Search Results - "Guinchat, Vincent"
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Pre-, peri- and neonatal risk factors for autism
Published in Acta obstetricia et gynecologica Scandinavica (01-03-2012)“…To identify pre-, peri- and neonatal risk factors for pervasive developmental disorders (PDD). We searched the Medline database through March 2011 for relevant…”
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Editorial: Neurodevelopmental, neuropsychiatric and psychosocial correlates of joint hypermobility and related disorders
Published in Frontiers in psychiatry (12-12-2022)Get full text
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Autism, Joint Hypermobility-Related Disorders and Pain
Published in Frontiers in psychiatry (07-12-2018)“…Autism Spectrum Disorder (ASD) and Joint Hypermobility-Related Disorders are blanket terms for two etiologically and clinically heterogeneous groups of…”
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Case Report: Opioid Use Disorder Associated With Low/Moderate Dose of Loperamide in an Intellectual Disability Patient With CYP3A and P-Glycoprotein Reduced Activity
Published in Frontiers in psychiatry (23-06-2022)“…Loperamide is an over-the-counter antidiarrheal for which increasing cases of abuse or misuse are described. We report the onset of opioid use disorder…”
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Changes in the Use of Emergency Care for the Youth With Mental Health Problems Over Decades: A Repeated Cross Sectional Study
Published in Frontiers in psychiatry (2019)“…To understand whether changes exist in the types of youths mental health problems addressed in emergency in a context of increasing demand, we conducted a…”
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Compressive Garments in Individuals with Autism and Severe Proprioceptive Dysfunction: A Retrospective Exploratory Case Series
Published in Children (Basel) (01-07-2020)“…(1) Background: Compression garments (CGs) are an adjuvant treatment for generalized joint hypermobility (GJH), including the Ehlers–Danlos…”
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Management of Severe Developmental Regression in an Autistic Child with a 1q21.3 Microdeletion and Self-Injurious Blindness
Published in Case reports in psychiatry (01-01-2017)“…We report the case of a young boy with nonverbal autism and intellectual disability, with a rare de novo 1q21.3 microdeletion. The patient had early and…”
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Developmental Phenotype of the Rare Case of DJ Caused by a Unique ADNP Gene De Novo Mutation
Published in Journal of molecular neuroscience (01-07-2019)Get full text
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Very early signs of autism reported by parents include many concerns not specific to autism criteria
Published in Research in autism spectrum disorders (01-04-2012)“…► We analyzed 459 questionnaires completed by French parents to assess their first concerns of autism in their child. ► Very early signs of autism were not…”
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Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders
Published in PLoS genetics (01-02-2012)“…Autism spectrum disorders (ASD) are a heterogeneous group of neurodevelopmental disorders with a complex inheritance pattern. While many rare variants in…”
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Acute behavioral crises in psychiatric inpatients with autism spectrum disorder (ASD): Recognition of concomitant medical or non-ASD psychiatric conditions predicts enhanced improvement
Published in Research in developmental disabilities (01-03-2015)“…•Resistant acute situations associated with autism and/or ID can improve in inpatient neurobehavioral units with interdisciplinary collaboration.•Common…”
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Barriers Facing Direct Support Professionals When Supporting Older Adults Presenting with Intellectual Disabilities and Unusual Dementia-Related Behavior: A Multi-Site, Multi-Methods Study
Published in Disabilities (Basel, Switzerland) (01-12-2022)“…Introduction: Increased life expectancy among people with intellectual disabilities (ID) raises the risk of their diagnosis being superimposed by behavioral…”
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Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism
Published in Molecular psychiatry (01-07-2016)“…Autism spectrum disorder (ASD) is a common neurodevelopmental condition characterized by marked genetic heterogeneity. Recent studies of rare structural and…”
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Electroconvulsive therapy in adolescents with intellectual disability and severe self-injurious behavior and aggression: a retrospective study
Published in European child & adolescent psychiatry (2013)“…Efficacious intervention for severe, treatment-refractory self-injurious behavior and aggression (SIB/AGG) in children and adolescents with intellectual…”
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CNOT2 haploinsufficiency in a 40‐year‐old man with intellectual disability, autism, and seizures
Published in American journal of medical genetics. Part A (01-08-2021)Get full text
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School achievement of deaf children ten years after cochlear implantation
Published in Neuropsychiatrie de l'enfance et de l'adolescence (01-01-2019)“…This longitudinal study examines school achievement in terms of grade failures among deaf children ten years after cochlear implantation according to the…”
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Cornelia de Lange and Ehlers-Danlos: comorbidity of two rare syndromes
Published in BMJ case reports (01-02-2016)“…We present a case of a young adult with both Cornelia de Lange syndrome and Ehlers-Danlos syndrome. The patient showed non-verbal autism, intellectual…”
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Trends, perinatal characteristics, and medical conditions in pervasive developmental disorders
Published in Developmental medicine and child neurology (01-11-2006)“…Our aim was to study trends in the prevalence of pervasive developmental disorders (PDD) and to quantify their association with morphogenetic anomalies and…”
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Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism
Published in American journal of medical genetics. Part A (01-09-2010)“…We describe a patient with autism and a paracentric inversion of chromosome 2q14.2q37.3, with a concurrent duplication of the proximal breakpoint at…”
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