Syndromic obesity with neurodevelopmental delay: Opportunities for targeted interventions
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference313 articles.
1. Diets and drugs for weight loss and health in obesity - an update;Aaseth;Biomed. Pharmacother.,2021
2. Mosaicism 45,X/46,X, t dic(Xp:Xp) in a girl with short stature;Abulhasan;Ann. Genet.,1990
3. First evidence of Smith-Magenis syndrome in mother and daughter due to a novel RAI mutation;Acquaviva;Am. J. Med. Genet.,2017
4. Observed dietary intake in adults with intellectual disability living in the community;Adolfsson;Food Nutr. Res.,2008
5. Expanding the clinical and molecular spectrum of PRMT7 mutations: 3 additional patients and review;Agolini;Clin. Genet.,2018
Cited by 4 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. A Comprehensive Review of Syndromic Forms of Obesity: Genetic Etiology, Clinical Features and Molecular Diagnosis;Current Obesity Reports;2024-01-26
2. Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalities;Genetics in Medicine;2023-01
3. Syndromic and Monogenic Obesity;Managing Pediatric Obesity Using Advanced Therapies;2023
4. Obesity and Overweight Among Children With Medical Complexity;Pediatrics;2022-12-27
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