Percorrer por autor Costa, M

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DataTítuloAutor(es)TipoAcesso
2013A case of systemic pseudohypoaldosteronism with a novel mutation in the SCNN1A geneSilva, N; Costa, M; Silva, A; Sá, C; Martins, S; Antunes, A; Marques, O; Castedo, S; Pereira, AarticleopenAccess
2012Diagnosing Schmidt Syndrome in AdolescenceCosta, M; Martins, S; Mota, F; Marques, O; Antunes, AarticleopenAccess
2014Novel ABCA3 mutations as a cause of respiratory distress in a term newbornGonçalves, JP; Pinheiro, L; Costa, M; Silva, A; Gonçalves, A; Pereira, AarticleopenAccess
24-Abr-2018Thrombus aspiration in patients with ST-elevation myocardial infarction: results of a national registry of interventional cardiologyPereira, H; Caldeira, D; Teles, RC; Costa, M; da Silva, PC; da Gama Ribeiro, V; Brandão, V; Martins, D; Matias, F; Pereira-Machado, F; Baptista, J; Abreu, PF; Santos, R; Drummond, A; de Carvalho, HC; Calisto, J; Silva, JC; Pipa, JL; Marques, J; Sousa, P; Fernandes, R; Ferreira, RC; Ramos, S; Oliveira, EI; de Sousa Almeida, MarticleopenAccess
5-Jul-2016Trends in coronary angioplasty in Portugal from 2002 to 2013 according to the Portuguese National Registry of Interventional CardiologyPereira, H; Campante Teles, R; Costa, M; Canas da Silva, P; da Gama Ribeiro, V; Brandão, V; Martins, D; Matias, F; Pereira-Machado, F; Baptista, J; Farto E Abreu, P; Santos, R; Drummond, A; Cyrne de Carvalho, H; Calisto, J; Silva, JC; Pipa, JL; Marques, J; Sousa, P; Fernandes, R; Cruz Ferreira, R; Ramos, S; Oliveira, E; Almeida, MarticleopenAccess