Patricia Espinheira Sá Maciel


AuthID: R-000-E14

Confirmed Publications: 191



121
TITLE: ATX-3, CDC-48 and UBXN-5: A new trimolecular complex in Caenorhabditis elegans  Full Text
AUTHORS: Ana Joao Rodrigues ; Andreia Neves Carvalho; Anabela Ferro; Anne Rokla; Garry Corthals; Elsa Logarinho ; Patricia Maciel ;
PUBLISHED: 2009, SOURCE: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, VOLUME: 386, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 10
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
122
TITLE: Developmental disturbances associated with agenesis of the permanent maxillary lateral incisor
AUTHORS: Pinho, T; Maciel, P ; Pollmann, C;
PUBLISHED: 2009, SOURCE: BRITISH DENTAL JOURNAL, VOLUME: 207, ISSUE: 12
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
123
TITLE: Evaluation of CSF neurotransmitters and folate in 25 patients with Rett disorder and effects of treatment  Full Text
AUTHORS: Temudo, T; Rios, M; Prior, C; Carrilho, I; Santos, M; Maciel, P ; Sequeiros, J ; Fonseca, M; Monteiro, J; Cabral, P; Vieira, JP; Ormazabal, A; Artuch, R;
PUBLISHED: 2009, SOURCE: BRAIN & DEVELOPMENT, VOLUME: 31, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
124
TITLE: Mutations in the MECP2 Gene Are Not a Major Cause of Rett Syndrome-Like or Related Neurodevelopmental Phenotype in Male Patients
AUTHORS: Minica Santos; Teresa Temudo; Teresa Kay; Ines Carrilho; Ana Medeira; Helena Cabral; Roseli Gomes; Maria Teresa Lourenco; Margarida Venancio; Eulalia Calado; Ana Moreira; Guiomar Oliveira ; Patricia Maciel ;
PUBLISHED: 2009, SOURCE: JOURNAL OF CHILD NEUROLOGY, VOLUME: 24, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
125
TITLE: Nucleocytoplasmic Shuttling Activity of Ataxin-3  Full Text
AUTHORS: Sandra Macedo Ribeiro ; Luisa Cortes ; Patricia Maciel ; Ana Luisa Carvalho ;
PUBLISHED: 2009, SOURCE: PLOS ONE, VOLUME: 4, ISSUE: 6
INDEXED IN: Scopus WOS
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
126
127
TITLE: Analysis of Highly Conserved Regions of the 3’UTR of MECP2 Gene in Patients with Clinical Diagnosis of Rett Syndrome and Other Disorders Associated with Mental Retardation   Full Text
AUTHORS: Mónica Santos; Jin Yan; Teresa Temudo; Guiomar Oliveira; José Pedro Vieira; Jinong Fen; Steve Sommer; Patrícia Maciel ;
PUBLISHED: 2008, SOURCE: Disease Markers, VOLUME: 24, ISSUE: 6
INDEXED IN: CrossRef
IN MY: ORCID | CIÊNCIAVITAE
128
TITLE: Analysis of highly conserved regions of the 3'UTR of MECP2 gene in patients with clinical diagnosis of Rett syndrome and other disorders associated with mental retardation
AUTHORS: Monica Santos; Jin Yan; Teresa Temudo; Guiomar Oliveira ; Jose Pedro Vieira; Jinong Fen; Steve Sommer; Patrica Maciel ;
PUBLISHED: 2008, SOURCE: DISEASE MARKERS, VOLUME: 24, ISSUE: 6
INDEXED IN: Scopus WOS
IN MY: ORCID | ResearcherID | CIÊNCIAVITAE
129
130
TITLE: Movement disorders in Rett syndrome: An analysis of 60 patients with detected MECP2 mutation and correlation with mutation type  Full Text
AUTHORS: Temudo, T; Ramos, E ; Dias, K; Barbot, C ; Vieira, JP; Moreira, A; Calado, E; Carrilho, I; Oliveira, G ; Levy, A; Fonseca, M; Cabral, A; Cabral, P; Monteiro, JP; Borges, L; Gomes, R; Santos, M; Sequeiros, J ; Maciel, P ;
PUBLISHED: 2008, SOURCE: MOVEMENT DISORDERS, VOLUME: 23, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef Handle
IN MY: ORCID | CIÊNCIAVITAE
Page 13 of 20. Total results: 191.

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