Characteristics of patients with sporadic inclusion body myositis.

NIAID Data Ecosystem2026-05-02 收录

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https://figshare.com/articles/dataset/Characteristics_of_patients_with_sporadic_inclusion_body_myositis_/26438936 数据链接链接失效反馈

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资源简介：

Characteristics of patients with sporadic inclusion body myositis.

创建时间：

2024-08-01

肌萎缩侧索硬化束颤分布研究和卒中后下运动神经元病变的电生理、超声和病理研究

神经肌肉疾病

超声诊断

目的：肌肉束颤作为早期诊断肌萎缩侧索硬化（amyotrophic lateral sclerosis，ALS）的重要提示，一直以来受到广泛关注。超声具有无创性，且检测束颤的敏感性高于针极肌电图，目前已成为观察束颤的重要辅助手段。本研究旨在探讨超声下ALS不同部位束颤的差异及其与临床因素之间的关系，以探索ALS的束颤分布规律。方法：我们纳入了113名ALS患者，收集其临床资料。在超声下检测患者球部

中国科学院中国科学技术大学科学数据中心280

The mechanism underlying transient weakness in myotonia congenita

神经肌肉疾病

离子通道病理学

In addition to the hallmark muscle stiffness, patients with recessive myotonia congenita (Becker disease) experience debilitating bouts of transient weakness that remain poorly understood despite year

NIAID Data Ecosystem50

The ER-Bound RING Finger Protein 5 (RNF5/RMA1) Causes Degenerative Myopathy in Transgenic Mice and Is Deregulated in Inclusion Body Myositis

包涵体肌炎

肌肉退化动物模型

Growing evidence supports the importance of ubiquitin ligases in the pathogenesis of muscular disorders, although underlying mechanisms remain largely elusive. Here we show that the expression of RNF5

NIAID Data Ecosystem30

Additional file 1 of Multi-omics analysis in inclusion body myositis identifies mir-16 responsible for HLA overexpression

包涵体肌炎

差异基因表达分析

Additional file 1: Differential gene expression. Table with results of differential gene expression analysis.

Figshare2025-01-16 更新70

Antioxidant-mediated protective role of Hericium erinaceus (Bull.: Fr.) Pers. against oxidative damage in fibroblasts from Friedreich’s ataxia patient

抗氧化作用

神经肌肉疾病

Abstract Friedreich’s ataxia (FRDA) is a progressive neuromuscular disorder caused by substantial decrease of mitochondrial protein frataxin responsible for biogenesis of iron-sulphur clusters and pro

DataCite Commons2020-08-26 更新50

Characteristics of patients with sporadic inclusion body myositis.

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