Medico-legal investigation in an explicable case of congenital central hypoventilation syndrome due to a rare variant of the PHOX2B gene-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Medico-legal investigation in an explicable case of congenital central hypoventilation syndrome due to a rare variant of the PHOX2B gene

Published:2018-08 Issue: Volume:58 Page:1-5
ISSN:1752-928X
Container-title:Journal of Forensic and Legal Medicine
language:en
Short-container-title:Journal of Forensic and Legal Medicine

Author:

Ventura Francesco,Barranco Rosario,Bachetti Tiziana,Nozza Paolo,Fulcheri Ezio,Palmieri Antonella,Ceccherini Isabella

Publisher

Elsevier BV

Subject

Law,General Medicine,Pathology and Forensic Medicine

Reference29 articles.

1. Congenital central hypoventilation syndrome with PHOX2B gene mutation: are we missing the diagnosis?;Nirupam;Indian J Pediatr,2013

2. Congenital central hypoventilation syndrome;Weese-Mayer,2004

3. Congenital central hypoventilation syndrome and sudden infant death syndrome: disorders of autonomic regulation;Rand;Semin Pediatr Neurol,2013

4. The French congenital central hypoventilation syndrome registry: general data, phenotype, and genotype;Trang;Chest,2005

5. Unnatural causes of sudden unexpected deaths initially thought to be sudden infant death syndrome;Bajanowski;Int J Legal Med,2005

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. Post-mortem genetic analysis of sudden unexplained death in a young cohort: a whole-exome sequencing study;International Journal of Legal Medicine;2023-08-25

2. Non-polyalanine repeat mutation in PHOX2B is detected in autopsy cases of sudden unexpected infant death;PLOS ONE;2022-04-29

3. Evaluation of the effects of noninvasive ventilation on blood gas and depression levels of patients with obesity hypoventilation syndrome;Advanced Biomedical Research;2022

4. Multidisciplinary study of sudden unexpected infant death in Liguria (Italy): a nine-year report;Minerva Pediatrics;2021-11

5. Comprehensive Analysis of Genes Associated With Sudden Infant Death Syndrome;Frontiers in Pediatrics;2021-10-15

同舟云学术

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