Neurodevelopmental Disorders Concept

subject area of

• (Unpacking) father involvement in the context of childhood neurodisability research: a scoping review  Academic Article
• A pathogenic UFSP2 variant in an autosomal recessive form of pediatric neurodevelopmental anomalies and epilepsy  Academic Article
• About my Child: measuring ‘Complexity’ in neurodisability. Evidence of reliability and validity  Academic Article
• Altered TAOK2 activity causes autism-related neurodevelopmental and cognitive abnormalities through RhoA signaling  Academic Article
• Characterization of Post-Thrombotic Syndrome in Children with Cardiac Disease  Academic Article
• Chorioamnionitis and risk of long-term neurodevelopmental disorders in offspring: a population-based cohort study  Academic Article
• Chronicity of mental comorbidity in children with new‐onset physical illness  Academic Article
• De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features  Academic Article
• Definitions and Operationalization of Mental Health Problems, Wellbeing and Participation Constructs in Children with NDD: Distinctions and Clarifications  Academic Article
• Diagnosis and clinical presentation of two individuals with a rareTCF20pathogenic variant  Academic Article
• Early detection and intervention for obsessive-compulsive disorder in childhood and adolescence  Academic Article
• Emerging proteomic approaches to identify the underlying pathophysiology of neurodevelopmental and neurodegenerative disorders  Academic Article
• 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
• 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
• Extensive cardiopulmonary resuscitation of preterm neonates at birth and mortality and developmental outcomes  Academic Article
• Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes  Academic Article
• Gestational and Lactational Exposure to an Environmentally-Relevant Mixture of Brominated Flame Retardants: Effects on Neurodevelopment and Metabolism  Academic Article
• Implications of Disability Severity on 24-Hour Movement Guideline Adherence Among Children With Neurodevelopmental Disorders in the United States  Academic Article
• Infantile-Onset Syndromic Cerebellar Ataxia and CACNA1G Mutations  Academic Article
• Long-term hearing and neurodevelopmental outcomes following Kawasaki disease: A population-based cohort study  Academic Article
• Loss of skills and onset patterns in neurodevelopmental disorders: Understanding the neurobiological mechanisms  Academic Article
• Maternal smoking and neurodevelopmental outcomes in infants <29 weeks gestation: a multicenter cohort study  Academic Article
• Mental, behavioral and neurodevelopmental disorders in the ICD-11: an international perspective on key changes and controversies  Academic Article
• Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression  Academic Article
• Mutations in EBF3 Disturb Transcriptional Profiles and Cause Intellectual Disability, Ataxia, and Facial Dysmorphism  Academic Article
• Neurodevelopment in 3–4 year old children exposed to maternal hyperglycemia or adiposity in utero  Academic Article
• Neurodevelopmental Outcomes of Infants at <29 Weeks of Gestation Born in Canada Between 2009 and 2016  Academic Article
• Neurodevelopmental and associated changes in a patient with Xp22.31 duplication  Academic Article
• Neurodevelopmental copy-number variants: A roadmap to improving outcomes by uniting patient advocates, researchers, and clinicians for collective impact  Academic Article
• Neurodevelopmental differences to social exclusion: An event-related neural oscillation study of children, adolescents, and adults.  Academic Article
• Neurodevelopmental outcomes of preterm infants conceived by assisted reproductive technology  Conference Paper
• OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome  Academic Article
• Oxytocin Receptor Polymorphisms are Differentially Associated with Social Abilities across Neurodevelopmental Disorders  Academic Article
• Paediatric targeted temperature management post cardiac arrest: A systematic review and meta-analysis  Academic Article
• Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome  Academic Article
• Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies  Academic Article
• Predictors of Long-Term Neurodevelopmental Outcome of Hypoxic-Ischemic Encephalopathy Treated with Therapeutic Hypothermia  Academic Article
• Pubertal stage, sex and behaviour in neurodevelopmental disorders versus typical development: a cross-sectional study  Academic Article
• Rhythm and timing as vulnerabilities in neurodevelopmental disorders  Academic Article
• SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females  Academic Article
• Screen Use and Mental Health Symptoms in Canadian Children and Youth During the COVID-19 Pandemic  Academic Article
• Severe Neurodevelopmental Impairment in Neonates Born Preterm: Impact of Varying Definitions in a Canadian Cohort  Academic Article
• Sleep Outcomes for Parents of Children With Neurodevelopmental Disabilities: A Systematic Review  Academic Article
• Supporting Children With Neurodevelopmental Disorders During the COVID-19 Pandemic  Academic Article
• The Need for a Developmentally Based Measure of Social Communication Skills  Academic Article
• Twin Birth Study: 2-year neurodevelopmental follow-up of the randomized trial of planned cesarean or planned vaginal delivery for twin pregnancy  Academic Article
• Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia  Academic Article
• Weight Status in the First 2 Years of Life and Neurodevelopmental Impairment in Extremely Low Gestational Age Newborns  Academic Article