Executive functioning and its relation to ASD and ADHD symptomatology in 22q11.2 deletion syndrome*-Reference-Cited by-同舟云学术

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Executive functioning and its relation to ASD and ADHD symptomatology in 22q11.2 deletion syndrome*

Published:2016-09-09 Issue:1 Volume:24 Page:1-19
ISSN:0929-7049
Container-title:Child Neuropsychology
language:en
Short-container-title:Child Neuropsychology

Author:

de Sonneville Leo M. J.¹²,Hidding Elske¹,van Engeland Herman³,Vorstman Jacob A. S.³,Sijmens-Morcus Monique E. J.¹,Swaab Hanna¹²

Affiliation:

1. Department of Clinical Child and Adolescent Studies, Leiden University, Leiden, The Netherlands

2. Leiden Institute for Brain and Cognition, Leiden, The Netherlands

3. Department of Psychiatry, Brain Center Rudolph Magnus, University Medical Centre Utrecht, Utrecht, The Netherlands

Publisher

Informa UK Limited

Subject

Developmental and Educational Psychology,Neuropsychology and Physiological Psychology,Pediatrics, Perinatology and Child Health

Link

https://tandfonline.com/doi/pdf/10.1080/09297049.2016.1221064

Reference66 articles.

1. Assessing executive functions in children: biological, psychological, and developmental considerations

2. Autistic Spectrum Disorders in Velo-cardio Facial Syndrome (22q11.2 Deletion)

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Neuropsychological Profile of 25 Brazilian Patients with 22q11.2 Deletion Syndrome: Effects of Clinical and Socioeconomic Variables;Genes;2024-05-08

2. Executive functioning in preschoolers with 22q11.2 deletion syndrome and the impact of congenital heart defects;Journal of Neurodevelopmental Disorders;2023-05-13

3. Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome;Genetics in Medicine;2023-03

4. Social behavior in 16p11.2 and 22q11.2 copy number variations: Insights from mice and humans;Genes, Brain and Behavior;2021-12-09

5. Learning from atypical development: A systematic review of executive functioning in children and adolescents with the 22q11.2 deletion syndrome;Developmental Review;2021-06

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