ProfileOfResearchers

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

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

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:

ResearcherID

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

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

Handle

IN MY:

ORCID

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

IN MY:

ORCID