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本文引用的文献

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On the role of the reticular formation in vocal pattern generation.论网状结构在发声模式生成中的作用。
Behav Brain Res. 2007 Sep 4;182(2):308-14. doi: 10.1016/j.bbr.2006.11.027. Epub 2006 Dec 14.
2
Alterations in CNS activity induced by botulinum toxin treatment in spasmodic dysphonia: an H215O PET study.肉毒杆菌毒素治疗痉挛性发音障碍引起的中枢神经系统活动改变:一项H215O正电子发射断层扫描研究
J Speech Lang Hear Res. 2006 Oct;49(5):1127-46. doi: 10.1044/1092-4388(2006/081).
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Deep brain stimulation: postoperative issues.深部脑刺激:术后问题
Mov Disord. 2006 Jun;21 Suppl 14:S219-37. doi: 10.1002/mds.20957.
4
Long-term follow-up results of selective laryngeal adductor denervation-reinnervation surgery for adductor spasmodic dysphonia.内收型痉挛性发声障碍选择性喉内收肌去神经再支配手术的长期随访结果
Laryngoscope. 2006 Apr;116(4):635-42. doi: 10.1097/01.MLG.0000201990.97955.E4.
5
Task-specific hand dystonia: can too much plasticity be bad for you?特定任务性手部肌张力障碍:可塑性过强会对你有害吗?
Trends Neurosci. 2006 Apr;29(4):192-9. doi: 10.1016/j.tins.2006.02.007. Epub 2006 Mar 7.
6
Treatment of adductor-type spasmodic dysphonia by surgical myectomy: a preliminary report.手术切除肌肉治疗内收型痉挛性发音障碍:初步报告
Ann Otol Rhinol Laryngol. 2006 Feb;115(2):97-102. doi: 10.1177/000348940611500203.
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Localization of a vocal pattern generator in the pontine brainstem of the squirrel monkey.松鼠猴脑桥脑干中发声模式发生器的定位
Eur J Neurosci. 2006 Feb;23(3):840-4. doi: 10.1111/j.1460-9568.2006.04595.x.
8
"Silent event-related" fMRI reveals reduced sensorimotor activation in laryngeal dystonia.“静息事件相关”功能磁共振成像显示喉肌张力障碍患者感觉运动激活减少。
Neurology. 2005 Nov 22;65(10):1562-9. doi: 10.1212/01.wnl.0000184478.59063.db.
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Birdbrains could teach basal ganglia research a new song.笨鸟或许能给基底神经节研究带来新启发。
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Suppression of thyroarytenoid muscle responses during repeated air pressure stimulation of the laryngeal mucosa in awake humans.清醒人类喉黏膜反复气压刺激期间甲杓肌反应的抑制
Ann Otol Rhinol Laryngol. 2005 Apr;114(4):264-70. doi: 10.1177/000348940511400403.

痉挛性发声障碍的研究重点

Research priorities in spasmodic dysphonia.

作者信息

Ludlow Christy L, Adler Charles H, Berke Gerald S, Bielamowicz Steven A, Blitzer Andrew, Bressman Susan B, Hallett Mark, Jinnah H A, Juergens Uwe, Martin Sandra B, Perlmutter Joel S, Sapienza Christine, Singleton Andrew, Tanner Caroline M, Woodson Gayle E

机构信息

Laryngeal and Speech Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, 10 Center Drive, Bethesda, MD 20892, USA.

出版信息

Otolaryngol Head Neck Surg. 2008 Oct;139(4):495-505. doi: 10.1016/j.otohns.2008.05.624.

DOI:10.1016/j.otohns.2008.05.624
PMID:18922334
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2643054/
Abstract

OBJECTIVE

To identify research priorities to increase understanding of the pathogenesis, diagnosis, and improved treatment of spasmodic dysphonia.

STUDY DESIGN AND SETTING

A multidisciplinary working group was formed that included both scientists and clinicians from multiple disciplines (otolaryngology, neurology, speech pathology, genetics, and neuroscience) to review currently available information on spasmodic dysphonia and to identify research priorities.

RESULTS

Operational definitions for spasmodic dysphonia at different levels of certainty were recommended for diagnosis and recommendations made for a multicenter multidisciplinary validation study.

CONCLUSIONS

The highest priority is to characterize the disorder and identify risk factors that may contribute to its onset. Future research should compare and contrast spasmodic dysphonia with other forms of focal dystonia. Development of animal models is recommended to explore hypotheses related to pathogenesis. Improved understanding of the pathophysiology of spasmodic dysphonia should provide the basis for developing new treatment options and exploratory clinical trials.

SIGNIFICANCE

This document should foster future research to improve the care of patients with this chronic debilitating voice and speech disorder by otolaryngology, neurology, and speech pathology.

摘要

目的

确定研究重点,以增进对痉挛性发声障碍的发病机制、诊断及改善治疗的理解。

研究设计与背景

组建了一个多学科工作小组,成员包括来自多个学科(耳鼻喉科、神经科、言语病理学、遗传学和神经科学)的科学家和临床医生,以回顾目前关于痉挛性发声障碍的可用信息,并确定研究重点。

结果

推荐了不同确定性水平下痉挛性发声障碍的操作定义用于诊断,并为一项多中心多学科验证研究提出了建议。

结论

最优先的是对该疾病进行特征描述,并确定可能导致其发病的危险因素。未来的研究应将痉挛性发声障碍与其他形式的局灶性肌张力障碍进行比较和对比。建议开发动物模型以探索与发病机制相关的假说。对痉挛性发声障碍病理生理学的更好理解应为开发新的治疗方案和探索性临床试验提供基础。

意义

本文档应促进未来的研究,以改善耳鼻喉科、神经科和言语病理学对患有这种慢性致残性嗓音和言语障碍患者的治疗。