• 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

相似文献

1
Dysmorphic neuromuscular junctions associated with motor ability in cerebral palsy.
Muscle Nerve. 2005 Nov;32(5):626-32. doi: 10.1002/mus.20401.
2
Neuromuscular junctions in cerebral palsy: presence of extrajunctional acetylcholine receptors.
Anesthesiology. 2002 Feb;96(2):330-5. doi: 10.1097/00000542-200202000-00017.
3
Disruption of basal lamina components in neuromotor synapses of children with spastic quadriplegic cerebral palsy.痉挛性四肢瘫痪脑瘫患儿运动神经元突触基底膜成分的破坏。
PLoS One. 2013 Aug 16;8(8):e70288. doi: 10.1371/journal.pone.0070288. eCollection 2013.
4
Heterogeneity of neuromuscular junctions in striated muscle of human esophagus demonstrated by triple staining for the vesicular acetylcholine transporter, alpha-bungarotoxin, and acetylcholinesterase.通过对囊泡乙酰胆碱转运体、α-银环蛇毒素和乙酰胆碱酯酶进行三重染色,证明人食管横纹肌中神经肌肉接头的异质性。
Cell Tissue Res. 2006 May;324(2):181-8. doi: 10.1007/s00441-005-0154-4. Epub 2006 Jan 26.
5
Origin of acetylcholinesterase in the neuromuscular junction formed in the in vitro innervated human muscle.体外神经支配的人体肌肉中形成的神经肌肉接头处乙酰胆碱酯酶的起源。
Eur J Neurosci. 2004 Dec;20(11):2865-71. doi: 10.1111/j.1460-9568.2004.03752.x.
6
The relationship between gross motor function and participation restriction in children with cerebral palsy: an exploratory analysis.脑瘫患儿粗大运动功能与参与限制之间的关系:一项探索性分析。
Child Care Health Dev. 2007 Jan;33(1):22-7. doi: 10.1111/j.1365-2214.2006.00634.x.
7
C Histomorphology of neuromuscular junction in Duchenne muscular dystrophy.C 杜氏肌营养不良症中神经肌肉接头的组织形态学
Paediatr Anaesth. 2008 Mar;18(3):256-9. doi: 10.1111/j.1460-9592.2008.02411.x.
8
Expression and distribution of acetylcholinesterase among the cellular components of the neuromuscular junction formed in human myotube in vitro.乙酰胆碱酯酶在体外人肌管形成的神经肌肉接头细胞成分中的表达与分布。
Chem Biol Interact. 2005 Dec 15;157-158:29-35. doi: 10.1016/j.cbi.2005.10.003. Epub 2005 Oct 26.
9
Frequency and severity of visual sensory and motor deficits in children with cerebral palsy: gross motor function classification scale.脑瘫患儿视觉感觉和运动功能障碍的频率及严重程度:粗大运动功能分类量表
Invest Ophthalmol Vis Sci. 2008 Feb;49(2):572-80. doi: 10.1167/iovs.07-0525.
10
Butyrylcholinesterase and the control of synaptic responses in acetylcholinesterase knockout mice.丁酰胆碱酯酶与乙酰胆碱酯酶基因敲除小鼠突触反应的调控
Life Sci. 2007 May 30;80(24-25):2380-5. doi: 10.1016/j.lfs.2007.03.011. Epub 2007 Mar 28.

引用本文的文献

1
DNA Methylation Analysis Reveals Distinct Patterns in Satellite Cell-Derived Myogenic Progenitor Cells of Subjects with Spastic Cerebral Palsy.DNA甲基化分析揭示痉挛型脑瘫患者卫星细胞源性肌源性祖细胞中的独特模式。
J Pers Med. 2022 Nov 30;12(12):1978. doi: 10.3390/jpm12121978.
2
Resistance to Neuromuscular Blockade by Rocuronium in Surgical Patients with Spastic Cerebral Palsy.痉挛型脑瘫手术患者对罗库溴铵神经肌肉阻滞的抵抗作用
J Pers Med. 2021 Aug 3;11(8):765. doi: 10.3390/jpm11080765.
3
Temporal changes in the muscle extracellular matrix due to volumetric muscle loss injury.由于容积性肌肉损失损伤导致的肌肉细胞外基质的时间变化。
Connect Tissue Res. 2022 Mar;63(2):124-137. doi: 10.1080/03008207.2021.1886285. Epub 2021 Feb 15.
4
Diaphragm neuromuscular transmission failure in a mouse model of an early-onset neuromotor disorder.早期运动神经障碍小鼠模型中膈肌神经肌肉传递失败。
J Appl Physiol (1985). 2021 Mar 1;130(3):708-720. doi: 10.1152/japplphysiol.00864.2020. Epub 2020 Dec 31.
5
Contribution of extracellular matrix components to the stiffness of skeletal muscle contractures in patients with cerebral palsy.细胞外基质成分对脑瘫患者骨骼肌挛缩硬度的贡献。
Connect Tissue Res. 2021 May;62(3):287-298. doi: 10.1080/03008207.2019.1694011. Epub 2019 Nov 28.
6
Characterization of torque generating properties of ankle plantar flexor muscles in ambulant adults with cerebral palsy.偏瘫成年人踝关节跖屈肌产生扭矩特性的特征分析。
Eur J Appl Physiol. 2019 May;119(5):1127-1136. doi: 10.1007/s00421-019-04102-z. Epub 2019 Feb 18.
7
Neuromotor synapses in Escobar syndrome.Escobar 综合征的神经运动突触。
Am J Med Genet A. 2013 Dec;161A(12):3042-8. doi: 10.1002/ajmg.a.36154. Epub 2013 Aug 16.
8
Disruption of basal lamina components in neuromotor synapses of children with spastic quadriplegic cerebral palsy.痉挛性四肢瘫痪脑瘫患儿运动神经元突触基底膜成分的破坏。
PLoS One. 2013 Aug 16;8(8):e70288. doi: 10.1371/journal.pone.0070288. eCollection 2013.
9
A predictive mathematical model of muscle forces for children with cerebral palsy.一种针对脑瘫儿童肌肉力量的预测数学模型。
Dev Med Child Neurol. 2009 Dec;51(12):949-58. doi: 10.1111/j.1469-8749.2009.03350.x. Epub 2009 Aug 24.
10
Novel transcriptional profile in wrist muscles from cerebral palsy patients.脑瘫患者腕部肌肉中的新型转录谱。
BMC Med Genomics. 2009 Jul 14;2:44. doi: 10.1186/1755-8794-2-44.

Dysmorphic neuromuscular junctions associated with motor ability in cerebral palsy.

作者信息

Theroux Mary C, Oberman Karyn G, Lahaye Justine, Boyce Bobbie A, Duhadaway David, Miller Freeman, Akins Robert E

机构信息

Nemours Biomedical Research, AI duPont Hospital for Children, Wilmington, Delaware 19803, USA.

出版信息

Muscle Nerve. 2005 Nov;32(5):626-32. doi: 10.1002/mus.20401.

DOI:10.1002/mus.20401
PMID:16025530
Abstract

Cerebral palsy (CP) is the most prevalent neurologic disease in children and a leading cause of severe physical disability. Research and clinical experience indicate that children with CP have abnormal neuromuscular junctions (NMJs), and we present evidence that nonapposition of neuromuscular junction components is associated with the severity of motor system deficit in CP. Leg muscle biopsies collected from ambulatory (n = 21) or nonambulatory (n = 38) CP patients were stained in order to detect acetylcholine receptor (AChR) and acetylcholine esterase (AChE). Image analysis was used to calculate the extra-AChE spread (EAS) of AChR staining to estimate the amount of AChR occurring outside the functional, AChE-delimited NMJ. Nonambulatory children exhibited higher average EAS (P = 0.025) and had a greater proportion of their NMJs with significantly elevated EAS (P = 0.023) than ambulatory children. These results indicate that physical disability in children with CP is associated with structurally dysmorphic NMJs, which has important implications for the management of CP patients, especially during surgery and anesthesia.

摘要