نتایج جستجو برای: broad autism phenotype questionnaire bapq

تعداد نتایج: 527153  

Journal: :Functional neurology 2004
Paolo Brambilla Antonio Y Hardan Stefania Ucelli di Nemi Edgardo Caverzasi Jair C Soares Jorge Perez Francesco Barale

Autism is a neurodevelopmental syndrome characterized by impaired social and executive functions. Functional magnetic resonance imaging (fMRI) is a non-invasive technique that allows investigation of the neural networks underlying cognitive impairments in autism. In this article, brain imaging studies investigating the functional brain anatomy of autism are reviewed. Face recognition, theory of...

2011
Jennifer Gerdts Raphael Bernier

The presence of autism-related traits has been well documented in undiagnosed family members of individuals with autism spectrum disorder (ASD). The most common finding is mild impairments in social and communication skills that are similar to those shown by individuals with autism, but exhibited to a lesser degree. Termed the broader autism phenotype (BAP), these traits suggest a genetic liabi...

Journal: :Journal of autism and developmental disorders 2007
Sally Clifford Cheryl Dissanayake Quang M Bui Richard Huggins Annette K Taylor Danuta Z Loesch

The behavioural phenotype of autism was assessed in individuals with full mutation and premutation fragile X syndrome (FXS) using the Autism Diagnostic Observation Scale-Generic (ADOS-G) and the Autism Diagnostic Interview (ADI-R). The participants, aged 5-80 years, comprised 33 males and 31 females with full mutation, 7 males and 43 females with premutation, and 38 non-fragile X relatives (29 ...

Journal: :Neuron 2016
Steven A. Connor Ina Ammendrup-Johnsen Allen W. Chan Yasushi Kishimoto Chiaki Murayama Naokazu Kurihara Atsushi Tada Yuan Ge Hong Lu Ryan Yan Jeffrey M. LeDue Hirotaka Matsumoto Hiroshi Kiyonari Yutaka Kirino Fumio Matsuzaki Toshiharu Suzuki Timothy H. Murphy Yu Tian Wang Tohru Yamamoto Ann Marie Craig

Mutations in a synaptic organizing pathway contribute to autism. Autism-associated mutations in MDGA2 (MAM domain containing glycosylphosphatidylinositol anchor 2) are thought to reduce excitatory/inhibitory transmission. However, we show that mutation of Mdga2 elevates excitatory transmission, and that MDGA2 blocks neuroligin-1 interaction with neurexins and suppresses excitatory synapse devel...

Journal: :The European journal of neuroscience 2014
Stéphane J Baudouin

Autism is a developmental disorder characterised by a high heterogeneity of clinical diagnoses and genetic associations. This heterogeneity is a challenge for the identification of the pathophysiology of the disease and for the development of new therapeutic strategies. New conceptual approaches are being used to try to challenge this complexity and gene cluster analysis studies suggest that th...

Journal: :The international journal of neuropsychopharmacology 2010
Katsuaki Suzuki Katsuhiko Nishimura Genichi Sugihara Kazuhiko Nakamura Kenji J Tsuchiya Kaori Matsumoto Kiyokazu Takebayashi Haruo Isoda Harumi Sakahara Toshiro Sugiyama Masatsugu Tsujii Nori Takei Norio Mori

The aim of the present study was to investigate metabolite alterations in the hippocampal formation as they relate to aggression in high-functioning adults with autism. We measured concentrations of N-acetylaspartate (NAA), choline-containing compounds (Cho), and creatine plus phosphocreatine (Cr+PCr) in the hippocampal formation by proton magnetic resonance spectroscopy in 12 non-medicated mal...

Journal: :Autism research : official journal of the International Society for Autism Research 2017
Magdalena Glod Deborah M Riby Emma Honey Jacqui Rodgers

Sensory atypicalities are a common feature of autism spectrum disorder (ASD). To date, the relationship between sensory atypicalities in dyads of children with ASD and their parents has not been investigated. Exploring these relationships can contribute to an understanding of how phenotypic profiles may be inherited, and the extent to which familial factors might contribute towards children's s...

Journal: :American journal of mental retardation : AJMR 2008
Joanna F Moss Chris Oliver Katy Berg Gurmeash Kaur Lesley Jephcott Kim Cornish

Autism spectrum disorder characteristics have not been evaluated in Cornelia de Lange and Cri du Chat syndromes using robust assessments. The Autism Diagnostic Observation Schedule and Social Communication Questionnaire were administered to 34 participants with Cornelia de Lange syndrome and a comparison group of 23 participants with Cri du Chat syndrome (M ages 12.4 [SD = 3.8] and 10.3 years [...

2016
Guy L. McCormack Samuel Merritt Lisa Holsinger

Background: Children with autism have unusual sensory processing issues. The aim of this study was to examine how mothers comforted their children. Clinical observation has shown that mothers of children with autism often have difficulty calming their children. This study describes the differences in the response to comforting touch among children diagnosed with autism and normally developing c...

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