1. Repositório Científico do Centro Hospitalar do Porto

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Issue DateTitleAuthor(s)TypeAccess Type
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
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
Nov-2001Improvement in the molecular diagnosis of Machado-Joseph diseaseMaciel, P.; Costa, M.; Ferro, A.; Rousseau, M.; Santos, C.; Gaspar, C.; Barros, J.; Rouleau, G.; Coutinho, P.; Sequeiros, J.articleopenAccess
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
Jul-2006Cerebellar ataxia with spasmodic cough: a new form of dominant ataxiaCoutinho, P.; Cruz, V.; Tuna, A.; Silva, S.; Guimarães, J.articleopenAccess

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