Reduced Cortical Complexity in Children with Prader-Willi Syndrome and Its Association with Cognitive Impairment and Developmental Delay
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference62 articles.
1. Deletions of Chromosome 15 as a Cause of the Prader-Willi Syndrome;DH Ledbetter;New England Journal of Medicine,1981
2. Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome;RD Nicholls;Nature,1989
3. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15;K Buiting;Nat Genet,1995
4. Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15;SB Cassidy;American Journal of Medical Genetics,1997
5. Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndrome;A Vogels;J Med Genet,2003
Cited by 32 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. Neuromodulation for the treatment of Prader-Willi syndrome – A systematic review;Neurotherapeutics;2024-04
2. Early psychomotor development and growth hormone therapy in children with Prader-Willi syndrome: a review;European Journal of Pediatrics;2023-11-21
3. A narrative review of the mechanisms and consequences of intermittent hypoxia and the role of advanced analytic techniques in pediatric autonomic disorders;Clinical Autonomic Research;2023-06
4. Progress in Brain Magnetic Resonance Imaging of Individuals with Prader–Willi Syndrome;Journal of Clinical Medicine;2023-01-29
5. The Brain in Prader-Willi Syndrome;Eating Disorders;2023
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3