11
TITLE: 'Costa da Morte' ataxia is spinocerebellar ataxia 36: clinical and genetic characterization  Full Text
AUTHORS: Maria Garcia Murias; Beatriz Quintans; Manuel Arias; Ana I Seixas; Pilar Cacheiro; Rosa Tarrio; Julio Pardo; Maria J Millan; Susana Arias Rivas; Patricia Blanco Arias; Dolores Dapena; Ramon Moreira; Francisco Rodriguez Trelles; Jorge Sequeiros ; Angel Carracedo; Isabel Silveira ; Maria J Sobrido;
PUBLISHED: 2012, SOURCE: BRAIN, VOLUME: 135, ISSUE: 5
INDEXED IN: Scopus WOS
IN MY: ORCID
12
TITLE: Loss of junctophilin-3 contributes to huntington disease-like 2 pathogenesis  Full Text
AUTHORS: Ana I Seixas; Susan E Holmes; Hiroshi Takeshima; Amira Pavlovich; Nancy Sachs; Jennifer L Pruitt; Isabel Silveira ; Christopher A Ross; Russell L Margolis; Dobrila D Rudnicki;
PUBLISHED: 2012, SOURCE: ANNALS OF NEUROLOGY, VOLUME: 71, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
13
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
INDEXED IN: CrossRef
IN MY: ORCID
14
TITLE: FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes  Full Text
AUTHORS: Seixas, AI; Vale, J; Jorge, P; Marques, I; Santos, R; Alonso, I ; Fortuna, AM; Pinto Basto, J; Coutinho, P ; Margolis, RL; Sequeiros, J ; Silveira, I ;
PUBLISHED: 2011, SOURCE: BEHAVIORAL AND BRAIN FUNCTIONS, VOLUME: 7, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef Handle
IN MY: ORCID
15
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
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
16
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
17
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
18
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
Page 2 of 2. Total results: 19.