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表型分析、病因因素与生物标志物:迈向自闭症谱系障碍的精准医学

Phenotyping, Etiological Factors, and Biomarkers: Toward Precision Medicine in Autism Spectrum Disorders.

作者信息

Beversdorf David Q

机构信息

Departments of Radiology, Neurology, and Psychological Sciences, and the Thompson Center for Autism and Neurodevelopmental Disorders, and William and Nancy Thompson Endowed Chair in Radiology, University of Missouri, Columbia, MO.

出版信息

J Dev Behav Pediatr. 2016 Oct;37(8):659-73. doi: 10.1097/DBP.0000000000000351.

Abstract

Despite the progress made in understanding the biology of autism spectrum disorder (ASD), effective biological interventions for the core symptoms remain elusive. Because of the etiological heterogeneity of ASD, identification of a "one-size-fits-all" treatment approach will likely continue to be challenging. A meeting was convened at the University of Missouri and the Thompson Center to discuss strategies for stratifying patients with ASD for the purpose of moving toward precision medicine. The "white paper" presented here articulates the challenges involved and provides suggestions for future solutions.

摘要

尽管在理解自闭症谱系障碍(ASD)生物学方面取得了进展,但针对核心症状的有效生物学干预措施仍然难以捉摸。由于ASD病因的异质性,确定一种“一刀切”的治疗方法可能仍然具有挑战性。在密苏里大学和汤普森中心召开了一次会议,讨论对ASD患者进行分层的策略,以朝着精准医学的方向发展。本文提出的“白皮书”阐述了其中涉及的挑战,并为未来的解决方案提供了建议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74b/5102276/2c32193b2951/jdbp-37-659-g001.jpg

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