1. Repositório Científico do Centro Hospitalar do Porto

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Issue DateTitleAuthor(s)TypeAccess Type
Apr-2003Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large familyAlonso, I.; Barros, J.; Tuna, A.; Coelho, J.; Sequeira, J.; Silveira, I.; Coutinho, P.articleopenAccess
2007Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraineCastro, M.; Stam, A.; Lemos, C.; Barros, J.; Gouveia, R.; Martins, I.; Koenderink, R.; Vanmolkot, K.; Mendes, A.; Frants, R.; Ferrari, M.; Sequeiros, J.; Pereira-Monteiro, J.; van den Maagdenberg, A.articleopenAccess
Feb-2001Homozygosity mapping of Portuguese and Japanese forms of ataxia-oculomotor apraxia to 9p13, and evidence for genetic heterogeneity.Moreira, M.; Barbot, C.; Tachi, N.; Kozuka, N.; Mendonça, P.; Barros, J.; Coutinho, P.; Sequeiros, J.; Koenig, M.articleopenAccess
2012Migraine-induced epistaxis and sporadic hemiplegic migraine: unusual features in the same patientBarros, J.; Damásio, J.; Tuna, A.; Pereira-Monteiro, J.articleopenAccess
Jun-2012Psychotic aura symptoms in familial hemiplegic migraine type 2 (ATP1A2)Barros, J.; Mendes, A.; Matos, I.; Pereira-Monteiro, J.articleopenAccess
1999Clinical Heterogeneity of Autosomal Recessive Spastic Paraplegias: Analysis of 106 Patients in 46 FamiliesCoutinho, P.; Barros, J.; Zemmouri, R.; Guimarães, J.; Alves, C.; Chorão, R.; Lourenço, E.; Ribeiro, P.; Loureiro, J.; Santos, J.; Hamri, A.; Paternotte, C.; Hazan, J.; Silva, M.; Prud'homme, F.; Grid, D.articleopenAccess
16-Sep-2013Monozygotic twin sisters discordant for familial hemiplegic migraineBarros, J.; Barreto, R.; Brandão, A.; Domingos, J.; Damásio, J.; Ramos, C.; Lemos, C.; Sequeiros, J.; Alonso, I.; Pereira-Monteiro, J.articleopenAccess
21-Nov-2012Assessing risk factors for migraine: differences in gender transmissionLemos, C.; Alonso, I.; Barros, J.; Sequeiros, J.; Pereira-Monteiro, J.; Mendonça, D.; Sousa, A.articleopenAccess
Mar-2000High germinal instability of the (CTG)n at the SCA8 locus of both expanded and normal allelesSilveira, I.; Afonso, I.; Guimarães, L.; Mendonça, P.; Santos, C.; Maciel, P.; Matos, J.; Costa, M.; Barbot, C.; Tuna, A.; Barros, J.; Jardim, L.; Coutinho, P.; Sequeiros, J.articleopenAccess
Feb-2001Recessive ataxia with ocular apraxia: review of 22 Portuguese patients.Barbot, C.; Coutinho, P.; Chorão, R.; Ferreira, C.; Barros, J.; Fineza, I.; Dias, K.; Monteiro, J.; Guimarães, A.; Mendonça, P.; Moreira, M.; Sequeiros, J.articleopenAccess

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