neurodevelopmental-disorder

Documents about neurodevelopmental-disorder

• Reading Remediation and Outcomes in Detention#804912ClinicalTrials.gov
• PURA-Related Neurodevelopmental Disorder: A Comprehensive Clinical Review of Genetics, Phenotype, and Emerging Therapeutic Strategies.#4433NCBI PubMed Central
• Biallelic WDR91 variants cause a neurodevelopmental disorder through impaired endosomal maturation and autophagy dysregulation#150421bioRxiv / medRxiv
• Mitigating multiple vulnerabilities experienced by learners diagnosed with Autism.#281861ResearchSpace
• A new neurodevelopmental disorder linked to heterozygous variants in UNC79#284355HAL (France)
• A recurrent CCDC82 frameshift variant associated with syndromic neurodevelopmental disorder in a consanguineous Pakistani family.#785700NCBI PubMed Central
• tES Modalities for the Treatment of ADHD#857972ClinicalTrials.gov
• Better Nights, Better Days for Children With Neurodevelopment Disorders#861437ClinicalTrials.gov
• Weighted Blankets for Sleep Disturbance Among Children With ADHD#886355ClinicalTrials.gov
• Biallelic WDR91 variants cause a neurodevelopmental disorder through impaired endosomal maturation and autophagy dysregulation#152059Unpaywall
• Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition#308276HAL (France)
• Selective vulnerability of excitatory cortical neurons to ZMYND11 loss reveals cell-type-specific mechanisms of neurodevelopmental disorder risk#379824bioRxiv / medRxiv
• 35 Individuals with HUWE1-Related Neurodevelopmental Disorder and Suggested Clinical Evaluations#200788ODU Digital Commons
• A comprehensive overview of the biological foundations of ADHD#273311Europe PMC
• Mechanisms of genetic variation underlying neurodevelopmental disorder phenotypes in the human cortex#651665eScholarship
• Auditory and Visual Noise as Possible Non-pharmacological Treatment of ADHD in School Children#877532ClinicalTrials.gov
• AIR-B4: Remaking Recess (RR)#894628ClinicalTrials.gov
• Magnetoencephalography in Children#905433ClinicalTrials.gov
• Bilingualism is Associated with Executive Function in Children With Autism Spectrum Disorder: A Systematic Review and Bayesian Meta-Analysis#176892OSF
• Ambulatory Polysomnography in Neurodiverse Children: Feasibility, Quality, and Satisfaction#838908ClinicalTrials.gov
• Pathogenic XPO1 variants cause a dominant neurodevelopmental disorder#250382HAL (France)
• SLC6A1-NDD Prospective Longitudinal Natural History Study#882711ClinicalTrials.gov
• Word Learning From Parentese in Autistic Children#914872ClinicalTrials.gov
• Monoallelic and biallelic KDM5A variants identified in patients with autism spectrum disorder#361778Europe PMC
• Biallelic protein truncating EXOSC6 variants cause a neurodevelopmental disorder with cerebellar atrophy, ataxia, and global developmental delay#619219bioRxiv / medRxiv
• Evaluation of Effectiveness of Child-oriented Goal-setting in Paediatric Rehabilitation (the ENGAGE Approach)#992874ClinicalTrials.gov
• Physiotherapy for Improving Mental Health in Children and Adolescents With ASD and ADHD#870760ClinicalTrials.gov
• De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder#31428HAL (France)
• De novo variants in NPTN cause a neurodevelopmental disorder with autism and neuroplastin-PMCA hypofunction#478573Europe PMC
• High Energy Formula Feeding in Infants With Congenital Heart Disease#849547ClinicalTrials.gov
• AIR-B4: Mind the Gap#917562ClinicalTrials.gov
• Novel SYNGAP1 Variant in an Adult Individual Affected by Intellectual Disability and Epilepsy: A Cold Case Solved through Whole-Exome Sequencing#274645IRIS
• ISGylation is disrupted by <i>UBA7</i> gene variants identified in individuals with neurodevelopmental disorder phenotypes#127521Europe PMC
• Digital-based Psychosocial Intervention for Parents of Children With Neurodevelopmental Disorders#874581ClinicalTrials.gov
• Genetic and Clinical Characterization of TANGO2 Deficiency Disorder: Insights from the Italian Multicentre Cohort#231317Europe PMC
• Online Evaluation of the Diagnostic Accuracy of BlinkLab's Digital Assessments for Autism#902424ClinicalTrials.gov
• Analysis of 14q12 microdeletions reveals novel regulatory loci for the neurodevelopmental disorder-related gene, <i>FOXG1</i>#145678Unpaywall
• Group B Streptococcus antibiotics treatment during pregnancy and the risk of four neurodevelopmental outcomes in Swedish children#273286Europe PMC
• Supplementary Material for: THUMPD1-Related Neurodevelopmental Disorder: A Novel Homozygous Loss-of-Function Variant with an Unusual Skeletal Phenotype: A Case Report#350262Figshare
• Bi-allelic variants in FSD1L cause a neurodevelopmental disorder overlapping with L1 syndrome#370717HAL (France)
• Genetic and Clinical Characterization of TANGO2 Deficiency Disorder: Insights from the Italian Multicentre Cohort#482824IRIS
• Neurobehavioural Development of Infants Born <30 Weeks Gestational Age Between Birth and Five Years of Age#854057ClinicalTrials.gov
• Can Psychopathy be Prevented? Clinical, Neuroimaging and Genetic Data#1010110ClinicalTrials.gov
• The Spectrum Between Us: An Analysis of The Lived Experiences of Selected Filipinos Aged 18-28 With a Sibling Diagnosed with Autism Spectrum Disorder#321313Animo Repository
• Variantes no gene EBF3 e variabilidade fenotípica do Transtorno do Espectro Autista#412929Repositório da UFES
• Clinical Efficacy of Cooperative Parent-Mediated Therapy (C-PMT_in_ASD)#895481ClinicalTrials.gov
• Pai.ACT: AI-Driven ACT Chatbot for Mental Health Triage and Service Evaluation#967837ClinicalTrials.gov
• A Quick and Reliable Eye Movement Test to Help Diagnose ADHD in Children.#1008446ClinicalTrials.gov
• A unified theory of restrictive and addictive eating: a life course model integrating generational transmission, neurodevelopmental risk, and ultra-processed food use disorder-a theoretical review.#262901NCBI PubMed Central
• Shared and disorder-specific prenatal and perinatal risk factors for neurodevelopmental disorders: a nationwide cohort study#431851Springer Nature OA