Michael Isfort,David Lacomis
Michael Isfort
This update begins with a section on inflammatory myopathies covering inclusion body myositis in younger patients, the possibility of a pathogenic role for anti-cN1A antibodies, and a negative trial of arimoclomol in inclusion body myositis...
Diagnosing X-Linked Myopathy With Excessive Autophagy After 30 years: Genetic, Ultrasonographic, and Electrodiagnostic Findings [0.03%]
X-连锁自噬过多型肌病的诊断：遗传学、超声和电生理特征
Vanessa Dwairi,Alaina Giacobbe,Sasa Zivkovic et al.
Vanessa Dwairi et al.
X-linked myopathy with excessive autophagy is a rare disorder caused by a mutation in the vacuolar ATPase assembly factor gene which causes slowly progressive early onset proximal weakness and loss of ambulation by the age of 50-70 years. E...
Utility of the Repetitive Nerve Stimulation Test and Needle EMG in the Trapezius Muscle for the Early Diagnosis of ALS [0.03%]
重复神经刺激检查和斜方肌针电极检测在早期诊断ALS中的作用
Kazusa Takahashi,Yuichi Hamada,Masahito Kobayashi et al.
Kazusa Takahashi et al.
Objectives: To document the utility of decremental responses in the repetitive nerve stimulation test (RNS) and spontaneous activities in needle electromyography (EMG) in the trapezius muscle for the diagnosis of amyotrop...
Ali Sreij,Raja Sawaya
Ali Sreij
MuSK Antibody-Positive Myasthenia Gravis With SARS CoV-2 Infection: A Case Report and Literature Review [0.03%]
抗MuSK抗体阳性重症肌无力伴SARS-CoV-2感染的病例报告和文献复习
Shreyashi Jha,Santosh Kumar Pendyala
Shreyashi Jha
The Course of Double Seronegative Myasthenia During Pregnancy May Depend on Diagnostic Criteria and Study Design [0.03%]
妊娠期间重症肌无力的诊治依赖于诊断标准和研究设计的不同可能影响疾病进程
Josef Finsterer
Josef Finsterer
Evaluation of Neuromuscular Provider Perceptions and Office Setup for Evaluating Patients With Disabilities [0.03%]
神经肌肉提供者对残疾患者评估的感知和诊所设置的评估
Adeel S Zubair,John Paul Mikhaiel,Seth M Keller
Adeel S Zubair
Comparing Seropositive and Seronegative Myasthenia During Pregnancy Requires Appropriate Design and Diagnostic Testing [0.03%]
自身抗体阳性和阴性重症肌无力患者的妊娠比较需要合理的设计和诊断检测方法
Josef Finsterer
Josef Finsterer
Scleroderma-Polymyositis Overlap Syndrome as a Potential Bulbar Amyotrophic Lateral Sclerosis Mimic [0.03%]
硬皮病-多发性肌炎重叠综合征作为进行性延髓型肌肉萎缩症的潜在模仿病症
Alessandra Maccabeo,Emanuela Salustro,Mauro Sanna et al.
Alessandra Maccabeo et al.
Myopathy With Crescent of Nuclei: A Novel Histopathologic Finding in Desminopathy [0.03%]
肌病伴核新月形分布：Desmin肌病的新型组织病理学特征
Andre Granger,Eric J Sorenson,Duygu Selcen et al.
Andre Granger et al.