Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Diana Maria Cubillos-Arcila"'
Autor:
Samanta Ferraresi Brighente, Paul Vicuña, Ana Luiza Rodrigues Louzada, Gabriela Marchisio Giordani, Helena Fussiger, Marco Antonnio Rocha Dos Santos, Diana Maria Cubillos-Arcila, Pablo Brea Winckler, Jonas Alex Morales Saute
Publikováno v:
PLoS ONE, Vol 16, Iss 11, p e0259397 (2021)
IntroductionThe Hereditary Spastic Paraplegias (HSP) are a group of genetic diseases that lead to slow deterioration of locomotion. Clinical scales seem to have low sensitivity in detecting disease progression, making the search for additional biomar
Externí odkaz:
https://doaj.org/article/6ce0e04d383f43f6895e06e73da0bc83
Autor:
Diana Maria Cubillos Arcila, Gustavo Dariva Machado, Valéria Feijó Martins, Vanessa Bielefeldt Leotti, Rebecca Schüle, Leonardo Alexandre Peyré-Tartaruga, Jonas Alex Morales Saute
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
IntroductionHereditary spastic paraplegias (HSPs) are a heterogeneous group of neurodegenerative diseases in which little is known about the most appropriate clinical outcome assessments (COAs) to capture disease progression. The objective of this st
Externí odkaz:
https://doaj.org/article/88f24352aa8f4075b514d283f6704bbe
Autor:
Diana Maria Cubillos-Arcila, Valéria Feijó Martins, Ana Paula Janner Zanardi, Gustavo Dariva Machado, Daniela Burguêz, Natalia Andrea Gomeñuka, Leonardo Alexandre Peyré-Tartaruga, Jonas Alex Morales Saute
Background: Motor and somatosensory pathways dysfunction due to degeneration of long tracts in hereditary spastic paraplegias (HSP) indicates that postural abnormalities may be a relevant disease feature. However, balance assessments have been underu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b711a01c68c12cf5adae6734d5caa431
https://doi.org/10.21203/rs.3.rs-2036550/v1
https://doi.org/10.21203/rs.3.rs-2036550/v1
Autor:
Diana Maria Cubillos-Arcila, Jonas Alex Morales Saute, Paul Vicuña, Helena Fussiger, Samanta Ferraresi Brighente, Pablo Brea Winckler, Gabriela Marchisio Giordani, Ana Luiza Rodrigues Louzada, Marco Antonnio Rocha dos Santos
Publikováno v:
PLoS ONE
PLoS ONE, Vol 16, Iss 11, p e0259397 (2021)
PLoS ONE, Vol 16, Iss 11, p e0259397 (2021)
Introduction The Hereditary Spastic Paraplegias (HSP) are a group of genetic diseases that lead to slow deterioration of locomotion. Clinical scales seem to have low sensitivity in detecting disease progression, making the search for additional bioma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f2f78ee9b89e85c629ef088b55227c3
http://europepmc.org/articles/PMC8631666
http://europepmc.org/articles/PMC8631666
Autor:
Daniela Burguêz, Lauren Sehnem, Gustavo Dariva Machado, Leonardo Alexandre Peyré-Tartaruga, Valéria Feijó Martins, Jonas Alex Morales Saute, Ana Paula Janner Zanardi, Diana Maria Cubillos-Arcila
Publikováno v:
Cerebellum (London, England). 21(3)
Hereditary spastic paraplegias (HSP) are characterized by progressive deterioration of axonal projections of upper motor neurons leading to abnormal locomotion. The clinical course of HSP as well as the definition of the best instruments to assess it
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a56dd6d1c766d00f340bfeebd424356
https://pubmed.ncbi.nlm.nih.gov/34244902
https://pubmed.ncbi.nlm.nih.gov/34244902