Guiomar Gonçalves Oliveira


AuthID: R-000-KD9

Confirmed Publications: 23



11
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
12
TITLE: Atypical stereotypies and vocal tics in Rett syndrome: An illustrative case  Full Text
AUTHORS: Teresa Temudo; Paula Freitas; Jorge Sequeiros ; Patricia Maciel ; Guiomar Oliveira ;
PUBLISHED: 2008, SOURCE: MOVEMENT DISORDERS, VOLUME: 23, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
13
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
14
TITLE: Epidemiology of autism spectrum disorder in Portugal: prevalence, clinical characterization, and medical conditions  Full Text
AUTHORS: Guiomar Oliveira ; Assuncao Ataide; Carla Marques; Teresa S Miguel; Ana Margarida Coutinho; Luisa Mota Vieira ; Esmeralda Goncalver ; Nazare Mendes Lopes ; Vitor Rodrigues; Henrique Carmona da Mota; Astrid Moura Vicente ;
PUBLISHED: 2007, SOURCE: DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, VOLUME: 49, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef: 57
IN MY: ORCID
15
TITLE: Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels  Full Text
AUTHORS: Coutinho, AM; Sousa, I; Martins, M ; Correia, C; Morgadinho, T; Bento, C; Marques, C; Ataide, A; Miguel, TS; Moore, JH; Oliveira, G ; Vicente, AM ;
PUBLISHED: 2007, SOURCE: HUMAN GENETICS, VOLUME: 121, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef Handle
IN MY: ORCID
16
TITLE: MECP2 coding sequence and 3 ' UTR variation in 172 unrelated autistic patients  Full Text
AUTHORS: Ana M Coutinho; Guiomar Oliveira ; Cecile Katz; Jinong N Feng; Jin Yan; Chunmei M Yang; Carla Marques; Assuncao Ataide; Teresa S Miguel; Luis Borges; Joana Ahneida; Catarina Correia; Antonio Currais; Celeste Bento; Luisa Mota Vieira ; Teresa Temudo; Monica Santos; Patricia Maciel ; Steve S Sommer; Astrid M Vicente ;
PUBLISHED: 2007, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, VOLUME: 144B, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
17
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
18
TITLE: Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: No association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene  Full Text
AUTHORS: Catarina Correia; Ana M Coutinho; Luisa Diogo; Manuela Grazina ; Carla Marques; Teresa Miguel; Assuncao Ataide; Joana Almeida; Luis Borges; Catarina Oliveira ; Guiomar Oliveira ; Astrid M Vicente ;
PUBLISHED: 2006, SOURCE: JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, VOLUME: 36, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 52
IN MY: ORCID
19
TITLE: Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients  Full Text
AUTHORS: Yan, J; Oliveira, G ; Coutinho, A; Yang, C; Feng, J; Katz, C; Sram, J; Bockholt, A; Jones, IR; Craddock, N; Cook, EH; Vicente, A ; Sommer, SS;
PUBLISHED: 2005, SOURCE: MOLECULAR PSYCHIATRY, VOLUME: 10, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
20
TITLE: Mitochondrial dysfunction in autism spectrum disorders: a population-based study  Full Text
AUTHORS: Oliveira, G ; Diogo, L; Grazina, M ; Garcia, P; Ataide, A; Marques, C; Miguel, T; Borges, L; Vicente, AM ; Oliveira, CR ;
PUBLISHED: 2005, SOURCE: DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, VOLUME: 47, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 138
IN MY: ORCID
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