Repositório Científico do Instituto Nacional de Saúde: Browsing DSpace

Issue Date	Title	Author(s)
Nov-2006	Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: no association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene	Correia, C.; Coutinho, A.M.; Diogo, L.; Grazina, M.; Marques, C.; Miguel, T.; Ataíde, A.; Almeida, J.; Borges, L.; Oliveira, C.; Oliveira, G.; Vicente, A.M.
Jun-2009	Characterization of pharmacogenetically relevant CYP2D6 and ABCB1 gene polymorphisms in a Portuguese population sample	Correia, C.; Santos, P.; Coutinho, A.M.; Vicente, A.M.
Oct-2007	Epidemiology of autism spectrum disorder in Portugal: prevalence, clinical characterization, and medical conditions	Oliveira, G.; Ataíde, A.; Marques, C.; Miguel, T.S.; Coutinho, A.M.; Mota-Vieira, L.; Gonçalves, E.; Lopes, N.M.; Rodrigues, V.; Carmona da Mota, H.; Vicente, A.M.
3-Jan-2007	Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels	Coutinho, A.M.; Sousa, I.; Martins, M.; Correia, C.; Morgadinho, T.; Bento, C.; Marques, C.; Ataíde, A.; Miguel, T.S.; Moore, J.H.; Oliveira, G.; Vicente, A.M.
Oct-2010	Increased BDNF levels and NTRK2 gene association suggest a disruption of BDNF/TrkB signaling in autism	Correia, C.T.; Coutinho, A.M.; Sequeira, A.F.; Sousa, I.G.; Lourenço Venda, L.; Almeida, J.P.; Abreu, R.L.; Lobo, C.; Miguel, T.S.; Conroy, J.; Cochrane, L.; Gallagher, L.; Gill, M.; Ennis, S.; Oliveira, G.G.; Vicente, A.M.
5-Jun-2007	MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients	Coutinho, A.M.; Oliveira, G.; Katz, C.; Feng, J.; Yan, J.; Yang, C.; Marques, C.; Ataíde, A.; Miguel, T.S.; Borges, L.; Almeida, J.; Correia, C.; Currais, A.; Bento, C.; Mota-Vieira, L.; Temudo, T.; Santos, M.; Maciel, P.; Sommer, S.S.; Vicente, A.M.

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