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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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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
Veit Mylius,Jan Harald Baars,Karsten Witt et al. Veit Mylius et al.
Dopamine exerts antinociceptive effects on pain in PD at cortical and spinal levels, whereas only cortical effects have been described for DBS, so far. By assessing the nociceptive flexion reflex (NFR) threshold at medication on, and DBS ON...
Dani J Kim,Ana L Isidro-Pérez,Michelle Doering et al. Dani J Kim et al.
Background: Parkinson's disease (PD) is a rapidly growing neurodegenerative disorder, but up-to-date epidemiological data are lacking in Latin America. We sought to estimate the prevalence and incidence of PD and parkinso...
James A Brissenden,Teresa Scerbak,Roger L Albin et al. James A Brissenden et al.
Background: Impaired movement vigor (bradykinesia) is a cardinal feature of Parkinson's disease (PD) and hypothesized to result from abnormal motivational processes-impaired motivation-vigor coupling. Dopamine replacement...
Eleonora Fiorenzato,Sadaf Moaveninejad,Luca Weis et al. Eleonora Fiorenzato et al.
Background: Higuchi's fractal dimension (FD) captures brain dynamics complexity and may be a promising method to analyze resting-state functional magnetic resonance imaging (fMRI) data and detect the neuronal interaction ...
Ilaria Quartesan,Elisa Vegezzi,Riccardo Currò et al. Ilaria Quartesan et al.
Background: Biallelic intronic AAGGG repeat expansions in the replication factor complex subunit 1 (RFC1) gene were identified as the leading cause of cerebellar ataxia, neuropathy, vestibular areflexia syndrome. Patients...
Flávio Moura Rezende Filho,Neringa Jurkute,João Brainer Clares de Andrade et al. Flávio Moura Rezende Filho et al.
Background: ATXN2 is the causative gene of spinocerebellar ataxia type 2 (SCA2) and has been implicated in glaucoma pathogenesis. Therefore, studying ocular changes in SCA2 could uncover clinically relevant changes. ...
Isaac Bul Deng,Jordan Follett,Mengfei Bu et al. Isaac Bul Deng et al.
Recent studies show that pathogenic variants in DNAJC12, a co-chaperone for monoamine synthesis, may cause mild hyperphenylalaninemia with infantile dystonia, young-onset parkinsonism, developmental delay and cognitive deficits. DNAJC12 has...
Shan V Andrews,Prashanth L Kukkle,Ramesh Menon et al. Shan V Andrews et al.
Background: Recent studies have advanced our understanding of the genetic drivers of Parkinson's disease (PD). Rare variants in more than 20 genes are considered causal for PD, and the latest PD genome-wide association st...