Clinical 3-D Gait Assessment of Patients With Polyneuropathy Associated With Hereditary Transthyretin Amyloidosis
Hereditary amyloidosis associated with transthyretin V30M (ATTRv V30M) is a rare and inherited multisystemic disease, with a variable presentation and a challenging diagnosis, follow-up and treatment. This condition entails a definitive and progressive motor impairment that compromises walking abili...
Main Authors: | Maria do Carmo Vilas-Boas, Ana Patrícia Rocha, Márcio Neves Cardoso, José Maria Fernandes, Teresa Coelho, João Paulo Silva Cunha |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2020-11-01
|
Series: | Frontiers in Neurology |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fneur.2020.605282/full |
Similar Items
-
Corrigendum: Clinical 3-D gait assessment of patients with polyneuropathy associated with hereditary transthyretin amyloidosis
by: Maria do Carmo Vilas-Boas, et al.
Published: (2022-08-01) -
Gait Characterization and Analysis of Hereditary Amyloidosis Associated with Transthyretin Patients: A Case Series
by: Maria do Carmo Vilas-Boas, et al.
Published: (2022-07-01) -
Impact of Vutrisiran on Quality of Life and Physical Function in Patients with Hereditary Transthyretin-Mediated Amyloidosis with Polyneuropathy
by: Laura Obici, et al.
Published: (2023-07-01) -
Portable RGB-D Camera-Based System for Assessing Gait Impairment Progression in ATTRv Amyloidosis
by: Maria do Carmo Vilas-Boas, et al.
Published: (2022-10-01) -
Hereditary transthyretin amyloidosis: a comprehensive review with a focus on peripheral neuropathy
by: Loris Poli, et al.
Published: (2023-10-01)