• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Autonomic function in hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease).

作者信息

Ingall T J, McLeod J G

机构信息

Department of Medicine, University of Sydney, NSW, Australia.

出版信息

Muscle Nerve. 1991 Nov;14(11):1080-3. doi: 10.1002/mus.880141107.

DOI:10.1002/mus.880141107
PMID:1745281
Abstract

Autonomic tests of heart rate and blood pressure control using both invasive and noninvasive techniques were performed on 11 patients with hereditary motor and sensory neuropathy (HMSN) types 1, and 4 patients with HMSN type 2. The results were compared with those of 76 control subjects. No significant difference was found between the patient and control groups. Impairment of sweating on the extremities was found in patients with HMSN types 1 and 2, consistent with distal degeneration of sympathetic fibers in peripheral nerves, but there were no abnormalities of cardiovascular reflex control mechanisms.

摘要

相似文献

1
Autonomic function in hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease).
Muscle Nerve. 1991 Nov;14(11):1080-3. doi: 10.1002/mus.880141107.
2
Abnormal responses to cold stress in Charcot-Marie-Tooth I syndrome.夏科-马里-图斯I型综合征对冷应激的异常反应。
Arch Phys Med Rehabil. 1994 Jul;75(7):787-91.
3
Electrophysiological findings in hereditary motor and sensory neuropathy type I and II--a conduction velocity study.遗传性运动和感觉神经病I型和II型的电生理发现——一项传导速度研究。
Electromyogr Clin Neurophysiol. 1998 Mar;38(2):95-101.
4
Genetic linkage evidence for heterogeneity in Charcot-Marie-Tooth neuropathy (HMSN type I).夏科-马里-图思神经病变(遗传性运动感觉神经病I型)异质性的遗传连锁证据
Ann Neurol. 1983 Dec;14(6):679-84. doi: 10.1002/ana.410140612.
5
Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: a 20-year study.1B型遗传性运动感觉神经病原发病例家族的临床和病理表型:一项为期20年的研究
Ann Neurol. 1997 Apr;41(4):463-9. doi: 10.1002/ana.410410409.
6
Early detection of diabetic neuropathy: a neurophysiological study on 100 patients.糖尿病性神经病变的早期检测:对100例患者的神经生理学研究
Electromyogr Clin Neurophysiol. 1997 Oct;37(7):399-407.
7
Autonomic function in patients with hereditary motor and sensory neuropathy type I and Lambert-Eaton myasthenic syndrome.I型遗传性运动和感觉神经病及兰伯特-伊顿肌无力综合征患者的自主神经功能
Electromyogr Clin Neurophysiol. 1999 Sep;39(6):349-53.
8
The autonomic laboratory.自主神经实验室。
Am J Electroneurodiagnostic Technol. 1999 Jun;39(2):65-76.
9
Charcot-Marie-Tooth disease in northern Finland.
Ann Clin Res. 1986;18(3):154-9.
10
Somatic and autonomic function in progressive autonomic failure and multiple system atrophy.进行性自主神经功能衰竭和多系统萎缩中的躯体和自主神经功能
Ann Neurol. 1987 Dec;22(6):692-9. doi: 10.1002/ana.410220604.

引用本文的文献

1
Small nerve fiber involvement in CMT1A.CMT1A中的小神经纤维受累情况。
Neurology. 2015 Jan 27;84(4):407-14. doi: 10.1212/WNL.0000000000001188. Epub 2014 Dec 24.
2
Corneal confocal microscopy detects small-fiber neuropathy in Charcot-Marie-Tooth disease type 1A patients.角膜共聚焦显微镜可检测到 1A 型遗传性运动感觉神经病患者的小纤维神经病。
Muscle Nerve. 2012 Nov;46(5):698-704. doi: 10.1002/mus.23377. Epub 2012 Sep 19.