Patricia Espinheira Sá Maciel


AuthID: R-000-E14

Confirmed Publications: 191



141
TITLE: NEDD8: A new ataxin-3 interactor  Full Text
AUTHORS: Ferro, A; Carvalho, AL ; Teixeira Castro, A ; Almeida, C; Tome, RJ; Cortes, L ; Rodrigues, AJ ; Logarinho, E ; Sequeiros, J ; Macedo Ribeiro, S ; Maciel, P ;
PUBLISHED: 2007, SOURCE: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, VOLUME: 1773, ISSUE: 11
INDEXED IN: Scopus WOS CrossRef Handle
IN MY: ORCID | CIÊNCIAVITAE
142
143
TITLE: Stereotypies in Rett syndrome - Analysis of 83 patients with and without detected MECP2 mutations
AUTHORS: Temudo, T; Oliveira, P ; Santos, M; Dias, K; Vieira, J; Moreira, A; Calado, E; Carrilho, I; Oliveira, G ; Levy, A; Barbot, C ; Fonseca, M; Cabral, A; Dias, A; Cabral, P; Monteiro, J; Borges, L; Gomes, R; Barbosa, C; Mira, G; Eusebio, F; Santos, M; Sequeiros, J ; Maciel, P ; ...More
PUBLISHED: 2007, SOURCE: NEUROLOGY, VOLUME: 68, ISSUE: 15
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
144
145
TITLE: APOE epsilon variation in multiple sclerosis susceptibility and disease severity - Some answers
AUTHORS: Burwick, RM; Ramsay, PP; Haines, JL; Hauser, SL; Oksenberg, JR; Pericak Vance, MA; Schmidt, S; Compston, A; Sawcer, S; Cittadella, R; Savettieri, G; Quattrone, A; Polman, CH; Uitdehaag, BMJ; Zwemmer, JNP; Hawkins, P; Ollier, WER; Weatherby, S; Enzinger, C; Fazekas, F; Schmidt, H; Schmidt, R; Hillert, J; Masterman, T; Hogh, P; Niino, M; Kikuchi, S; Maciel, P ; Santos, M; Rio, ME; Kwiecinski, H; Zakrzewska Pniewska, B; Evangelou, N; Palace, J; Barcellos, LF; ...More
PUBLISHED: 2006, SOURCE: NEUROLOGY, VOLUME: 66, ISSUE: 9
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
146
TITLE: Chromatin remodeling and neuronal function: exciting links
AUTHORS: Santos, M; Coelho, PA; Maciel, P ;
PUBLISHED: 2006, SOURCE: GENES BRAIN AND BEHAVIOR, VOLUME: 5
INDEXED IN: WOS
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
147
TITLE: Chromatin remodeling and neuronal function: Exciting links  Full Text
AUTHORS: Santos, M; Coelho, PA; Maciel, P ;
PUBLISHED: 2006, SOURCE: Genes, Brain and Behavior, VOLUME: 5, ISSUE: SUPPL. 2
INDEXED IN: Scopus CrossRef
IN MY: ORCID | CIÊNCIAVITAE
148
TITLE: Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype  Full Text
AUTHORS: Maria do Carmo Costa; Andreia Teixeira Castro ; Marco Constante; Marina Magalhaes; Paula Magalhaes; Joana Cerqueira; Jose Vale; Vitorina Passao; Celia Barbosa; Conceicao Robalo; Paula Coutinho ; Barros, José ; Manuela M Santos; Jorge Sequeiros ; Patricia Maciel ;
PUBLISHED: 2006, SOURCE: JOURNAL OF HUMAN GENETICS, VOLUME: 51, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID | CIÊNCIAVITAE
149
TITLE: The CAG repeat at the Huntington disease gene in the Portuguese population: insights into its dynamics and to the origin of the mutation
AUTHORS: Costa, MD; Magalhaes, P; Guimaraes, L ; Maciel, P ; Sequeiros, J ; Sousa, A ;
PUBLISHED: 2006, SOURCE: JOURNAL OF HUMAN GENETICS, VOLUME: 51, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 32 Handle
IN MY: ORCID | CIÊNCIAVITAE
150
TITLE: Detection of heterozygous deletions and duplications in the MECP2 gene in Rett syndrome by Robust Dosage PCR (RD-PCR)  Full Text
AUTHORS: Jinxiu Shi; Akane Shibayama; Qiang Liu; Vu Q Nguyen; Jinong Feng; M�nica Santos; Teresa Temudo; Patricia Maciel ; Steve S Sommer;
PUBLISHED: 2005, SOURCE: Human Mutation - Hum. Mutat., VOLUME: 25, ISSUE: 5
INDEXED IN: CrossRef
IN MY: ORCID | CIÊNCIAVITAE
Page 15 of 20. Total results: 191.

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