Isabel Alexandra Azevedo Silveira


AuthID: R-000-66E

Confirmed Publications: 46



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TITLE: Spinocerebellar ataxias in 114 Brazilian families: clinical and molecular findings  Full Text
AUTHORS: Trott, A; Jardim, LB; Ludwig, HT; Saute, JAM; Artigalas, O; Kieling, C; Wanderley, HYC; Rieder, CRM; Monte, TL; Socal, M; Alonso, I ; Ferro, A; Carvalho, T; do Ceu Moreira, M; Mendonca, P; Ferreirinha, F ; Silveira, I ; Sequeiros, J ; Giugliani, R; Saraiva Pereira, ML;
PUBLISHED: 2006, SOURCE: CLINICAL GENETICS, VOLUME: 70, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 22
IN MY: ORCID
22
TITLE: A novel H101Q mutation causes PKC gamma loss in spinocerebellar ataxia type 14  Full Text
AUTHORS: Alonso, I ; Costa, C; Gomes, A; Ferro, A; Seixas, AI; Silva, S; Cruz, VT ; Coutinho, P ; Sequeiros, J ; Silveira, I ;
PUBLISHED: 2005, SOURCE: JOURNAL OF HUMAN GENETICS, VOLUME: 50, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef: 30
IN MY: ORCID
23
TITLE: FXTAS, SCA10, and SCA17 in American patients with movement disorders  Full Text
AUTHORS: Seixas, AI; Maurer, MH; Lin, M; Callahan, C; Ahuja, A; Matsuura, T; Ross, CA; Hisama, FM; Silveira, I ; Margolis, RL;
PUBLISHED: 2005, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 136A, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
24
TITLE: Haplotype diversity and somatic instability in normal and expanded SCA8 alleles  Full Text
AUTHORS: Martins, S ; Seixas, AI; Magalhaes, P; Coutinho, P ; Sequeiros, J ; Silveira, I ;
PUBLISHED: 2005, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, VOLUME: 139B, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 8
IN MY: ORCID
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TITLE: Portuguese families with dentatorubropallidoluysian atrophy (DRPLA) share a common haplotype of Asian origin  Full Text
AUTHORS: Martins, S ; Matama, T ; Guimaraes, L ; Vale, J; Guimaraes, J; Ramos, L; Coutinho, P ; Sequeiros, J ; Silveira, I ;
PUBLISHED: 2003, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 11, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef: 26
IN MY: ORCID
28
TITLE: Searching for modulating effects of SCA2, SCA6 and DRPLA CAG tracts on the Machado-Joseph disease (SCA3) phenotype  Full Text
AUTHORS: Jardim, L; Silveira, I ; Pereira, ML; Moreira, MD; Mendonca, P; Sequeiros, J ; Giugliani, R;
PUBLISHED: 2003, SOURCE: ACTA NEUROLOGICA SCANDINAVICA, VOLUME: 107, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
29
TITLE: Use of fluoxetine for treatment of Machado-Joseph disease: an open-label study  Full Text
AUTHORS: Monte, TL; Rieder, CRM; Tort, AB; Rockenback, I; Pereira, ML; Silveira, I ; Ferro, A; Sequeiros, J ; Jardim, LB;
PUBLISHED: 2003, SOURCE: ACTA NEUROLOGICA SCANDINAVICA, VOLUME: 107, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
30
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: 126
IN MY: ORCID
Página 3 de 5. Total de resultados: 46.

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