Ana Isabel Barreira Seixas
AuthID: R-000-JM5
11
TITLE: 'Costa da Morte' ataxia is spinocerebellar ataxia 36: clinical and genetic characterization Full Text
AUTHORS: Garcia-Murias, M; Quintans, B; Arias, M; Seixas, AI; Cacheiro, P; Tarrio, R; Pardo, J; Millan, MJ; Arias-Rivas, S; Blanco-Arias, P; Dapena, D; Moreira, R; Rodriguez-Trelles, F; Sequeiros, J; Carracedo, A; Silveira, I; Sobrido, MJ;
PUBLISHED: 2012, SOURCE: Brain, VOLUME: 135, ISSUE: 5
AUTHORS: Garcia-Murias, M; Quintans, B; Arias, M; Seixas, AI; Cacheiro, P; Tarrio, R; Pardo, J; Millan, MJ; Arias-Rivas, S; Blanco-Arias, P; Dapena, D; Moreira, R; Rodriguez-Trelles, F; Sequeiros, J; Carracedo, A; Silveira, I; Sobrido, MJ;
PUBLISHED: 2012, SOURCE: Brain, VOLUME: 135, ISSUE: 5
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TITLE: FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes Full Text
AUTHORS: Ana I Seixas; Jose Vale; Paula Jorge; Isabel Marques; Rosario Santos; Isabel Alonso ; Ana M Fortuna; Jorge Pinto Basto; Paula Coutinho ; Russell L Margolis; Jorge Sequeiros ; Isabel Silveira ;
PUBLISHED: 2011, SOURCE: BEHAVIORAL AND BRAIN FUNCTIONS, VOLUME: 7, ISSUE: 1
AUTHORS: Ana I Seixas; Jose Vale; Paula Jorge; Isabel Marques; Rosario Santos; Isabel Alonso ; Ana M Fortuna; Jorge Pinto Basto; Paula Coutinho ; Russell L Margolis; Jorge Sequeiros ; Isabel Silveira ;
PUBLISHED: 2011, SOURCE: BEHAVIORAL AND BRAIN FUNCTIONS, VOLUME: 7, ISSUE: 1
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TITLE: A novel trinucleotide repeat expansion at chromosome 3q26.2 identified by a CAG/CTG repeat expansion detection array Full Text
AUTHORS: Holmes, SE; Wentzell, JS; Seixas, AI; Callahan, C; Silveira, I ; Ross, CA; Margolis, RL;
PUBLISHED: 2006, SOURCE: HUMAN GENETICS, VOLUME: 120, ISSUE: 2
AUTHORS: Holmes, SE; Wentzell, JS; Seixas, AI; Callahan, C; Silveira, I ; Ross, CA; Margolis, RL;
PUBLISHED: 2006, SOURCE: HUMAN GENETICS, VOLUME: 120, ISSUE: 2
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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
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
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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
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
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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
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
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TITLE: A novel R1347Q mutation in the predicted voltage sensor segment of the P/Q-type calcium-channel alpha(1A)-subunit in a family with progressive cerebellar ataxia and hemiplegic migraine. Letter to the Editor Full Text
AUTHORS: Alonso, I ; Barros, José ; Tuna, A; Seixas, A; Coutinho, P ; Sequeiros, J ; Silveira, I ;
PUBLISHED: 2004, SOURCE: CLINICAL GENETICS, VOLUME: 65, ISSUE: 1
AUTHORS: Alonso, I ; Barros, José ; Tuna, A; Seixas, A; Coutinho, P ; Sequeiros, J ; Silveira, I ;
PUBLISHED: 2004, SOURCE: CLINICAL GENETICS, VOLUME: 65, ISSUE: 1
