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pro vyhledávání: '"Sacha E. Gandhi"'
Publikováno v:
Advances in Clinical Neuroscience & Rehabilitation, Vol , Iss (2022)
Dystonia is a hyperkinetic movement disorder (HMD), characterised by sustained or intermittent involuntary muscle contractions resulting in abnormal postures and / or movements [1]. Although primary dystonia has an estimated prevalence of 16 per 100,
Externí odkaz:
https://doaj.org/article/21872356eb074933b7ce182c1e881ee0
Publikováno v:
Practical Neurology. 23:257-260
Autor:
Ana Töpf, Kathryn M. Brennan, Willie Stewart, Kevin Kinch, Rosaline Quinlivan, Cheryl Longman, Volker Straub, Sacha E. Gandhi, Richard E. Petty, Maria Elena Farrugia
Publikováno v:
Neuromuscular Disorders. 31:695-700
This retrospective study evaluated the phenotypic and genotypic features of 14 patients with McArdle disease attending the West of Scotland adult muscle clinic. Although all patients experienced exercise-induced cramps, exercise intolerance and hyper
Publikováno v:
Practical neurology. 20(4)
Movement disorders are typically perceived as being gradually progressive conditions that are managed in outpatient settings. However, they may manifest de novo with an acute severe phenotype or an acute decompensation. A movement disorder becomes an
Publikováno v:
Gandhi, S E, Silverdale, M A, Mercer, D, Marshall, A G & Kobylecki, C 2020, ' Real world use of a neurophysiology service for the differential diagnosis of hyperkinetic movement disorders ', Parkinsonism & Related Disorders, vol. 71, pp. 11-14 . https://doi.org/10.1016/j.parkreldis.2020.01.003
INTRODUCTION: Clinical neurophysiology constitutes a potentially useful aid in differentiating hyperkinetic movement disorders (HMD). Parameters including presence of a Bereitschaftspotential on back-averaged electroencephalography (EEG) have been de
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 90:e35.2-e35
Neurophysiology constitutes a potentially useful aid in differentiating hyperkinetic movement disorders (HMD). Parameters including presence of a Bereitschaftspotential on back-averaged EEG have been demonstrated to help distinguish between these dis
Autor:
Vicky L Marshall, Sacha E Gandhi
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 90:e37.4-e38
Idiopathic Parkinson’s disease (IPD) is typically insidious in onset and gradually progressive. Acute onset Parkinsonism is, conversely, a rare entity. It may be attributable to rapid onset dystonia parkinsonism; post-encephalitic sequelae; vascula
Publikováno v:
Parkinsonism & Related Disorders. 20:265-266