41
TITLE: Neurodevelopment milestone abnormalities in rats exposed to stress in early life  Full Text
AUTHORS: Mesquita, AR ; Pego, JM ; Summavielle, T ; Maciel, P ; Almeida, OFX; Sousa, N ;
PUBLISHED: 2007, SOURCE: NEUROSCIENCE, VOLUME: 147, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef
42
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
43
TITLE: Study of disease-relevant polymorphisms in the TLR4 and TLR9 genes: A novel method applied to the analysis of the Portuguese population  Full Text
AUTHORS: Carvalho, A; Marques, A; Maciel, P ; Rodrigues, F ;
PUBLISHED: 2007, SOURCE: MOLECULAR AND CELLULAR PROBES, VOLUME: 21, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 23
44
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
45
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
46
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
47
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
49
TITLE: Detection of heterozygous deletions and duplications in the MECP2 gene in Rett syndrome by Robust Dosage PCR (RD-PCR).
AUTHORS: Shi, J; Shibayama, A; Liu, Q; Nguyen, VQ; Feng, J; Santos, M; Temudo, T; Maciel, P ; Sommer, SS;
PUBLISHED: 2005, SOURCE: Human mutation., VOLUME: 25, ISSUE: 5
INDEXED IN: Scopus
50
TITLE: Developmental absence of maxillary lateral incisors in the Portuguese population
AUTHORS: Pinho, T; Tavares, P; Maciel, P ; Pollmann, C;
PUBLISHED: 2005, SOURCE: EUROPEAN JOURNAL OF ORTHODONTICS, VOLUME: 27, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef
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