Craniocervical instability after inadvertent neck hyperextension in Ehlers-Danlos syndrome: a retrospective case series and literature review [0.03%]
血管性埃勒斯-当洛斯综合征患者意外出现颈椎过度伸展后的颅颈不稳的病例回顾及文献综述
Chanbin Lee,Stephanie Sutherland,Pradeep Chopra
Chanbin Lee
Changes in cognitive performance following combined CogSMART-SA and BrainHQ interventions: a pilot study [0.03%]
结合CogSMART-SA和BrainHQ干预后认知表现的变化：一项试点研究
Hetta Gouse,Zanele Nhlabatsi-Khumalo,Rhiannon Chernotsky et al.
Hetta Gouse et al.
Effects of anemia on short-term prognosis and imaging features of patients with acute ischemic stroke: preliminary findings [0.03%]
贫血对急性缺血性卒中的短期预后和影像学特征的影响：初步研究发现
Bingqing Zhao,Ying Chen,Ye Yuan et al.
Bingqing Zhao et al.
Neuronal intranuclear inclusion disease caused by NOTCH2NLC gene expansion: a case report and literature review [0.03%]
NOTCH2NLC基因异常所致神经元细胞核内包涵体病1例及文献复习
Linsen Ye,Yue Xu,Shuqing Meng et al.
Linsen Ye et al.
Retrospective case series of peripheral neuropathy following carbon monoxide poisoning: clinical and electrophysiological characteristics [0.03%]
一氧化碳中毒后外周神经病的病例系列分析：临床和电生理特征
Zongyan Ma,Yanni Duan,Xingxing Huang et al.
Zongyan Ma et al.
Treatment patterns and adverse events of antiseizure medications among adult patients with epilepsy: a single centre observational cross-sectional study in Northern Sri Lanka [0.03%]
斯里兰卡北部单一中心成人癫痫患者抗癫痫药物治疗模式和不良事件的观察性横断面研究
Yalini Guruparan,Ajantha Keshavaraj,Thiyahiny S Navaratinaraja
Yalini Guruparan
A case of isolated brainstem bright spotty lesion in a patient with AQP4-positive NMOSD [0.03%]
一名AQP4阳性NMOSD患者的孤立脑干亮点病变的病例报告
Chloé Froidevaux,Corentin Provost,Nicolas Mélé
Chloé Froidevaux
A new MYH2 variant in an Italian patient expanding the clinical spectrum of MYH2-related myopathy [0.03%]
意大利患者中的一个新的MYH2变异体扩大了与MYH2相关的肌病的临床谱系
Simona Zanotti,Dario Ronchi,Laura Napoli et al.
Simona Zanotti et al.
A novel STUB1 p.(Gln118*) nonsense variant in compound heterozygosity causes autosomal recessive spinocerebellar ataxia type 16 in a Chinese patient [0.03%]
在中国一名患者中，STUB1新的p.(Gln118*)终止变异与复合杂合性导致的常染色体隐性脊小脑共济失调16型
Kun-Mu Zheng,Ming-Kun Tang,Jian-Peng Li et al.
Kun-Mu Zheng et al.