/10668/20339
T2  - Orphanet journal of rare diseases
AB  - Transthyretin amyloidosis (ATTR amyloidosis) is a rare, life-threatening disease caused by the accumulation of variant or wild-type (ATTRwt amyloidosis) transthyretin amyloid fibrils in the heart, peripheral nerves, and other tissues and organs....
LA  - en
KW  - Amyloidosis
KW  - Cardiomyopathy
KW  - Polyneuropathy
KW  - Registry
KW  - Transthyretin
KW  - Amyloid Neuropathies, Familial
KW  - Female
KW  - Genetic Profile
KW  - Humans
KW  - Male
KW  - Phenotype
KW  - Prealbumin
KW  - Surveys and Questionnaires
TI  - Clinical and genetic profile of patients enrolled in the Transthyretin Amyloidosis Outcomes Survey (THAOS): 14-year update.
TY  - research article
VL  - 17
ER  -