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...

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Detalles Bibliográficos
Publicado en:Front Neurol
Autores principales: Vilas-Boas, Maria do Carmo, Rocha, Ana Patrícia, Cardoso, Márcio Neves, Fernandes, José Maria, Coelho, Teresa, Cunha, João Paulo Silva
Formato: Artigo
Lenguaje:Inglês
Publicado: Frontiers Media S.A. 2020
Materias:
Neurology
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC7719818/
https://ncbi.nlm.nih.gov/pubmed/33329366
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2020.605282
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