Results 31 to 40 of about 26,795 (236)
Clinical Neurophysiology Practice, 2022 Objective: We investigated how clinical neurophysiological testing can help distinguish tremor and myoclonus and their subtypes. Methods: We retrospectively analysed clinical and neurophysiological data from patients who had undergone polymyography (EMG +
Cheryl S.J. Everlo +3 more
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EEG–EMG polygraphic study of dystonia and myoclonus in a case of Creutzfeldt–Jakob disease
Epilepsy and Behavior Case Reports, 2015 We report on a patient with sporadic Creutzfeldt–Jakob disease (CJD) who showed dystonia, periodic myoclonus, and periodic sharp wave complexes (PSWCs) on EEG.
Takao Hashimoto +4 more
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Memantine-induced Myoclonus in a Patient with Alzheimer Disease
Tremor and Other Hyperkinetic Movements, 2015 Background: Myoclonus can be a clinical manifestation of numerous neurodegenerative disorders and an adverse drug reaction to medications used in their treatment.Case report: Herein, we report memantine-induced myoclonus in a patient with Alzheimer ...
Aditya A. Murgai, Mark S. LeDoux
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Dexmedetomidine versus Lignocaine in the Prevention of Etomidate-induced Myoclonus- A Randomised Double-blinded Study [PDF]
Journal of Clinical and Diagnostic Research, 2023 Introduction: Etomidate is a preferred induction agent owing to its stable haemodynamic profile, minimal respiratory side-effects, minimal histamine release, cerebral protection and its property of rapid onset and short duration.
Gojendra Rajkumar +7 more
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Myoclonus-Dystonia/Essential Myoclonus
, 2010 Myoclonus-dystonia (M-D, formerly known as 'Hereditary essential myoclonus') is a rare movement disorder characterized by myoclonic jerks and dystonic movements or postures.
Tijssen, M. A. J. +3 more
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Zonisamide‐responsive myoclonus in SEMA6B‐associated progressive myoclonic epilepsy
Annals of Clinical and Translational Neurology, 2021 We present a female patient in her early twenties with global development delay, progressive ataxia, epilepsy, and myoclonus caused by a stop mutation in the SEMA6B gene.
Rebecca Herzog +7 more
doaj +1 more source
, 2023 Myoclonus is often approached in different ways by epileptologists and movement disorder specialists, leading to confusion in the literature. Multiplicity and inconsistency over the past 2 centuries resulted in a lack of precision and ambiguity of the ...
Sterre Van Der Veen +5 more
core +1 more source
“Dancing belly” in an old diabetic lady
Journal of Family Medicine and Primary Care, 2020 Movement disorder, although rare, is increasingly being recognized as the initial presenting sign of the hyperglycemic state. Although chorea-ballism has frequently been reported among diabetics, monoballism is a very rare phenomenon.
Souvik Dubey +6 more
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A Rare Neurological Complication of Ranolazine
Case Reports in Neurological Medicine, 2013 Myoclonus is not a known side effect of ranolazine. We report a case of myoclonus in a 72-year-old female who underwent cardiac catheterization for angina and was started on ranolazine after the procedure. Two days after ranolazine therapy on 1000 mg per
Jahan Porhomayon +2 more
doaj +1 more source
Mycoplasma pneumoniae associated opsoclonus-myoclonus syndrome in three cases [PDF]
, 2010 Opsoclonus-myoclonus syndrome (OMS) is a rare acquired movement disorder occurring in all age groups, predominantly in infants. Although the exact pathogenesis is still undefined, there is strong evidence for a paraneoplastic or parainfectious immune ...
Aebi, Christoph +4 more
core +1 more source