• 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

Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0.

作者信息

Maeda Kenichi, Chong Pin Fee, Yamashita Fumiya, Akamine Satoshi, Kawakami Saori, Saito Kayoko, Takahata Yasushi, Kira Ryutaro

机构信息

Department of Pediatric Neurology, Fukuoka Children's Hospital, Fukuoka.

Institute of Medical Genetics, Tokyo Women's Medical University, Tokyo.

出版信息

Ann Neurol. 2019 Nov;86(5):801-802. doi: 10.1002/ana.25596. Epub 2019 Oct 3.

DOI:10.1002/ana.25596
PMID:31502271
Abstract
摘要

相似文献

1
Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0.0型脊髓性肌萎缩症中的全球中枢神经系统萎缩
Ann Neurol. 2019 Nov;86(5):801-802. doi: 10.1002/ana.25596. Epub 2019 Oct 3.
2
Reply to "Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0".对《脊髓性肌萎缩0型中的全球中枢神经系统萎缩》的回复
Ann Neurol. 2019 Nov;86(5):803. doi: 10.1002/ana.25597. Epub 2019 Oct 3.
3
Dystonic amyotrophy; dystonia and muscular atrophy.肌张力障碍性肌萎缩;肌张力障碍与肌肉萎缩。
Neurology. 1956 Feb;6(2):108-14. doi: 10.1212/wnl.6.2.108.
4
Autosomal dominant congenital spinal muscular atrophy: a true form of spinal muscular atrophy caused by early loss of anterior horn cells.常染色体显性先天性脊髓性肌萎缩症:一种由前角细胞早期丢失引起的真正的脊髓性肌萎缩症形式。
Brain. 2012 Jun;135(Pt 6):1714-23. doi: 10.1093/brain/aws108.
5
[Systemic diseases of the motor neurons. Amyotrophic lateral sclerosis, spinal progressive muscular atrophy, progressive bulbar paralysis, spastic spinal paralysis, peripheral nerve muscular atrophy].[运动神经元的全身性疾病。肌萎缩侧索硬化症、脊髓性进行性肌萎缩、进行性延髓麻痹、痉挛性脊髓麻痹、周围神经肌肉萎缩]
Naika. 1962 Dec;10:1067-9.
6
Distal infantile spinal muscular atrophy associated with paralysis of the diaphragm: a variant of infantile spinal muscular atrophy.伴有膈肌麻痹的远端型婴儿脊髓性肌萎缩症:婴儿脊髓性肌萎缩症的一种变异型
Am J Med Genet. 1989 Jul;33(3):328-35. doi: 10.1002/ajmg.1320330309.
7
Oxidative stress and disturbed glutamate transport in spinal muscular atrophy.脊髓性肌萎缩症中的氧化应激与谷氨酸转运紊乱
Brain Dev. 2002 Dec;24(8):770-5. doi: 10.1016/s0387-7604(02)00103-1.
8
Spinal muscular atrophy with respiratory distress type 1 (SMARD1).1型伴有呼吸窘迫的脊髓性肌萎缩症(SMARD1)
J Child Neurol. 2008 Feb;23(2):199-204. doi: 10.1177/0883073807310989.
9
[On the problem of spinal muscular atrophy resembling progressive muscular dystrophy (Kugelberg-Welander's juvenile muscular atrophy)].[关于脊髓性肌萎缩症类似进行性肌营养不良症(库格尔贝格 - 韦兰德少年型肌萎缩症)的问题]
Neurol Neurochir Psychiatr Pol. 1962 Sep-Oct;12:669-73.
10
Deletion and conversion in spinal muscular atrophy patients: is there a relationship to severity?脊髓性肌萎缩症患者的缺失和转换:与严重程度有关系吗?
Ann Neurol. 1997 Feb;41(2):230-7. doi: 10.1002/ana.410410214.

引用本文的文献

1
Neurodevelopmental and mental disorders in children with type I and presymptomatic spinal muscular atrophy.I型和症状前脊髓性肌萎缩症患儿的神经发育和精神障碍
Sci Rep. 2025 Jul 24;15(1):26984. doi: 10.1038/s41598-025-12484-8.
2
Neonatal spinal muscular atrophy with brain magnetic resonance imaging hypersignal: a case report.新生儿脊髓性肌萎缩伴脑磁共振成像高信号:一例报告
Front Pediatr. 2025 Apr 29;13:1508565. doi: 10.3389/fped.2025.1508565. eCollection 2025.
3
Network pharmacology approach to unravel the neuroprotective potential of natural products: a narrative review.
基于网络药理学方法解析天然产物的神经保护潜力:一篇综述
Mol Divers. 2025 Apr 25. doi: 10.1007/s11030-025-11198-3.
4
Quantitative synthetic MRI reveals grey matter abnormalities in patients with spinal muscular atrophy types 2 and 3.定量合成磁共振成像揭示2型和3型脊髓性肌萎缩症患者的灰质异常。
Quant Imaging Med Surg. 2025 Mar 3;15(3):2319-2328. doi: 10.21037/qims-24-1095. Epub 2025 Feb 26.
5
Reduced white matter integrity and disrupted brain network in children with type 2 and 3 spinal muscular atrophy.2型和3型脊髓性肌萎缩症患儿的白质完整性降低和脑网络中断。
J Neurodev Disord. 2025 Jan 24;17(1):3. doi: 10.1186/s11689-025-09592-x.
6
Macrostructural Brain Abnormalities in Spinal Muscular Atrophy: A Case-Control Study.脊髓性肌萎缩症患者大脑的宏观结构异常:一项病例对照研究。
Neurol Genet. 2024 Sep 20;10(5):e200193. doi: 10.1212/NXG.0000000000200193. eCollection 2024 Oct.
7
Cerebellar structural, astrocytic, and neuronal abnormalities in the SMNΔ7 mouse model of spinal muscular atrophy.脊髓性肌萎缩症 SMNΔ7 小鼠模型中的小脑结构、星形胶质细胞和神经元异常。
Brain Pathol. 2023 Sep;33(5):e13162. doi: 10.1111/bpa.13162. Epub 2023 May 22.
8
Brain Magnetic Resonance Imaging (MRI) in Spinal Muscular Atrophy: A Scoping Review.脑磁共振成像(MRI)在脊髓性肌萎缩症中的应用:一项范围综述。
J Neuromuscul Dis. 2023;10(4):493-503. doi: 10.3233/JND-221567.
9
Frontotemporal Pathology in Motor Neuron Disease Phenotypes: Insights From Neuroimaging.运动神经元病表型中的额颞叶病理学:神经影像学见解
Front Neurol. 2021 Aug 16;12:723450. doi: 10.3389/fneur.2021.723450. eCollection 2021.