Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Anabela Farias"'
Publikováno v:
Acta Médica Portuguesa, Vol 20, Iss 5 (2008)
Neurofibromatosis type 1 (NF1) is one of the most common neurocutaneous disorders. It is an autosomal dominant hereditary condition, although an half of all cases are related with spontaneous mutations. Mutations within NF1 gene (c17q11.2) result in
Externí odkaz:
https://doaj.org/article/55281e26220244039742e30bdce50271
Autor:
Rodrigo Ventura, Daniel Faustino de Noronha Osório, Jhielson M. Pimentel, Luís Luz, Francisco S. Melo, Plinio Moreno, Miguel Faria, Mithun Kinarullathil, David Belo, Pedro U. Lima, Alberto Sardinha, Pedro Sequeira, Miguel Vasco, Rubén Solera-Ureña, Anabela Farias, Marta Couto, Hugo Gamboa, Andre Mateus, Cátia Jesus, Ana Paiva, João Rodrigues, Manuela Veloso, Isabel Melo
Publikováno v:
Artificial intelligence in medicine. 96
This paper describes the INSIDE system, a networked robot system designed to allow the use of mobile robots as active players in the therapy of children with autism spectrum disorders (ASD). While a significant volume of work has explored the impact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf44b61d26c1dd8e821400cb2ae01116
https://pubmed.ncbi.nlm.nih.gov/30598330
https://pubmed.ncbi.nlm.nih.gov/30598330
Autor:
Cristina L, Martins, J Paulo, Monteiro, Anabela, Farias, Rita, Fernandes, Maria José, Fonseca
Publikováno v:
Acta medica portuguesa. 20(5)
Neurofibromatosis type 1 (NF1) is one of the most common neurocutaneous disorders. It is an autosomal dominant hereditary condition, although an half of all cases are related with spontaneous mutations. Mutations within NF1 gene (c17q11.2) result in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e3a37a7f5bca02d93342243e5db6b9f7
https://pubmed.ncbi.nlm.nih.gov/18282435
https://pubmed.ncbi.nlm.nih.gov/18282435