Neuromuscular Ultrasound Identification of Musculocutaneous Fasciculopathies in Neuralgic Amyotrophy [0.03%]
神经肌肉超声识别神经性肌萎缩的肌皮神经营养不良病灶
Michael D Zhitnitsky,Julia T Carter,Marco Rizzo et al.
Michael D Zhitnitsky et al.
Tofersen for Amyotrophic Lateral Sclerosis: Genetic Treatment With Precision Medicine: The Future of ALS Treatment [0.03%]
ALS的基因精准医疗：Tofersen治疗肌萎缩性侧索硬化症的未来
Abdullah Ashraf Hamad
Abdullah Ashraf Hamad
Oculopharyngeal Muscular Dystrophy Responding to Treatment: A Report of 2 Cases [0.03%]
对治疗有反应的双眼睑咽部肌营养不良症：2例报道
Ali Sreij,Ghaysaa El Hasan,Rawan Chakas et al.
Ali Sreij et al.
Miller Fisher Syndrome With an Electrophysiologic Phenotype of Sensory Neuronopathy [0.03%]
米勒费舍综合征伴有神经电生理检测感觉神经元病特点
James B Meiling,Nicholas J Miller,James B Caress
James B Meiling
Making the Diagnosis With Neuromuscular Ultrasound: A Case of Intractable Lateral Antebrachial Cutaneous Nerve Pain After Phlebotomy [0.03%]
神经肌肉超声诊断一例静脉采血后难以缓解的前臂外侧皮神经痛病例报告
John Badir,Marisa Barclay McGhee,Gabriela A Velazquez
John Badir
An Initial Diagnosis of the Myopathic Form of Carnitine Palmitoyl Transferase Type II Deficiency Made in a 65-year-Old [0.03%]
一名65岁患者肉毒碱棕榈酰基转移酶II型缺乏症肌病样型的初步诊断
Floyd D Silva,Elina Zakin
Floyd D Silva
Progressive Acute Onset Demyelinating Polyneuropathy in a 64-Year-Old Man [0.03%]
一名64岁男性进行性急性脱髓鞘多发神经根病的病例报告
Seyed Jalaleddin Hadei,Bardiya Ghaderi Yazdi,Soroor Advani et al.
Seyed Jalaleddin Hadei et al.
Diagnostic Difficulty in a Girl With Anti-Signal Recognition Particle Myopathy With a Slow Progressive Course [0.03%]
以抗信号识别颗粒抗体致肌病为特点的缓慢进展性病例诊断过程复杂
Ken Imai,Takenori Nastume,Maki Shirai et al.
Ken Imai et al.
Ultrasonography of Recurrent Brachial Plexopathies in Hereditary Neuropathy With Liability to Pressure Palsies [0.03%]
遗传性神经病伴压力性瘫痪的复发性臂丛病变的超声影像学研究
James B Meiling,Araya Puwanant,Marisa Barclay Mcghee
James B Meiling