Isabel Alexandra Azevedo Silveira


AuthID: R-000-66E

Confirmed Publications: 46



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TITLE: Autosomal Dominant Spastic Paraplegias A Review of 89 Families Resulting From a Portuguese Survey. A Review of 89 Families Resulting From a Portuguese Survey
AUTHORS: Loureiro, JL ; Brandao, E; Ruano, L ; Brandao, AF; Lopes, AM; Thieleke Matos, C; Miller Fleming, L; Cruz, VT ; Barbosa, M; Silveira, I ; Stevanin, G; Pinto Basto, J; Sequeiros, J ; Alonso, I ; Coutinho, P ;
PUBLISHED: 2013, SOURCE: JAMA NEUROLOGY, VOLUME: 70, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 46
IN MY: ORCID
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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
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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
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TITLE: Epidemiology and population genetics of degenerative ataxias
AUTHORS: Sequeiros, J ; Martins, S ; Silveira, I ;
PUBLISHED: 2011, SOURCE: Handbook of Clinical Neurology, VOLUME: 103
INDEXED IN: Scopus CrossRef: 51
IN MY: ORCID
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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: 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
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TITLE: Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal  Full Text
AUTHORS: Vale, J; Bugalho, P; Silveira, I ; Sequeiros, J ; Guimaraes, J; Coutinho, P ;
PUBLISHED: 2010, SOURCE: EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 17, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
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TITLE: Common Origin of Pure and Interrupted Repeat Expansions in Spinocerebellar Ataxia Type 2 (SCA2)  Full Text
AUTHORS: Eliana Marisa Ramos; Sandra Martins ; Isabel Alonso ; Vanessa E Emmel; Maria Luiza Saraiva Pereira; Laura Bannach Jardim; Paula Coutinho ; Jorge Sequeiros ; Isabel Silveira ;
PUBLISHED: 2010, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, VOLUME: 153B, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 28
IN MY: ORCID
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