Radiculopathy is sometimes evaluated with needle electromyography as additional examination to radiographic imaging. The purpose of this study was to determine the optimal needle electromyography protocol and the use of needle electromyography in the diagnosis of radiculopathy. The authors analysed English language writings from years 1981-2000. The selected studies reported a wide range of needle EMG abnormalities--from about 30 to 100% of pathological EMGs. That is caused by wide variety of patient populations and various EMG protocols. EMG of leg muscles in radiculopathy can consist of the assessment of the spontaneous activity only or be completed with the assessment of motor unit potential (MUP). The EMG of paraspinal muscles assesses spontaneous activity only. The number of abnormalities in needle EMG grows with the presence of characteristic radiculopathy symptoms, but positive EMG examinations are of importance only in cases where diagnosis is complicated. The rate of pathological results is higher when needle electromyography is used in the muscles of paraspinal region and extremities at the same time. The assessment of the spontaneous activity in extremity muscles alone minimizes the influence of error- causing factors on the EMG result. Nevertheless lack of assessment of motor units potentials makes electromyographic investigation of chronic radiculopathy impossible. Sensitivity and specificity of the method have to be determined before the clinical use of the assessment of MUP in chronic radiculopathy, especially in patients without motor weakness. Needle EMG abnormalities correlate with radiological findings in limited range as would be expected from the occurrence of radiological findings in asymptomatic patients and overlapping innervations of myotomes.
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Muscle Nerve
January 2025
International Collaboration on Repair Discoveries (ICORD), Vancouver, British Columbia, Canada.
Introduction/aims: Upper limb paralysis is arguably the most limiting consequence of cervical spinal cord injury (cSCI). There is limited knowledge regarding the early structural changes of muscles implicated in grasp/pinch function and upper extremity nerve transfer surgeries. We evaluated: (1) muscle size and echo intensity (EI) in subacute cSCI (2-6 months) and (2) the influence of lower motor neuron (LMN) damage on these ultrasound parameters.
View Article and Find Full Text PDFMuscle Nerve
January 2025
Service ENMG et de Pathologies Neuromusculaires, Centre de référence Des Maladies Neuromusculaires PACA-Réunion-Rhône Alpes, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, Bron, France.
Introduction/aims: Finger Extension Weakness and DOwnbeat Nystagmus Motor Neuron Disease (FEWDON-MND) is characterized by motor weakness predominantly affecting finger extension, accompanied by downbeat nystagmus. To date, only 11 patients have been reported. The present study adds a further three and aims to provide a more detailed description of the electrodiagnostic features of these patients.
View Article and Find Full Text PDFJ Neurol
January 2025
Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100070, China.
Background And Objective: Neuronal intranuclear inclusion disease (NIID) is a multifaceted disorder impacting both the central and peripheral nervous systems. This study aims to investigate the clinical and electrophysiological characteristics of peripheral neuropathy in patients with NIID.
Methods: In this cross-sectional study, patients diagnosed with NIID were prospectively recruited from multiple centers across China between October 2017 and May 2024.
NeuroSci
December 2024
Institute of Clinical Neurophysiology, Division of Neurology, University Medical Center Ljubljana, Zaloška cesta 7, 1525 Ljubljana, Slovenia.
In ulnar neuropathy at the elbow (UNE), the degree of neuropathic changes, the sensitivity of needle electromyography (EMG) in individual ulnar muscles, and the utility of individual EMG parameters are controversial. I compared qualitative needle EMG findings in two ulnar-innervated hands muscles and two ulnar-innervated forearm muscles in a group of previously reported UNE patients. Altogether, 170 UNE patients (175 arms) were studied.
View Article and Find Full Text PDFClin Neurophysiol
December 2024
Department of Clinical Neurophysiology, Vall d'Hebron University Hospital, Passeig de la Vall d'Hebron, 119, 08035 Barcelona, Spain. Electronic address:
Introduction/objective: Biallelic expansion of the pentanucleotide AAGGG in the RFC1- gene is associated with cerebellar ataxia, neuropathy, and vestibular areflexia syndrome (CANVAS). This study aimed to comprehensively characterise this condition by conducting an in-depth neurophysiological examination of afflicted patients.
Methods: A retrospective analysis was conducted in 31 RFC1-positive patients.
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