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期刊名:Movement disorders

缩写:MOVEMENT DISORD

ISSN:0885-3185

e-ISSN:1531-8257

IF/分区:7.6/Q1

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共收录本刊相关文章索引7165
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Fatemeh Vazirian,Jing Tian,Jane Alty et al. Fatemeh Vazirian et al.
Background: Chronic musculoskeletal pain often co-occurs with Parkinson's disease (PD); however, whether individuals with chronic pain have a higher risk of developing PD is unclear. ...
Stacha F I Reumers,Roderick P P W M Maas,Dennis J L G Schutter et al. Stacha F I Reumers et al.
Background: The cerebellar cognitive affective syndrome (CCAS) encompasses cognitive and affective symptoms in patients with cerebellar disorders, for which no proven treatment is available. ...
Shiro Horisawa,Ryo Saito,Bohui Qian et al. Shiro Horisawa et al.
Background: No clinical trials have been reported on the use of focused ultrasound (FUS) for treating cervical dystonia. Objective: We ...
Shan Cao,Xiang Fang,Jianwen Wang et al. Shan Cao et al.
Background: High positivity rate of skin phosphorylated α-synuclein (P-SYN) was observed in Parkinson's disease (PD). Bullous pemphigoid (BP) is one of the most common autoimmune skin diseases associated with PD. ...
Massimiliano Germani,Irene Rebollo Mesa,Tim J Buchanan et al. Massimiliano Germani et al.
Background: Progressive supranuclear palsy (PSP) is a rare and fatal neurodegenerative disorder for which there are currently no disease-modifying treatments. Recent trials of potential therapies had durations of 12 month...
Yan Shi,Junhao Xie,Junyi Jiang et al. Yan Shi et al.
Background: Hereditary spastic paraplegia (HSP) is characterized by progressive lower limb weakness and spasticity, with unknown genetic cause in many cases. ...
Nicole Calakos,Michael Zech Nicole Calakos
Advances in genetic technologies and disease modeling have greatly accelerated the pace of introducing and validating molecular-genetic contributors to disease. In dystonia, there is a growing convergence across multiple distinct forms of t...
Mandy Radefeldt,Sabrina Lemke,Kridsadakorn Chaichoompu et al. Mandy Radefeldt et al.
Background: The p.Ser71Arg RAB32 variant was recently associated with Parkinson's disease (PD). Objective: The aim was to investigate t...