Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Luis Negrão"'
Autor:
Sofia Barbosa-Gouveia, Maria Eugenia Vázquez-Mosquera, Emiliano González-Vioque, Álvaro Hermida-Ameijeiras, Paula Sánchez-Pintos, Maria José de Castro, Soraya Ramiro León, Belén Gil-Fournier, Cristina Domínguez-González, Ana Camacho Salas, Luis Negrão, Isabel Fineza, Francisco Laranjeira, Maria Luz Couce
Publikováno v:
Journal of Clinical Medicine; Volume 11; Issue 10; Pages: 2750
Neuromuscular diseases are genetically highly heterogeneous, and differential diagnosis can be challenging. Over a 3-year period, we prospectively analyzed 268 pediatric and adult patients with a suspected diagnosis of inherited neuromuscular disorde
Autor:
Ana Teresa Timóteo, Maria Carmo Cachulo, Paulo Dinis, Luís Negrão, Inês Barreiros-Mota, Hélder Dores, Lino Gonçalves
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 43, Iss 6, Pp 301-310 (2024)
Introduction and objectives: Childhood offers an excellent window of opportunity to start interventions to promote behavioral changes before unhealthy lifestyles become established, leading to cardiovascular diseases. The goal of this pilot education
Externí odkaz:
https://doaj.org/article/14c439acc5d946969b1cf54ebb205c1a
Autor:
Luis Negrão, Paula Nunes
Publikováno v:
Pain Management. 6:25-29
Background: Carpal tunnel syndrome is the most common type of peripheral entrapment neuropathy. Patients & methods: We performed an exploratory, open-label, multicenter, observational study of 48 patients with peripheral entrapment neuropathy. Patien
Autor:
Mauro Borghi Moreira da Silva, André Luis Negrão Albanez, Rosa Luiza Moraes Teixeira de Aguiar, Milton Soibelmann Lapchik, Mariela Andrea Cartagena Tapia Borges
Publikováno v:
Anais do Congresso Internacional de Qualidade em Serviços e Sistemas de Saúde.
Autor:
Mariela Andrea Cartagena Tapia Borges, Rosa Luiza Moraes Teixeira de Aguiar, Mauro Borghi Moreira da Silva, Milton Soibelmann Lapchik, André Luis Negrão Albanez
Publikováno v:
Anais do Congresso Internacional de Qualidade em Serviços e Sistemas de Saúde.
Autor:
Ulisses Melo Silva, Ricardo Figueira, Pedro Almeida, Teresa Libório, Luis Negrão, Laura Neto Parra, Sílvia Gonçalves, Helena Duro, Sérgio Alcino
Publikováno v:
Pain Management. 4:191-196
SUMMARY: Aims: Peripheral neuropathy (PN) is a common condition whose incidence is approximately 8% in elderly persons. Neuropathic pain (NeP) has a significant incidence in the general population and affects more than half of all patients with PN. T
Autor:
Ana Inês Martins, Ricardo Soares-dos-Reis, André Jorge, Cristina Duque, Daniela Jardim Pereira, Carlos Fontes Ribeiro, João Sargento-Freitas, Anabela Matos, Luís Negrão, João Lemos
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
IntroductionOculopalatal tremor (OPT) is a late manifestation of a Guillain-Mollaret triangle lesion. Memantine has been shown to improve nystagmus in OPT, but its long-term efficacy and putative distinct effects on each plane of nystagmus and on ass
Externí odkaz:
https://doaj.org/article/a4e621beebb4437693483a718d6a1511
Akademický článek
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Autor:
Inês Sousa, Patrícia Abrantes, Vânia Francisco, Gilberto Teixeira, Marta Monteiro, João Neves, Ana Norte, Carlos Robalo Cordeiro, João Moura E Sá, Ernestina Reis, Patrícia Santos, Manuela Oliveira, Susana Sousa, Marta Fradinho, Filipa Malheiro, Luís Negrão, Salvato Feijó, Sofia A Oliveira
Publikováno v:
PLoS ONE, Vol 11, Iss 5, p e0156103 (2016)
Despite elevated incidence and recurrence rates for Primary Spontaneous Pneumothorax (PSP), little is known about its etiology, and the genetics of idiopathic PSP remains unexplored. To identify genetic variants contributing to sporadic PSP risk, we
Externí odkaz:
https://doaj.org/article/e147678741ff48b6a12d26fadcef9d3f
Autor:
Fátima Saraiva, Dina Rodrigues, Helena Andrade, Luís Negrão, Lino Gonçalves, António Marinho, Luís A. Providência
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 31, Iss 3, Pp 241-245 (2012)
Resumo: A distrofia muscular de Emery Dreifuss tipo 1 (DMED1) é uma doença familiar, com transmissão recessiva ligada ao X, resultante da mutação de uma proteína do invólucro nuclear, a emerina. As manifestações clínicas ocorrem geralmente
Externí odkaz:
https://doaj.org/article/343f728204de4acb8682d7fe1a4b9c0f