Embodiment Comfort Levels During Motor Imagery Training Combined With Immersive Virtual Reality in a Spinal Cord Injury Patient

Autor: Carla Pais-Vieira, Pedro Gaspar, Demétrio Matos, Leonor Palminha Alves, Bárbara Moreira da Cruz, Maria João Azevedo, Miguel Gago, Tânia Poleri, André Perrotta, Miguel Pais-Vieira

Publikováno v: Frontiers in Human Neuroscience, Vol 16 (2022)

Brain–machine interfaces combining visual, auditory, and tactile feedback have been previously used to generate embodiment experiences during spinal cord injury (SCI) rehabilitation. It is not known if adding temperature to these modalities can res

Externí odkaz: https://doaj.org/article/7f5066b3c5254c34ac00a236e6014eb6

Automatic Resting Tremor Assessment in Parkinson’s Disease Using Smartwatches and Multitask Convolutional Neural Networks

Autor: Luis Sigcha, Ignacio Pavón, Nélson Costa, Susana Costa, Miguel Gago, Pedro Arezes, Juan Manuel López, Guillermo De Arcas

Publikováno v: Sensors, Vol 21, Iss 1, p 291 (2021)

Resting tremor in Parkinson’s disease (PD) is one of the most distinctive motor symptoms. Appropriate symptom monitoring can help to improve management and medical treatments and improve the patients’ quality of life. Currently, tremor is evaluat

Externí odkaz: https://doaj.org/article/802ef8c871d849e896aa14cf119cdaaf

Multimodal Visual, Auditory, Thermal, and Tactile Feedback During Brain-Machine Interface Use by a Spinal Cord Injury Patient

Autor: Carla Paisv, Pedro Gaspar, Tânia Poleri, Demétrio Matos, Maria Azevedo, Miguel Gago, André Perrotta, Miguel Vieira

Background: Brain-machine interfaces (BMIs) have the potential to replace and expand body functions, but also to induce neuroplasticity. In BMIs that include virtual reality and tactile feedback, it is thought that the underlying mechanism may be par

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24ce23fcc54d89d7e45c5773a245e5a3
http://doi.org/10.54941/ahfe100912

Founder effect of Fabry disease due to p.F113L mutation: Clinical profile of a late-onset phenotype

Autor: Emilia Lopes, Rui Faria, Paulo Gaspar, Olga Azevedo, Alice Martins, Jorge Rodrigues, Sónia Simões, Gabriel Miltenberger-Miltenyi, Pedro Reimão, Nuno Sousa, Olga Pereira, Damião Cunha, Fátima Dias, Miguel Gago, Andreas Gal, Maria José Guimarães

Publikováno v: Molecular Genetics and Metabolism. 129:150-160

Background Knowledge on clinical profiles of late-onset phenotypes of Fabry disease (FD) is essential to better define their natural history. Our study aims to demonstrate a founder effect of FD due to the GLA gene mutation c.337T>C (p.F113L) in the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df03cb27173cb895c2f6d02ec72b6977
https://doi.org/10.1016/j.ymgme.2019.07.012

Fabry Disease Therapy: State-of-the-Art and Current Challenges

Autor: Damião Cunha, Nuno Sousa, Miguel Gago, Gabriel Miltenberger-Miltenyi, Olga Azevedo

Publikováno v: International Journal of Molecular Sciences, Vol 22, Iss 206, p 206 (2021)
International Journal of Molecular Sciences
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP

Fabry disease (FD) is a lysosomal storage disorder caused by mutations of the GLA gene that lead to a deficiency of the enzymatic activity of α-galactosidase A. Available therapies for FD include enzyme replacement therapy (ERT) (agalsidase alfa and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d0c527100f41e27f1e07a545ed3f939
https://www.mdpi.com/1422-0067/22/1/206