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BMC Neurology

Movement disorders

Section edited by Yih-Ru Wu

This section covers all types and aspects of movement disorders. Topics of include, but are not limited to, Parkinson's Disease, transcranial magnetic stimulation, spasticity, dyskinesia, movement disorders, rehabilitation and spinal cord injury.

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  1. Content type: Research article

    Spinocerebellar ataxia (SCA) subtypes are often caused by expansions in non-coding regions of genes like SCA8, SCA10, SCA12 and SCA36. Other ataxias are known to be associated with repeat expansions such as fragi...

    Authors: Gülsah Aydin, Gabriele Dekomien, Sabine Hoffjan, Wanda Maria Gerding, Jörg T. Epplen and Larissa Arning

    Citation: BMC Neurology 2018 18:3

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  2. Content type: Research article

    Individuals with cerebral palsy have smaller muscle volumes normalised to body mass than their typically developing peers. The aim of this study is to investigate the relationship between lower limb muscle vol...

    Authors: Jonathan J. Noble, Emily Chruscikowski, Nicola R. D. Fry, Andrew P. Lewis, Martin Gough and Adam P. Shortland

    Citation: BMC Neurology 2017 17:223

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  3. Content type: Research article

    Evaluation of speech disorders in PD taking into account sociodemographic conditions is not frequent. This paper aims to establish correlations between articulation disorders in PD patients and factors such as...

    Authors: Wioletta Pawlukowska, Karolina Skonieczna-Żydecka, Iwona Rotter, Krystyna Honczarenko and Przemysław Nowacki

    Citation: BMC Neurology 2017 17:221

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  4. Content type: Research article

    Real world data have an important role to play in the evaluation of epidemiology and burden of disease; and in assisting health-care decision-makers, especially related to coverage and payment decisions. Howev...

    Authors: Audrey Tanguy, Linus Jönsson and Lianna Ishihara

    Citation: BMC Neurology 2017 17:213

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  5. Content type: Research article

    The loss of the swallow-tail sign of the substantia nigra has been proposed for diagnosis of Parkinson’s disease. Aim was to evaluate, if the sign occurs consistently in healthy subjects and if it can be relia...

    Authors: Manuel A. Schmidt, Tobias Engelhorn, Franz Marxreiter, Juergen Winkler, Stefan Lang, Stephan Kloska, Philipp Goelitz and Arnd Doerfler

    Citation: BMC Neurology 2017 17:194

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  6. Content type: Case report

    Vacuolar protein sorting 35 (VPS35) was recently reported to be a genetic cause for late-onset autosomal dominant Parkinson’s disease (PD). However, VPS35 mutations are rarely reported in Asian populations. Herei...

    Authors: Ying-Fa Chen, Yung-Yee Chang, Min-Yu Lan, Pei-Lung Chen and Chin-Hsien Lin

    Citation: BMC Neurology 2017 17:191

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  7. Content type: Case report

    Frontotemporal degeneration (FTD) is a clinically and genetically heterogeneous neurodegenerative disorder characterized by deficits in executive function that frequently overlaps with parkinsonism and motor n...

    Authors: Hui-Chi Lin, Chin-Hsien Lin, Pei-Lung Chen, Shih-Jung Cheng and Pei-Hao Chen

    Citation: BMC Neurology 2017 17:186

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  8. Content type: Case report

    Huntington’s disease (HD) is an autosomal dominant disorder, typically characterized by chorea due to a trinucleotide repeat expansion in the HTT gene, although the clinical manifestations of patients with juv...

    Authors: Shi-Shuang Cui, Ru-Jing Ren, Ying Wang, Gang Wang and Sheng-Di Chen

    Citation: BMC Neurology 2017 17:152

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  9. Content type: Case report

    Spinal cord stimulation (SCS) has recently been reported to be effective for truncal postural abnormalities such as camptocormia and Pisa syndrome in Parkinson’s disease. In this case report, we describe a cas...

    Authors: Hisanao Akiyama, Saki Nukui, Masashi Akamatu, Yasuhiro Hasegawa, Osamu Nishikido and Soichiro Inoue

    Citation: BMC Neurology 2017 17:148

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  10. Content type: Research article

    Individuals with Cerebral Palsy (CP) present with sensorimotor dysfunction which make the control and execution of movements difficult. This study aimed to verify the speed-accuracy trade-off in individuals wi...

    Authors: Deborah Cristina Gonçalves Luiz Fernani, Maria Tereza Artero Prado, Talita Dias da Silva, Thais Massetti, Luiz Carlos de Abreu, Fernando Henrique Magalhães, Helen Dawes and Carlos Bandeira de Mello Monteiro

    Citation: BMC Neurology 2017 17:143

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  11. Content type: Research article

    Wilson’s disease (WD) is an autosomal recessive disorder of copper metabolism resulting in multifaceted neurological, hepatic, and psychiatric symptoms. The objective of the study was to comparatively assess t...

    Authors: Hanna M. Volpert, Jan Pfeiffenberger, Jan B. Gröner, Wolfgang Stremmel, Daniel N. Gotthardt, Mark Schäfer, Karl Heinz Weiss and Markus Weiler

    Citation: BMC Neurology 2017 17:140

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  12. Content type: Case report

    Parasomnia overlap disorder (POD) is a distinct parasomnia and characterized by concomitant manifestation of rapid-eye-movement (REM)- and non-REM (NREM)-parasomnias. Although not uncommon among patients with ...

    Authors: Panagiotis Bargiotas, Julia Muellner, W.M. Michael Schuepbach and Claudio L. Bassetti

    Citation: BMC Neurology 2017 17:137

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  13. Content type: Research article

    Parkinson’s disease is complicated by comorbidity and polypharmacy, but the extent and patterns of these are unclear. We describe comorbidity and polypharmacy in patients with and without Parkinson’s disease a...

    Authors: Gary McLean, John V. Hindle, Bruce Guthrie and Stewart W. Mercer

    Citation: BMC Neurology 2017 17:126

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  14. Content type: Case report

    Camptocormia is severe flexion of the thoracolumbar spine, exaggerated during standing and walking but minimized in supine position. Even though camptocormia is a relatively common condition during the course ...

    Authors: Yoon Kim, Ahro Kim, Aryun Kim and Beomseok Jeon

    Citation: BMC Neurology 2017 17:118

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  15. Content type: Research article

    Impulse control and related disorders (ICRDs) are clinically complications in Parkinson’s disease (PD). However, the clinical characteristics of ICRDs in Chinese PD patients were rarely reported. We aimed to e...

    Authors: Yu Zhang, An qi He, Lin Li, Wei Chen and Zhen guo Liu

    Citation: BMC Neurology 2017 17:98

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