Separation of stroke from vestibular neuritis using the video head impulse test: machine learning models versus expert clinicians [0.03%]
视频头脉冲测试区分中风与前庭神经炎：机器学习模型和专家医生的对比
Chao Wang,Jeevan Sreerama,Benjamin Nham et al.
Chao Wang et al.
Background: Acute vestibular syndrome usually represents either vestibular neuritis (VN), an innocuous viral illness, or posterior circulation stroke (PCS), a potentially life-threatening event. The video head impulse tes...
Overlapping presence of β-amyloid, tau, p-tau, and α-synuclein in skin nerve fibers in Alzheimer's disease [0.03%]
阿尔茨海默病皮肤神经纤维中β-淀粉样蛋白、tau、p-tau和α-突触核蛋白的重叠存在
Emilie Buchholz,Marie-Luise Machule,Maria Buthut et al.
Emilie Buchholz et al.
Objective: Skin nerve fiber deposition of proteins can be strongly associated with neurodegenerative diseases, such as phosphorylated α-synuclein (p-SN) in synucleinopathies. Little is known about other neurodegenerative...
Heterogeneity of cognitive progression and clinical predictors in Parkinson's disease-subjective cognitive decline [0.03%]
帕金森病的主观认知下降的认知进展异质性和临床预测因子
Jon Rodríguez-Antigüedad,Saül Martínez-Horta,Arnau Puig-Davi et al.
Jon Rodríguez-Antigüedad et al.
Predictors of achieving minimal manifestations or better status in ocular myasthenia gravis with immunotherapy [0.03%]
免疫治疗在眼肌无力症中达到最小表现或更好状态的预测因素
Teppei Komatsu,Haruhiko Motegi,Masahiro Mimori et al.
Teppei Komatsu et al.
Background: Ocular myasthenia gravis (MG), while less severe than generalized MG, significantly impairs quality of life due to its impact on vision and daily activities. Immunotherapy is a key treatment, yet the optimal t...
Earshad Mia,Khalid Hamandi
Earshad Mia
Prevalence of infratentorial superficial siderosis in a large general population sample from the UK Biobank [0.03%]
来自英国生物银行的大一般人群中幕下脑浅表含铁血黄素沉积症的流行率
N Kharytaniuk,D Hikmat,H Ozkan et al.
N Kharytaniuk et al.
Background: Classical infratentorial superficial siderosis (iSS) is considered a rare but potentially disabling neurological disorder. It results from slow chronic blood extravasation into the cerebrospinal fluid and depo...
Observational Study
Journal of neurology. 2025 Mar 4;272(3):242. DOI:10.1007/s00415-025-12965-w 2025
Deep characterization of females with heterozygous Duchenne muscular dystrophy mutations [0.03%]
杜兴氏肌肉营养不良突变杂合女性的深度表征
Pietro Riguzzi,Daniele Sabbatini,Aurora Fusto et al.
Pietro Riguzzi et al.
Objective: Duchenne muscular dystrophy (DMD) is an X-linked muscular dystrophy due to null mutations in the DMD gene that predominantly affects males, while heterozygous females are usually asymptomatic carriers. In appro...
Observational Study
Journal of neurology. 2025 Mar 4;272(3):244. DOI:10.1007/s00415-025-12987-4 2025
Tick-borne encephalitis in adults in Denmark: a nationwide prospective cohort study from 2015 to 2023 [0.03%]
丹麦成人中的蜱传脑炎：2015年至2023年的全国前瞻性队列研究
Anna Maria Florescu,Thomas Bryrup,Carsten Schade Larsen et al.
Anna Maria Florescu et al.
Background: Our aim was to characterize the clinical presentation and outcome in adults with tick-borne encephalitis (TBE) and to determine the incidence and test activity of TBE in Denmark. ...
Early onset sleep disorders predict severity, progression and death in multiple system atrophy [0.03%]
早期睡眠障碍可预测多系统萎缩的严重程度、进展和死亡
Giulia Giannini,Luca Baldelli,Federica Provini et al.
Giulia Giannini et al.
Background: Early stridor onset (≤ 3 years from disease onset) is a predictor of shorter survival in Multiple System Atrophy (MSA), but its role on disease progression is not yet established. In MSA, previous studies on ...
Outcomes of deep brain stimulation surgery in the management of dystonia in glutaric aciduria type 1 [0.03%]
戊二酸血症I型 dystonia深部脑刺激手术的疗效研究
Daniel E Lumsden,Stavros Tsagkaris,Jon Cleary et al.
Daniel E Lumsden et al.
Objectives: Glutaric aciduria type 1 (GA1) is a rare autosomal recessive organic acidaemia caused by deficiency of the glutaryl-CoA dehydrogenase enzyme. We describe the outcomes following deep brain stimulation (DBS) for...