@article {3111, title = {FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes}, journal = {Behavioral and Brain Functions}, volume = {7}, year = {2011}, note = {Export Date: 18 March 2013Source: ScopusArt. No.: 19}, month = {2011///}, url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-79957829884\&partnerID=40\&md5=2be467541a40dac8980e300ecb23245a}, author = {Seixas, A.I. and Vale, J. and Jorge, P. and Marques, I. and Santos, R. and Alonso, I. and Fortuna, A.M. and Pinto-Basto, J. and Coutinho, P. and Margolis, R.L. and Sequeiros, J. and Silveira, I.} } @article {3367, title = {Autosomal dominant cerebellar ataxia: Frequency analysis and clinical characterization of 45 families from Portugal}, journal = {European Journal of Neurology}, volume = {17}, year = {2010}, note = {Cited By (since 1996): 6Export Date: 18 March 2013Source: Scopus}, month = {2010///}, pages = {124 - 128}, url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-73449139787\&partnerID=40\&md5=d65413d358bdb0682d35f110b8398b03}, author = {Vale, J. and Bugalho, P. and Silveira, I. and Sequeiros, J. and Guimar{\~a}es, J. and Coutinho, P.} } @article {4015, title = {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}, journal = {Journal of Human Genetics}, volume = {51}, year = {2006}, note = {Cited By (since 1996): 13Export Date: 18 March 2013Source: Scopus}, month = {2006///}, pages = {645 - 651}, url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-77952878970\&partnerID=40\&md5=06556bbe8033f2aee296c9362b5a1d3a}, author = {Costa, M.D.C. and Teixeira-Castro, A. and Constante, M. and Magalh{\~a}es, M. and Magalh{\~a}es, P. and Cerqueira, J. and Vale, J. and Pass{\~a}o, V. and Barbosa, C. and Robalo, C. and Coutinho, P. and Barros, J. and Santos, M.M. and Sequeiros, J. and MacIel, P.} }