• 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
The Pathology of Paralysis with Muscular Degeneration (Paralysie Myosclerotique), or Paralysis with Apparent Hypertrophy.伴有肌肉变性的麻痹症（肌硬化性麻痹）或伴有假性肥大的麻痹症的病理学
Br Med J. 1867 Dec 14;2(363):541-2. doi: 10.1136/bmj.2.363.541.
2
The Pathology of Paralysis with Muscular Degeneration (Paralysie Myosclérotique).伴有肌肉变性的麻痹症病理学（肌硬化性麻痹症）
Chic Med Exam. 1868 Oct;9(10):614-617.
3
[Deux cas de paralysie périodique familiale].
Rev Neurol (Paris). 1954;91(5):347-52.
4
[Primitive myopathy in children; Association with the Leyden-Moebius type with pseudohypertrophic paralysis].
J Pediatr (Rio J). 1945 Apr;11:194.
5
Studies on pseudohypertrophic muscular paralysis or myosclerotic paralysis.
Arch Neurol. 1968 Dec;19(6):629-36. doi: 10.1001/archneur.1968.00480060099015.
6
[A CASE OF SPINAL PROGRESSIVE MUSCULAR ATROPHY (PROXIMAL TYPE)].[一例脊髓性进行性肌萎缩症（近端型）]
No To Shinkei. 1963 Oct;15:923-7.
7
[Localized muscular hypertrophy, tetanus syndrome, microcephaly and facial paralysis in a newborn baby].
Arch Fr Pediatr. 1949;6(6):656-60.
8
Pathological analysis of muscle hypertrophy and degeneration in muscular dystrophy in gamma-sarcoglycan-deficient mice.γ-肌聚糖缺乏小鼠肌肉营养不良中肌肉肥大和变性的病理分析
Neuromuscul Disord. 2003 Mar;13(3):193-206. doi: 10.1016/s0960-8966(02)00220-1.
9
[ON A POLYRADICULONEURITIC SYNDROME WITH PROGRESSIVE PARALYSIS IN 3 GENERATIONS OF A FAMILY].[关于一个家族三代人中患有进行性麻痹的多神经根神经炎综合征]
Arch Psychiatr Nervenkr. 1963 Dec 3;204:572-8. doi: 10.1007/BF00352711.
10
[Management of oculo-palpebral consequences in facial paralysis].[面瘫中眼睑相关后果的处理]
Ann Chir Plast Esthet. 2015 Oct;60(5):403-19. doi: 10.1016/j.anplas.2015.07.012. Epub 2015 Aug 28.

引用本文的文献

1
CircularRNA and Musculoskeletal Diseases.环状RNA与肌肉骨骼疾病
Adv Exp Med Biol. 2025;1485:437-448. doi: 10.1007/978-981-96-9428-0_25.
2
Advances in Dystrophinopathy Diagnosis and Therapy.肌营养不良症的诊断和治疗进展。
Biomolecules. 2023 Aug 28;13(9):1319. doi: 10.3390/biom13091319.
3
Chronic granulomatous disease associated with Duchenne muscular dystrophy caused by Xp21.1 contiguous gene deletion syndrome: Case report and literature review.由Xp21.1连续基因缺失综合征引起的与杜氏肌营养不良相关的慢性肉芽肿病：病例报告及文献复习
Front Genet. 2023 Jan 13;13:970204. doi: 10.3389/fgene.2022.970204. eCollection 2022.
4
Restoring Dystrophin Expression with Duchenne Muscular Dystrophy Exon 45 Skipping in Induced Pluripotent Stem Cell-Derived Cardiomyocytes.通过在诱导多能干细胞衍生的心肌细胞中跳过杜兴肌营养不良症外显子45来恢复抗肌萎缩蛋白表达
Methods Mol Biol. 2023;2587:141-151. doi: 10.1007/978-1-0716-2772-3_8.
5
Systemic delivery of an AAV9 exon-skipping vector significantly improves or prevents features of Duchenne muscular dystrophy in the Dup2 mouse.AAV9外显子跳跃载体的全身递送显著改善或预防了Dup2小鼠的杜氏肌营养不良症特征。
Mol Ther Methods Clin Dev. 2022 Jul 11;26:279-293. doi: 10.1016/j.omtm.2022.07.005. eCollection 2022 Sep 8.
6
Sphingosine Phosphate Lyase Is Upregulated in Duchenne Muscular Dystrophy, and Its Inhibition Early in Life Attenuates Inflammation and Dystrophy in Mdx Mice.鞘氨醇磷酸酶在杜氏肌营养不良症中上调，其在生命早期的抑制可减轻 mdx 小鼠的炎症和萎缩。
Int J Mol Sci. 2022 Jul 8;23(14):7579. doi: 10.3390/ijms23147579.
7
Restoring Protein Expression in Neuromuscular Conditions: A Review Assessing the Current State of Exon Skipping/Inclusion and Gene Therapies for Duchenne Muscular Dystrophy and Spinal Muscular Atrophy.恢复神经肌肉疾病中的蛋白质表达：评估外显子跳跃/包含和基因疗法治疗杜氏肌营养不良症和脊髓性肌萎缩症的现状的综述。
BioDrugs. 2021 Jul;35(4):389-399. doi: 10.1007/s40259-021-00486-7. Epub 2021 Jun 7.
8
Advances in Genetic Characterization and Genotype-Phenotype Correlation of Duchenne and Becker Muscular Dystrophy in the Personalized Medicine Era.个性化医疗时代杜兴氏和贝克氏肌肉营养不良症的基因特征及基因型-表型相关性研究进展
J Pers Med. 2020 Sep 3;10(3):111. doi: 10.3390/jpm10030111.
9
A well-tolerated core needle muscle biopsy process suitable for children and adults.一种耐受性良好的适用于儿童和成人的核心针肌肉活检方法。
Muscle Nerve. 2020 Dec;62(6):688-698. doi: 10.1002/mus.27041. Epub 2020 Sep 20.
10
Antisense oligonucleotides for the treatment of cardiomyopathy in Duchenne muscular dystrophy.用于治疗杜氏肌营养不良症心肌病的反义寡核苷酸。
Am J Transl Res. 2019 Mar 15;11(3):1202-1218. eCollection 2019.

The Pathology of Paralysis with Muscular Degeneration (Paralysie Myosclerotique), or Paralysis with Apparent Hypertrophy.

出版信息

Br Med J. 1867 Dec 14;2(363):541-2. doi: 10.1136/bmj.2.363.541.

DOI:10.1136/bmj.2.363.541
PMID:20744949
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2310746/
Abstract
摘要