%0 Journal Article %J Behavioral and Brain Functions %D 2011 %T FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes %A Seixas, A.I. %A Vale, J. %A Jorge, P. %A Marques, I. %A Santos, R. %A Alonso, I. %A Fortuna, A.M. %A Pinto-Basto, J. %A Coutinho, P. %A Margolis, R.L. %A Sequeiros, J. %A Silveira, I. %B Behavioral and Brain Functions %V 7 %8 2011/// %G eng %U http://www.scopus.com/inward/record.url?eid=2-s2.0-79957829884&partnerID=40&md5=2be467541a40dac8980e300ecb23245a %0 Journal Article %J European Journal of Neurology %D 2010 %T Autosomal dominant cerebellar ataxia: Frequency analysis and clinical characterization of 45 families from Portugal %A Vale, J. %A Bugalho, P. %A Silveira, I. %A Sequeiros, J. %A Guimarães, J. %A Coutinho, P. %B European Journal of Neurology %V 17 %P 124 - 128 %8 2010/// %G eng %U http://www.scopus.com/inward/record.url?eid=2-s2.0-73449139787&partnerID=40&md5=d65413d358bdb0682d35f110b8398b03 %N 1 %0 Journal Article %J Journal of Human Genetics %D 2006 %T Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype %A Costa, M.D.C. %A Teixeira-Castro, A. %A Constante, M. %A Magalhães, M. %A Magalhães, P. %A Cerqueira, J. %A Vale, J. %A Passão, V. %A Barbosa, C. %A Robalo, C. %A Coutinho, P. %A Barros, J. %A Santos, M.M. %A Sequeiros, J. %A MacIel, P. %B Journal of Human Genetics %V 51 %P 645 - 651 %8 2006/// %G eng %U http://www.scopus.com/inward/record.url?eid=2-s2.0-77952878970&partnerID=40&md5=06556bbe8033f2aee296c9362b5a1d3a %N 8