Neurodevelopmental Disorders
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subject area of
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(Unpacking) father involvement in the context of childhood neurodisability research: a scoping review Academic Article
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A pathogenic UFSP2 variant in an autosomal recessive form of pediatric neurodevelopmental anomalies and epilepsy Academic Article
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About my Child: measuring ‘Complexity’ in neurodisability. Evidence of reliability and validity Academic Article
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Altered TAOK2 activity causes autism-related neurodevelopmental and cognitive abnormalities through RhoA signaling Academic Article
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Characterization of Post-Thrombotic Syndrome in Children with Cardiac Disease Academic Article
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Chorioamnionitis and risk of long-term neurodevelopmental disorders in offspring: a population-based cohort study Academic Article
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Chronicity of mental comorbidity in children with new‐onset physical illness Academic Article
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De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features Academic Article
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Definitions and Operationalization of Mental Health Problems, Wellbeing and Participation Constructs in Children with NDD: Distinctions and Clarifications Academic Article
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Diagnosis and clinical presentation of two individuals with a rareTCF20pathogenic variant Academic Article
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Early detection and intervention for obsessive-compulsive disorder in childhood and adolescence Academic Article
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Emerging proteomic approaches to identify the underlying pathophysiology of neurodevelopmental and neurodegenerative disorders Academic Article
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Expanding the Phenotype: Neurodevelopmental Disorder, Mitochondrial, With Abnormal Movements and Lactic Acidosis, With or Without Seizures (NEMMLAS) Due to WARS2 Biallelic Variants, Encoding Mitochondrial Tryptophanyl-tRNA Synthase Academic Article
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Expanding the Phenotype: Neurodevelopmental Disorder, Mitochondrial, With Abnormal Movements and Lactic Acidosis, With or Without Seizures (NEMMLAS) due to WARS2 Biallelic Variants, Encoding Mitochondrial Tryptophanyl-tRNA Synthase Academic Article
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Extensive cardiopulmonary resuscitation of preterm neonates at birth and mortality and developmental outcomes Academic Article
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Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes Academic Article
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Gestational and Lactational Exposure to an Environmentally-Relevant Mixture of Brominated Flame Retardants: Effects on Neurodevelopment and Metabolism Academic Article
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Implications of Disability Severity on 24-Hour Movement Guideline Adherence Among Children With Neurodevelopmental Disorders in the United States Academic Article
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Infantile-Onset Syndromic Cerebellar Ataxia and CACNA1G Mutations Academic Article
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Long-term hearing and neurodevelopmental outcomes following Kawasaki disease: A population-based cohort study Academic Article
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Loss of skills and onset patterns in neurodevelopmental disorders: Understanding the neurobiological mechanisms Academic Article
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Maternal smoking and neurodevelopmental outcomes in infants <29 weeks gestation: a multicenter cohort study Academic Article
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Mental, behavioral and neurodevelopmental disorders in the ICD-11: an international perspective on key changes and controversies Academic Article
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Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression Academic Article
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Mutations in EBF3 Disturb Transcriptional Profiles and Cause Intellectual Disability, Ataxia, and Facial Dysmorphism Academic Article
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Neurodevelopment in 3–4 year old children exposed to maternal hyperglycemia or adiposity in utero Academic Article
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Neurodevelopmental Outcomes of Infants at <29 Weeks of Gestation Born in Canada Between 2009 and 2016 Academic Article
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Neurodevelopmental and associated changes in a patient with Xp22.31 duplication Academic Article
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Neurodevelopmental copy-number variants: A roadmap to improving outcomes by uniting patient advocates, researchers, and clinicians for collective impact Academic Article
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Neurodevelopmental differences to social exclusion: An event-related neural oscillation study of children, adolescents, and adults. Academic Article
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Neurodevelopmental outcomes of preterm infants conceived by assisted reproductive technology Conference Paper
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OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome Academic Article
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Oxytocin Receptor Polymorphisms are Differentially Associated with Social Abilities across Neurodevelopmental Disorders Academic Article
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Paediatric targeted temperature management post cardiac arrest: A systematic review and meta-analysis Academic Article
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Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome Academic Article
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Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies Academic Article
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Predictors of Long-Term Neurodevelopmental Outcome of Hypoxic-Ischemic Encephalopathy Treated with Therapeutic Hypothermia Academic Article
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Pubertal stage, sex and behaviour in neurodevelopmental disorders versus typical development: a cross-sectional study Academic Article
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Rhythm and timing as vulnerabilities in neurodevelopmental disorders Academic Article
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SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females Academic Article
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Screen Use and Mental Health Symptoms in Canadian Children and Youth During the COVID-19 Pandemic Academic Article
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Severe Neurodevelopmental Impairment in Neonates Born Preterm: Impact of Varying Definitions in a Canadian Cohort Academic Article
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Sleep Outcomes for Parents of Children With Neurodevelopmental Disabilities: A Systematic Review Academic Article
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Supporting Children With Neurodevelopmental Disorders During the COVID-19 Pandemic Academic Article
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The Need for a Developmentally Based Measure of Social Communication Skills Academic Article
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Twin Birth Study: 2-year neurodevelopmental follow-up of the randomized trial of planned cesarean or planned vaginal delivery for twin pregnancy Academic Article
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Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia Academic Article
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Weight Status in the First 2 Years of Life and Neurodevelopmental Impairment in Extremely Low Gestational Age Newborns Academic Article