Guiomar Oliveira
Oliveira, Guiomar Gonçalves de
VIAF ID: 99010115 (Personal)
Permalink: http://viaf.org/viaf/99010115
Preferred Forms
- 100 0 _ ‡a Guiomar Oliveira
- 100 1 _ ‡a Oliveira, Guiomar Gonçalves de
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4xx's: Alternate Name Forms (5)
Works
Title | Sources |
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A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia. | |
Association of the alpha4 integrin subunit gene (ITGA4) with autism. | |
Atypical stereotypies and vocal tics in Rett syndrome: An illustrative case | |
[Autism and Early Neurodevelopmental Milestones]. | |
The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses | |
Autoantibody repertoires to brain tissue in autism nuclear families | |
Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: no association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene. | |
CNVs leading to fusion transcripts in individuals with autism spectrum disorder | |
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders | |
Definition of a putative pathological region in PARK2 associated with autism spectrum disorder through in silico analysis of its functional structure. | |
Dysfunction of the Heteromeric KV7.3/KV7.5 Potassium Channel is Associated with Autism Spectrum Disorders | |
Effectiveness of cochlear implants in children: long term results | |
Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels. | |
A Feasibility Clinical Trial to Improve Social Attention in Autistic Spectrum Disorder (ASD) Using a Brain Computer Interface | |
Functional impact of global rare copy number variation in autism spectrum disorders | |
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders | |
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs | |
A genome-wide scan for common alleles affecting risk for autism | |
Identification of biological mechanisms underlying a multidimensional ASD phenotype using machine learning: Additional file | |
Increased BDNF levels and NTRK2 gene association suggest a disruption of BDNF/TrkB signaling in autism. | |
Individual common variants exert weak effects on the risk for autism spectrum disorders | |
Lições de pediatria | |
Maternal Interactive Behaviours in Parenting Children with Williams Syndrome and Autism Spectrum Disorder: Relations with Emotional/Behavioural Problems | |
MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients. | |
Medial Frontal Lobe Neurochemistry in Autism Spectrum Disorder is Marked by Reduced N-Acetylaspartate and Unchanged Gamma-Aminobutyric Acid and Glutamate + Glutamine Levels. | |
MLPA analysis in a cohort of patients with autism | |
Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 --> qter) detected in an autistic boy. | |
Multidimensional Strategy Regarding the Reduction of Central-Line Associated Infection in Pediatric Intensive Care | |
[Neonatal Morbidity and Gestational Diabetes: Coincidence or Consequence of the 2011 Protocol]. | |
[Neurodevelopmental Outcomes of Very Preterm or Very Low Birth Weigth Infants: Comparison of Monochorionic and Dichorionic Twins with Singletons]. | |
A Novel Biomarker of Compensatory Recruitment of Face Emotional Imagery Networks in Autism Spectrum Disorder | |
Novel personalized therapies for cystic fibrosis in a paediatric population | |
Perturbação do espectro do autismo abordagem clínica e etiológica numa população portuguesa | |
Perturbações do neurodesenvolvimento estado da arte na etiologia e intervenção livro de resumos e programa científico | |
Pharmacogenetics of risperidone therapy in autism: association analysis of eight candidate genes with drug efficacy and adverse drug reactions. | |
Preserved face inversion effects in adults with autism spectrum disorder: an event-related potential study | |
Protein interaction networks reveal novel autism risk genes within GWAS statistical noise | |
Qualidade da vinculação em crianças com perturbações do espectro do autismo contributos individuais, relacionais e clínicos | |
Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders | |
Relatório pedagógico [da] unidade curricular pediatria I | |
REMOVED: Identification of novel genetic causes of Rett syndrome-like phenotypes by whole exome sequencing | |
Rett syndrome with and without detected MECP2 mutations: an attempt to redefine phenotypes. | |
A role for gene-environment interactions in Autism Spectrum Disorder is suggested by variants in genes regulating exposure to environmental factors: Supplementary table 4 | |
Stereotypies in autism spectrum disorder prevalence, clinical determinants, and kinematic analysis | |
Testing a specific link between executive functions and social cognition in autism spectrum disorders | |
Use of early intervention for young children with autism spectrum disorder across Europe. | |
Variants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autism |