Multidimensional Phenotyping of Orthostatic Tremor and Orthostatic Myoclonus: Baseline Findings from a Longitudinal Clinical Study [0.03%]
体位性颤动和体位性肌阵挛的多维度表型特征：一项纵向临床研究的基线结果
Giridhar S Immanni,Anish Mehta,Prabhudev M Hiremath et al.
Giridhar S Immanni et al.
Background: Orthostatic tremor (OT) and orthostatic myoclonus (OM) are rare weight-bearing hyperkinetic disorders defined electrophysiologically but often overlap clinically. Prior studies were limited to small series wit...
Resilience Mitigates the Link between Adverse Childhood Experiences and Musician's Dystonia: A Neuroendocrine and Psychological Perspective [0.03%]
韧性缓解了不良童年经历与音乐家肌张力障碍之间的联系：神经内分泌和心理视角
Julian Burek,Stine Alpheis,Christopher Sinke et al.
Julian Burek et al.
Background: Musician's dystonia (MD) is a task-specific movement disorder affecting up to 1% of all professional musicians. Although adverse childhood experiences (ACEs) have been proposed as risk factors, the etiology of...
Clinical Characteristics of Primary Orthostatic Tremor - a Comprehensive Clinical Assessment of Patients in Sweden [0.03%]
原发性直立性震颤的临床特征——瑞典患者的全面临床评估
Karolina Af Edholm,Mathias Sundgren,Erik Fransén et al.
Karolina Af Edholm et al.
Background: Primary orthostatic tremor (POT) is a rare neurological disease presenting as a bilaterally coherent tremor of 13-18 Hz and a subjective sensation of unsteadiness while standing. Patients are severely affected...
Clinical, Radiological, and Genetic Profile of Patients with FA2H-Associated Neurodegeneration: Eight Cases from India and a Review of the Literature [0.03%]
FA2H相关神经退行性疾病的临床、影像和遗传特征：来自印度的8例及文献复习
Vikram V Holla,Riyanka Kumari,Neeharika Sriram et al.
Vikram V Holla et al.
Background: Autosomal recessive spastic paraplegia 35 (SPG35), also known as Fatty acid hydroxylase-associated neurodegeneration (FAHN), is a rare recessive neurodegenerative disorder with or without ataxia, dystonia, and...
Sanuri Gunawardena,Umar Shuaib,Junaid Siddiqui
Sanuri Gunawardena
Background: Sensory ganglionopathy is a rare, often underrecognized neurological manifestation of Sjogren's disease, presenting with non-length-dependent sensory symptoms that may mimic other neuropathies. ...
Pseudoathetotic Pseudodystonia as a Manifestation of Isolated Medullary Demyelination in Neuromyelitis Optica Spectrum Disorder [0.03%]
神经免疫病视神经脊髓炎谱系疾病的单发延髓脱髓鞘的临床表现：假手足徐动chtenhausen综合征报告病例
Prachi Mohapatra,Lekshmi Sambhu Hema,Aditya Mahadevan et al.
Prachi Mohapatra et al.
Background: Pseudoathetosis and pseudodystonia are rare sensory-driven hyperkinetic movement disorders that may mimic primary dystonia. Although these manifestations have been reported in neuromyelitis optica spectrum dis...
Clinical, Radiological, and Genetic Profiles of Eight Patients with Combined Dystonic Manifestation of Type-III GM1 Gangliosidosis: A Video Case Series from India [0.03%]
GM1糖脂贮积病Ⅲ型合并 dystonic 表现的临床、影像及基因特点：来自印度的 8 例视频病例报告
Subhajit Roy,Cheshta Arora,Vikram V Holla et al.
Subhajit Roy et al.
Background: Type-III (adult/chronic) GM1 gangliosidosis is an uncommon, late-onset lysosomal disorder that frequently presents as a complex movement disorder. ...
Rescue Thalamotomy for Habituation to Deep Brain Stimulation in Essential Tremor: Case Report [0.03%]
病例报告：丘脑毁损治疗原发性震颤患者对深部脑刺激电极适应综合征
Roman Kiselev,Vladislav Babchenko
Roman Kiselev
Background: Habituation to deep brain stimulation (DBS) remains a therapeutic challenge in essential tremor (ET), with 4-42% of patients experiencing progressive loss of benefit. ...
Generalized Dystonia in a Patient With Wilson Disease 5 Years After Liver Transplant: A Case Report [0.03%]
一例肝移植术后5年威尔森病患者出现偏侧抽动的病例报告
Elise Edwards,Benjamin Coleman,Matthew Feldman et al.
Elise Edwards et al.
Background: Liver transplant (LT) is considered curative for Wilson disease (WD) with hepatic failure refractory to medical therapy, particularly when neurologic symptoms are absent. ...
Miranda Medeiros,Calwing Liao,Allison A Dilliott et al.
Miranda Medeiros et al.
Background: Essential tremor (ET) is a complex neurological disorder with a strong genetic basis, yet there remains a disparity between its estimated heritability and currently known genetic risk. This missing heritabilit...