• 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

Clinical practice guidelines for glycogen storage disease V & VII (McArdle disease and Tarui disease) from an international study group.

作者信息

Lucia Alejandro, Martinuzzi Andrea, Nogales-Gadea Gisela, Quinlivan Ros, Reason Stacey

机构信息

Faculty of Sports Sciences, Universidad Europea de Madrid, Spain; Centro de Investigación Biomédica en Red en Fragilidad y Envejecimiento Saludable (CIBERFES) and Research Institute of the Hospital 12 de Octubre ('imas12', PaHerg group), Madrid, Spain.

Conegliano Research Centre, IRCCS Eugenio Medea, Italy.

出版信息

Neuromuscul Disord. 2021 Dec;31(12):1296-1310. doi: 10.1016/j.nmd.2021.10.006. Epub 2021 Oct 28.

DOI:10.1016/j.nmd.2021.10.006
PMID:34848128
Abstract
摘要

相似文献

1
Clinical practice guidelines for glycogen storage disease V & VII (McArdle disease and Tarui disease) from an international study group.国际研究小组关于糖原贮积病V型和VII型（麦克尔迪病和塔瑞氏病）的临床实践指南。
Neuromuscul Disord. 2021 Dec;31(12):1296-1310. doi: 10.1016/j.nmd.2021.10.006. Epub 2021 Oct 28.
2
Unique Exercise Lactate Profile in Muscle Phosphofructokinase Deficiency (Tarui Disease); Difference Compared with McArdle Disease.肌肉磷酸果糖激酶缺乏症（Tarui病）独特的运动乳酸谱；与McArdle病的差异。
Front Neurol. 2016 May 30;7:82. doi: 10.3389/fneur.2016.00082. eCollection 2016.
3
Erratum to ``Clinical practice guidelines for glycogen storage disease V & VII (McArdle disease and Tarui disease) from an international study group'' [Neuromuscular Disorders 31 (2021) 1296-1310].《国际研究小组关于糖原贮积病V型和VII型（麦克尔迪病和塔瑞氏病）的临床实践指南》勘误 [《神经肌肉疾病》31卷（2021年）第1296 - 1310页] 。
Neuromuscul Disord. 2022 Feb;32(2):e3. doi: 10.1016/j.nmd.2022.01.004. Epub 2022 Feb 6.
4
A comparative study on glucagon effect between McArdle disease and Tarui disease.
Muscle Nerve. 1984 Sep;7(7):552-9. doi: 10.1002/mus.880070706.
5
Differential glucose metabolism in mice and humans affected by McArdle disease.受麦克尔迪氏病影响的小鼠和人类的葡萄糖代谢差异
Am J Physiol Regul Integr Comp Physiol. 2016 Aug 1;311(2):R307-14. doi: 10.1152/ajpregu.00489.2015. Epub 2016 Jun 8.
6
PYGM expression analysis in white blood cells: a complementary tool for diagnosing McArdle disease?白细胞中PYGM表达分析：诊断麦卡德尔病的辅助工具？
Neuromuscul Disord. 2014 Dec;24(12):1079-86. doi: 10.1016/j.nmd.2014.08.002. Epub 2014 Aug 21.
7
[Molecular pathology and gene diagnosis of muscle glycogenosis].
Nihon Rinsho. 1997 Dec;55(12):3302-6.
8
Differential Muscle Involvement in Mice and Humans Affected by McArdle Disease.麦克尔迪氏病对小鼠和人类肌肉的不同影响
J Neuropathol Exp Neurol. 2016 May;75(5):441-54. doi: 10.1093/jnen/nlw018. Epub 2016 Mar 30.
9
Exercising with blocked muscle glycogenolysis: Adaptation in the McArdle mouse.在肌肉糖原分解受阻的情况下进行运动：McArdle 小鼠的适应。
Mol Genet Metab. 2018 Jan;123(1):21-27. doi: 10.1016/j.ymgme.2017.11.006. Epub 2017 Nov 21.
10
Spontaneous "second wind" and glucose-induced second "second wind" in McArdle disease: oxidative mechanisms.麦克尔迪氏病中的自发“第二次呼吸”及葡萄糖诱导的第二次“第二次呼吸”：氧化机制
Arch Neurol. 2002 Sep;59(9):1395-402. doi: 10.1001/archneur.59.9.1395.

引用本文的文献

1
Cardiovascular involvement in glycogen storage diseases.糖原贮积病的心血管受累情况。
Nat Rev Cardiol. 2025 Jun 5. doi: 10.1038/s41569-025-01171-w.
2
Acute kidney injury after swimming: a pediatric case of McArdle disease.游泳后急性肾损伤：一例小儿麦克尔迪氏病病例
Pediatr Nephrol. 2025 Sep;40(9):2819-2822. doi: 10.1007/s00467-025-06758-6. Epub 2025 Apr 3.
3
Camptocormia as a feature of Mc Ardle's disease: A case report.凸轮状脊柱后凸作为麦卡德尔病的一个特征：一例报告。
Mol Genet Metab Rep. 2025 Feb 1;42:101197. doi: 10.1016/j.ymgmr.2025.101197. eCollection 2025 Mar.
4
McArdle Disease: A Diagnostic Challenge Due to Nonspecific Clinical Manifestations.麦克尔迪氏病：因临床表现不具特异性而带来的诊断难题。
Cureus. 2024 Dec 19;16(12):e76010. doi: 10.7759/cureus.76010. eCollection 2024 Dec.
5
Reporting a Novel Gene Mutation in Glycogen Storage Disease Type VII (Tarui Disease).糖原贮积病VII型（Tarui病）一种新基因突变的报告。
Ann Indian Acad Neurol. 2025 Jan 1;28(1):128-131. doi: 10.4103/aian.aian_574_24. Epub 2024 Nov 13.
6
Aerobic capacity and muscle proteome: Insights from a mouse model.有氧能力与肌肉蛋白质组：来自小鼠模型的见解
Exp Physiol. 2025 Feb;110(2):293-306. doi: 10.1113/EP092308. Epub 2024 Nov 21.
7
Carbohydrate Ingestion before Exercise for Individuals with McArdle Disease: Survey Evidence of Implementation and Perception in Real-World Settings.运动前碳水化合物摄入对 McArdle 病患者的影响：真实环境下实施和认知的调查证据。
Nutrients. 2024 May 9;16(10):1423. doi: 10.3390/nu16101423.
8
Measurement properties of the EQ-5D-3L, EQ-5D-5L, and SF-6Dv2 in patients with late-onset Pompe disease.迟发性庞贝病患者的 EQ-5D-3L、EQ-5D-5L 和 SF-6Dv2 的测量特性。
Eur J Health Econ. 2024 Dec;25(9):1505-1515. doi: 10.1007/s10198-024-01682-2. Epub 2024 Mar 12.
9
Toward an Understanding of GSD5 (McArdle disease): How Do Individuals Learn to Live with the Metabolic Defect in Daily Life.迈向 GSD5（麦卡德尔病）理解之路：个体如何学会在日常生活中应对代谢缺陷。
J Neuromuscul Dis. 2024;11(1):103-116. doi: 10.3233/JND-230027.
10
Diagnostic accuracy and the first genotype-phenotype correlation in glycogen storage disease type V.糖原贮积病 V 型的诊断准确性和首个基因型-表型相关性。
Pediatr Res. 2024 Jul;96(2):365-371. doi: 10.1038/s41390-023-02943-1. Epub 2023 Dec 5.