151
TITLE: Psychological impact of pre-symptomatic genetic testing for Machado-Joseph disease: preliminary results.  Full Text
AUTHORS: Ledo, S; Fleming, M; Rocha, JC; Sequeiros, J ;
PUBLISHED: 2002, SOURCE: European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 10
INDEXED IN: WOS
152
TITLE: Psychological well-being in individuals requesting pre-symptomatic testing for late-onset neurological diseases and controls  Full Text
AUTHORS: Leite, AMT; Paul, C; Sequeiros, J ;
PUBLISHED: 2002, SOURCE: European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 10
INDEXED IN: WOS
153
TITLE: Regions of instability and mutability at the SCA8 locus.
AUTHORS: Martins, S ; Magalhaes, P; Alonso, L; Sequeiros, J ; Silveira, I;
PUBLISHED: 2002, SOURCE: 52nd Annual Meeting of the American-Society-of-Human-Genetics in AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 71, ISSUE: 4
INDEXED IN: WOS
154
TITLE: Study of the normal CAG tract at the Huntington disease locus in the Portuguese population  Full Text
AUTHORS: Costa, MC; Guimaraes, L ; Ferreirinha, F; Sousa, A; Maciel, P; Sequeiros, J ;
PUBLISHED: 2002, SOURCE: European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 10
INDEXED IN: WOS
155
TITLE: Susceptibility and disease progression in Portuguese patients with multiple sclerosis - study of the role of APOE and SCA2 loci  Full Text
AUTHORS: Santos, M; Costa, MC; Rio, ME; Sa, MJ; Monteiro, M; Valenca, A; Sa, A; Dinis, J; Figueiredo, J; de Almeida, LB; Valongueiro, A; Coelho, I; Matama, MT; Pinto Basto, J; Sequeiros, J ; Maciel, P;
PUBLISHED: 2002, SOURCE: European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 10
INDEXED IN: WOS
156
TITLE: Trinucleotide repeats in 202 families with ataxia - A small expanded (CAG)(n) allele at the SCA17 locus. A Small Expanded (CAG) n Allele at the SCA17 Locus
AUTHORS: Silveira, I ; Miranda, C; Guimaraes, L ; Moreira, MC; Alonso, I ; Mendonca, P; Ferro, A; Pinto Basto, J; Coelho, J; Ferreirinha, F ; Poirier, J; Parreira, E; Vale, J; Januario, C; Barbot, C ; Tuna, A; Barros, José ; Koide, R; Tsuji, S; Holmes, SE; Margolis, RL; Jardim, L; Pandolfo, M; Coutinho, P ; Sequeiros, J ; ...More
PUBLISHED: 2002, SOURCE: ARCHIVES OF NEUROLOGY, VOLUME: 59, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 127
IN MY: ORCID
157
TITLE: Triplet repeat sizes in candidate genes for Spinocerebellar ataxia.
AUTHORS: Homem, C; Magalhaes, P; Sequeiros, J ; Silveira, I;
PUBLISHED: 2002, SOURCE: 52nd Annual Meeting of the American-Society-of-Human-Genetics in AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 71, ISSUE: 4
INDEXED IN: WOS
158
TITLE: A missense mutation in a calcium-channel gene causes SCA in a four generation family also with hemiplegic migraine.
AUTHORS: Alonso, I; Tuna, A; Coelho, J; Barros, José ; Sequeiros, J ; Silveira, I; Coutinho, P;
PUBLISHED: 2001, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 69, ISSUE: 4
INDEXED IN: WOS
159
TITLE: A survey of spinocerebellar ataxia in South Brazil - 66 new cases with Machado-Joseph disease, SCA7, SCA8, or unidentified disease - Causing mutations  Full Text
AUTHORS: Jardim, LB; Silveira, I ; Pereira, ML; Ferro, A; Alonso, I ; Moreira, MDC; Mendonca, P; Ferreirinha, F ; Sequeiros, J ; Giugliani, R;
PUBLISHED: 2001, SOURCE: JOURNAL OF NEUROLOGY, VOLUME: 248, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef: 72
IN MY: ORCID
160
TITLE: Ancestral origins of the Machado-Joseph disease mutation: A worldwide haplotype study
AUTHORS: Gaspar, C; Lopes Cendes, I; Hayes, S; Goto, J; Arvidsson, K; Dias, A; Silveira, I ; Maciel, P ; Coutinho, P ; Lima, M ; Zhou, YX; Soong, BW; Watanabe, M; Giunti, P; Stevanin, G; Riess, O; Sasaki, H; Hsieh, M; Nicholson, GA; Brunt, E; Higgins, JJ; Lauritzen, M; Tranebjaerg, L; Volpini, V; Wood, N; Ranum, L; Tsuji, S; Brice, A; Sequeiros, J ; Rouleau, GA; ...More
PUBLISHED: 2001, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 68, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef
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