Autism spectrum disorders: the quest for genetic syndromes.
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Zebrafish as an emerging model for studying complex brain disordersAutism spectrum disorders and neuropathology of the cerebellumAdvancing the understanding of autism disease mechanisms through geneticsAcute stress in adulthood impoverishes social choices and triggers aggressiveness in preclinical models.Zebrafish models for translational neuroscience research: from tank to bedside.Merging data from genetic and epigenetic approaches to better understand autistic spectrum disorder.Modulation of GABAergic transmission in development and neurodevelopmental disorders: investigating physiology and pathology to gain therapeutic perspectives.Clinical and autoimmune features of a patient with autism spectrum disorder seropositive for anti-NMDA-receptor autoantibodyRisk factors in autism: Thinking outside the brain.GABAA receptor subunit gene polymorphisms predict symptom-based and developmental deficits in Chinese Han children and adolescents with autistic spectrum disordersAutism spectrum disorder and epileptic encephalopathy: common causes, many questions.Genetic analysis of GABRB3 as a candidate gene of autism spectrum disordersAutism traits in the RASopathies.Integrative Variation Analysis Reveals that a Complex Genotype May Specify Phenotype in Siblings with Syndromic Autism Spectrum Disorder.Candidate Biomarkers in Children with Autism Spectrum Disorder: A Review of MRI Studies.Mutations in JMJD1C are involved in Rett syndrome and intellectual disability.A developmental, longitudinal investigation of autism phenotypic profiles in fragile X syndrome.Biomarkers in autism spectrum disorder: the old and the new.Cutaneous Disease in Autism Spectrum Disorder: A Review.The dopamine transporter role in psychiatric phenotypes.Epigenetics of Autism Spectrum Disorder.Epigenetic Treatment of Neuropsychiatric Disorders: Autism and Schizophrenia.Autism and chromosome abnormalities-A review.Mavoglurant in fragile X syndrome: Results of two randomized, double-blind, placebo-controlled trials.Expanded DMPK repeats in dizygotic twins referred for diagnosis of autism versus absence of expanded DMPK repeats at screening of 330 children with autism.Ventriculomegaly in very-low-birthweight infants with Down syndrome.Comorbidity of intellectual disability confounds ascertainment of autism: implications for genetic diagnosis.Fragile X syndrome and fragile X-associated disorders.Autism-associated Dyrk1a truncation mutants impair neuronal dendritic and spine growth and interfere with postnatal cortical development.Analysis of Extracellular Nucleotide Metabolism in Adult Zebrafish After Embryological Exposure to Valproic Acid.Autism spectrum disorder traits in Slc9a9 knock-out mice.Aberrant tryptophan metabolism: the unifying biochemical basis for autism spectrum disorders?Phelan-McDermid syndrome presenting with autistic spectrum: are we underdiagnosing chromosomal diseases in patients with autism?
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Autism spectrum disorders: the quest for genetic syndromes.
description
article científic
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article scientifique
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articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
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artikull shkencor
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artículo científico
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name
Autism spectrum disorders: the quest for genetic syndromes.
@en
type
label
Autism spectrum disorders: the quest for genetic syndromes.
@en
prefLabel
Autism spectrum disorders: the quest for genetic syndromes.
@en
P2093
P2860
P356
P1476
Autism spectrum disorders: the quest for genetic syndromes.
@en
P2093
Athina Ververi
Dimitrios I Zafeiriou
Efrosini Kalyva
Euthymia Vargiami
Vaios Dafoulis
P2860
P304
P356
10.1002/AJMG.B.32152
P577
2013-05-03T00:00:00Z