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1
المؤلفون: Audrey Romano, Nicolas Duflot, Ana M. Coutinho, Narcis Kabaterene, Christopher Kenneth Opio, Valéria Rêgo Alves Pereira, Carla Mola, Alain Dessein, Hélia Dessein
المصدر: Human Genetics. 139:833-833
مصطلحات موضوعية: musculoskeletal diseases, Published Erratum, MEDLINE, Biology, Bioinformatics, medicine.disease, Molecular medicine, Human genetics, stomatognathic diseases, Liver disease, immune system diseases, Genetics, medicine, skin and connective tissue diseases, Genetics (clinical)
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2
المؤلفون: Guiomar Oliveira, Assunção Ataíde, C.C. Marques, Ana M. Coutinho, Teresa S. Miguel, Jason H. Moore, Teresa Morgadinho, Inês Sousa, Catarina Correia, Astrid M. Vicente, Madalena Martins, Celeste Bento
المصدر: Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAPمصطلحات موضوعية: Blood Platelets, Male, Serotonin, Candidate gene, Adolescent, Biology, Linkage Disequilibrium, 03 medical and health sciences, 0302 clinical medicine, Neurodevelopmental disorder, Genetics, medicine, Humans, Genetic Predisposition to Disease, Heritability of autism, Autistic Disorder, Child, Genetics (clinical), 030304 developmental biology, Serotonin Plasma Membrane Transport Proteins, 0303 health sciences, TPH1, Haplotype, Integrin beta3, Epistasis, Genetic, Transmission disequilibrium test, medicine.disease, Developmental disorder, Haplotypes, Child, Preschool, Perturbações do Desenvolvimento Infantil e Saúde Mental, Autism, Female, 030217 neurology & neurosurgery
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3
المؤلفون: Luís Borges, Assunção Ataíde, Joana Almeida, Astrid M. Vicente, Ana M. Coutinho, C.C. Marques, Manuela Grazina, Catarina R. Oliveira, Luísa Diogo, Guiomar Oliveira, Teresa S. Miguel, Catarina Correia
المصدر: Journal of Autism and Developmental Disorders. 36:1137-1140
مصطلحات موضوعية: medicine.medical_specialty, Mitochondrial Diseases, DNA Mutational Analysis, Gene Expression, Glutamic Acid, Mitochondrion, DNA, Mitochondrial, Mitochondrial Membrane Transport Proteins, Genetic determinism, Mitochondrial Proteins, Gene Frequency, Internal medicine, Pyruvic Acid, Developmental and Educational Psychology, medicine, Glutamate aspartate transporter, Humans, Lactic Acid, Autistic Disorder, Gene, DNA Primers, Aspartic Acid, biology, Metabolic disorder, Glutamate receptor, Chromosome Mapping, Membrane Transport Proteins, medicine.disease, Developmental disorder, Endocrinology, Haplotypes, biology.protein, Autism, Psychology
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4
المؤلفون: Ana M. Coutinho, Constantin Fesel, Susana C Silva, Astrid M. Vicente, C.C. Marques, Celeste Bento, Guiomar Oliveira, Marta Barreto, Assunção Ataíde, Luís Borges, Catarina Correia, Teresa S. Miguel
المصدر: Journal of Neuroimmunology. 152:176-182
مصطلحات موضوعية: Male, Adolescent, Blotting, Western, Immunology, medicine.disease_cause, Neuroprotection, Nuclear Family, Autoimmunity, Pathogenesis, Immune system, Antigen, medicine, Humans, Immunology and Allergy, Autistic Disorder, Child, Autoantibodies, biology, Autoantibody, Brain, Myelin Basic Protein, medicine.disease, Myelin basic protein, Neurology, Child, Preschool, biology.protein, Autism, Female, Neurology (clinical), Neuroscience
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5
المؤلفون: Madalena Martins, Michael Gill, Catarina Correia, Judith Conroy, Joana R. Almeida, Raquel Lontro, Teresa S. Miguel, Cristina Lobo, Louise Gallagher, Guiomar Oliveira, Astrid M. Vicente, Ana M. Coutinho
المصدر: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. (8)
مصطلحات موضوعية: Genetic Markers, Genetic Linkage, Neuroimmunomodulation, Autism, Integrin alpha4, Population, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Cellular and Molecular Neuroscience, medicine, SNP, Humans, Heritability of autism, Neuroimmune process, Allele, Autistic Disorder, education, Genetics (clinical), Genetic Association Studies, Genetic association, Autoantibodies, Genetics, Family Health, education.field_of_study, Brain, medicine.disease, Developmental disorder, Psychiatry and Mental health, Chromosomes, Human, Pair 2, ITGA4 gene, Perturbações do Desenvolvimento Infantil e Saúde Mental, Neurogenic Inflammation
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6
المؤلفون: Ana M. Coutinho, Guiomar Oliveira, Assunção Ataíde, Teresa S. Miguel, Henrique Carmona da Mota, Vitor Rodrigues, Luisa Mota-Vieira, Astrid M. Vicente, Esmeralda Gonçalves, C.C. Marques, Nazaré Mendes Lopes
المصدر: Developmental medicine and child neurology. 49(10)
مصطلحات موضوعية: Male, medicine.medical_specialty, Mitochondrial Diseases, Severity of Illness Index, Epidemiology of autism, Fragile X Mental Retardation Protein, Developmental Neuroscience, Surveys and Questionnaires, Epidemiology, medicine, Prevalence, Humans, Mass Screening, Point Mutation, Spectrum disorder, Autistic Disorder, Psychiatry, Child, Mass screening, In Situ Hybridization, Chromosomes, Human, Pair 15, Portugal, business.industry, Incidence (epidemiology), medicine.disease, Mitochondrial respiratory chain, Socioeconomic Factors, Karyotyping, Perturbações do Desenvolvimento Infantil e Saúde Mental, Pediatrics, Perinatology and Child Health, Childhood Autism Rating Scale, Autism, Female, Neurology (clinical), business, Gene Deletion
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7
المؤلفون: Mónica Santos, Celeste Bento, Steve S. Sommer, Joana Almeida, Patrícia Maciel, Astrid M. Vicente, Ana M. Coutinho, Luís Borges, C.C. Marques, Jin Yan, Cécile Katz, Teresa Temudo, Guiomar Oliveira, Luisa Mota-Vieira, Jinong Feng, Assunção Ataíde, Chunmei Yang, Catarina Correia, Antonio Currais, Teresa S. Miguel
المساهمون: Universidade do Minho
المصدر: Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAPمصطلحات موضوعية: Male, Methyl-CpG-Binding Protein 2, Autism, DNA Mutational Analysis, Medicina Básica [Ciências Médicas], medicine.disease_cause, Detection of Virtually All Mutations-SSCP, Exon, 0302 clinical medicine, exon 1, X Chromosome Inactivation, Missense mutation, Coding region, Child, Detection of Virtually All Mutations‐SSCP, 3' Untranslated Regions, Genetics (clinical), Genetics, 0303 health sciences, education.field_of_study, Mutation, Alanine, Exons, Pedigree, MECP2, Psychiatry and Mental health, Child, Preschool, Ciências Médicas::Medicina Básica, Female, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, Population, Glycine, Mutation, Missense, Rett syndrome, Biology, 3′UTR, 03 medical and health sciences, Cellular and Molecular Neuroscience, Open Reading Frames, medicine, Humans, RNA, Messenger, Autistic Disorder, education, 030304 developmental biology, Science & Technology, medicine.disease, Introns, Developmental disorder, Gene Expression Regulation, Case-Control Studies, Perturbações do Desenvolvimento Infantil e Saúde Mental, 030217 neurology & neurosurgery
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30df03d031a3b6204a9f4c975af16e58