TY  - JOUR
AU  - Conceição, Isabel
AU  - Damy, Thibaud
AU  - Romero, Manuel
AU  - Galán, Lucía
AU  - Attarian, Shahram
AU  - Luigetti, Marco
AU  - Sadeh, Menachem
AU  - Sarafov, Stayko
AU  - Tournev, Ivailo
AU  - Ueda, Mitsuharu
PY  - 2019
DO  - 10.1080/13506129.2018.1556156
UR  - http://hdl.handle.net/10668/13609
T2  - Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
AB  - Diagnosis in the early stages of hereditary transthyretin (ATTR) amyloidosis is imperative to support timely treatment to prevent or delay disease progression. Genetic testing in the setting of genetic counselling enables identification of carriers of...
LA  - en
KW  - ATTR
KW  - amyloidosis
KW  - carrier
KW  - diagnosis
KW  - follow up
KW  - hereditary
KW  - minimum criteria for diagnosis
KW  - predicted age of disease onset
KW  - transthyretin
KW  - Age of Onset
KW  - Amyloid Neuropathies, Familial
KW  - Early Diagnosis
KW  - Genetic Testing
KW  - Humans
KW  - Medical History Taking
KW  - Mutation
KW  - Practice Guidelines as Topic
KW  - Prealbumin
TI  - Early diagnosis of ATTR amyloidosis through targeted follow-up of identified carriers of TTR gene mutations.
TY  - research article
VL  - 26
ER  -