Patricia Espinheira Sá Maciel


AuthID: R-000-E14

Publications Requiring Validation

31
TITLE: Region-Specific Changes in the Expression of Hsp70 in the Central Nervous System of a Transgenic Mouse Model of Machado-Joseph Disease
AUTHORS: Cruto, T; Teixeira Castro, A; Silva Fernandes, A ; Costa, MD; Duarte Silva, S; Maciel, P;
PUBLISHED: 2009, SOURCE: NEUROLOGY, VOLUME: 72, ISSUE: 11
INDEXED IN: WOS
IN MY: ORCID
32
TITLE: Huntington's disease and Huntington-like phenotype: 10 years of local molecular diagnostic experience
AUTHORS: Santos, C; Cerqueira, J; Magalhaes, P; Costa, MC; Jardim, L; Costa, C; Cruz, V ; Coutinho, P; Maciel, P; Sequeiros, J ;
PUBLISHED: 2008, SOURCE: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, VOLUME: 79
INDEXED IN: WOS
IN MY: ORCID
33
TITLE: Genetic study of Portuguese patients with Huntington disease-like phenotype
AUTHORS: Costa, MC; Pereira, MC; Magalhaes, P; Matama, MT; Ferreirinha, F; Cerqueira, J; Santos, MM ; Sequeiros, J ; Maciel, P;
PUBLISHED: 2003, SOURCE: Annual Meeting of the American-Society-of-Human-Genetics in AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 73, ISSUE: 5
INDEXED IN: WOS
IN MY: ORCID
34
TITLE: Association study of multiple sclerosis in Portuguese patients: whole genome screen using 6000 microsatellite markers and a DNA pooling strategy
AUTHORS: Pinto Basto, J; Santos, M; Rio, ME; Valenca, A; Sequeiros, J ; Maciel, P;
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
IN MY: ORCID
35
TITLE: Mutation in the PAX9 gene and absence of mutations in MSX1 gene in Portuguese families with hypodontia.
AUTHORS: Seada, PMP; Pinho, T; Pollman, C; Sequeiros, J ; Tavares, P; Maciel, P;
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
IN MY: ORCID
36
TITLE: Genetic and molecular study of migraine.
AUTHORS: Castro, MJ; Alonso, I; Maciel, P; Sousa, A; Guimaraes, L ; Fraga, C; Barros, José ; Sequeiros, J ; Peieira Monteiro, 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
IN MY: ORCID
37
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
38
TITLE: Frequency of SCA1, DRPLA, MJD, SCA2 and SCA6 mutations in a large group of Portuguese families with spinocerebellar ataxia  Full Text
AUTHORS: Silveira, I; Coutinho, P; Maciel, P; Hayes, S; Dias, A; Guimaraes, J; Loureiro, LL; Barros, José ; Chorao, R; Ribeiro, P; Bettencourt, M; Serrano, P; Silva, C; Rouleau, GA; Sequeiros, J ;
PUBLISHED: 1998, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 6
INDEXED IN: WOS
39
TITLE: An intermediate allele of 51 repeats found at the Machado-Joseph disease (MJD) locus: implications for predictive testing and the study of the origin of MJD mutation.
AUTHORS: Maciel, P; Rousseau, M; Gaspar, C; Coutinho, P; Sequeiros, J ; Rouleau, GA;
PUBLISHED: 1997, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 61, ISSUE: 4
INDEXED IN: WOS
40
TITLE: Frequency of the CAG repeat mutations causing spinocerebellar ataxia in a large group of Portuguese ataxia families.
AUTHORS: Silveira, I; Coutinho, P; Maciel, P; Gaspar, C; Hayes, S; Dias, A; Guimaraes, J; Loureiro, L; Sequeiros, J ; Rouleau, GA;
PUBLISHED: 1997, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 61, ISSUE: 4
INDEXED IN: WOS
Page 4 of 5. Total results: 42.

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