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1

K, Silver Julie, and Weiss Jay, eds. Easy EMG: A guide to performing nerve conduction studies and electromyography. Butterworth-Heinemann, 2004.

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2

Edmonds, Harvey L. Computerized EMG monitoring in anesthesia and intensive care. MP, 1988.

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3

1962-, Greenberg Steven A., and Amato Anthony A. 1960-, eds. EMG pearls. Hanley & Belfus, 2004.

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4

J, Robinson William. The effects of skill level on EMG activity during internal and external imagery. Microform Publications, College of Human Development and Performance, University of Oregon, 1985.

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5

M. P. van der Grinten. Preventie beroepsgebonden problematiek van het bewegingsapparaat: Inventarisatie en beoordeling van in het veld bruikbare methoden voor het registreren van "elektrische spieractiviteit" (EMG) en het "ervaren belasting". Directoraat-Generaal van de Arbeid van het Ministerie van Sociale Zaken en Werkgelegenheid, 1990.

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6

Shahani, Bhagwan T. Electromyography in Cns Disorders: Central Emg. Butterworth-Heinemann, 1985.

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7

Shahani, Bhagwan T. Electromyography in CNS Disorders: Central EMG. Elsevier Science & Technology Books, 2014.

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8

Amero, Dino. Coloring Book - You Will Get Better - Electromyography EMG. Independently Published, 2021.

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9

Bairagi, Vinayak, and Archana Bajirao Kanwade. Chronic Obstructive Pulmonary Disease (COPD) Diagnosis Using Electromyography (EMG). Elsevier Science & Technology Books, 2022.

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10

Chronic Obstructive Pulmonary Disease (COPD) Diagnosis Using Electromyography (EMG). Elsevier, 2022. http://dx.doi.org/10.1016/c2020-0-03143-9.

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11

Lahoda, Frieder, Arno Ross, Walter Issel, A. Schrader, and J. Payan. EMG Primer: A Guide to Practical Electromyography and Electroneurography. Springer London, Limited, 2012.

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12

Bairagi, Vinayak, and Archana Bajirao Kanwade. Chronic Obstructive Pulmonary Disease (COPD) Diagnosis Using Electromyography (EMG). Elsevier Science & Technology, 2022.

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13

Silver, Julie K., Jay M. Weiss, and Lyn Weiss. Easy EMG: A Guide to Performing Nerve Conduction Studies and Electromyography. Elsevier - Health Sciences Division, 2015.

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14

Katirji, Bashar. Electromyography in Clinical Practice. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190603434.001.0001.

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Clinical Electromyography in Clinical Practice provides case-based learning of clinical Electromyography (EMG) with a main mission of reducing the gap between theory and practice in the field of electrodiagnostic medicine. The book format includes four introductory chapters that acquaint the discipline and scope of the EMG Examination to the beginners. This include chapters on nerve conduction studies, needle EMG, and specialized testing including late responses, repetitive nerve stimulation and single fiber EMG. Discussion on the electrodiagnostic and clinical EMG findings in the numerous neu
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15

Stålberg, Erik. Electromyography. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199688395.003.0007.

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Electromyography (EMG) has been used since the 1940s in the diagnosis of neuromuscular disorders. It has particularly developed with the advent of computers and recording equipment with integrated software. This has made methods of analysis fast, robust, and precise, helping to deal with increasing numbers of patients. Indications have changed dynamically over the years, with the development of new EMG methods themselves and complementary methods used in this field for diagnosis such as histochemistry, genetics, and imaging techniques. This chapter focuses mainly on the routine methods based o
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16

Silver, Julie K., Lyn D. Weiss, and Jay M. Weiss. Easy EMG: A Guide to Performing Nerve Conduction Studies and Electromyography. Elsevier, 2022.

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17

Weiss, Lyn D. Easy EMG: A Guide to Performing Nerve Conduction Studies and Electromyography. Media Alternatives, INC., 2022.

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18

Pitt, Matthew. Paediatric Electromyography. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198754596.001.0001.

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Paediatric Electromyography is a single-author textbook which covers the full range of applications of the techniques of nerve conduction and electromyography (EMG) in children from the neonatal period to the late teenage years. It comprises five sections. Section 1 in its first chapter, gives a detailed introduction to the different skills that are needed to effect successful interventions in paediatric EMG. The emphasis here is that paediatric EMG is not simply adult EMG applied to younger subjects. Its second chapter is an introduction to the basic physiology which is common to any practice
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19

Klein, Cliff S., Sheng Li, Xiaogang Hu, and Xiaoyan Li, eds. Electromyography (EMG) Techniques for the Assessment and Rehabilitation of Motor Impairment Following Stroke. Frontiers Media SA, 2019. http://dx.doi.org/10.3389/978-2-88945-853-0.

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20

Fuglsang-Frederiksen, Anders, Kirsten Pugdahl, and Hatice Tankisi. Quantitative electromyography. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199688395.003.0008.

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Several quantitative electromyography (QEMG) methods are used for diagnosing and monitoring in patients with neuromuscular disorders. At weak effort of the muscle, motor unit potential (MUP) analyses as individual MUP, multi-MUP, and macro-EMG are diagnostically sensitive and well tested. At higher effort of the muscle, interference pattern analyses such as the turns amplitude analysis are also diagnostically sensitive. Other potential diagnostic methods are power spectrum analysis, muscle fibre conduction velocity analysis, and some surface EMG methods. In patients with myopathy, QEMG has an
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21

Pitt, Matthew. Paediatric conditions. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199688395.003.0025.

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This chapter dedicated to the practice of paediatric electromyography starts with a consideration of some of the misconceptions under which this particular investigation labours. The relevant technical aspects and normative data are discussed along with the personal characteristics needed. Sections cover the investigative strategies that need to be employed, the hereditary and acquired conditions that are common reasons for referral for electromyography (EMG), following an anatomical template, and conditions in which EMG has a particular role. The use of stimulation single fibre EMG in the dia
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22

Katirji, Bashar. The Scope of the EMG Examination. Edited by Bashar Katirji. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190603434.003.0001.

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Clinical electromyography (EMG) refers to the diagnostic tool in the electrophysiological evaluation of disorders of peripheral nerve and muscle. This introductory chapter defines the terms of the discipline and its scope. Clinical EMG used in the evaluation of Clinical EMG is utilized by a variety of physicians, including specialists in the field of neurology, physical medicine and rehabilitation, orthopedics, hand surgery, neurosurgery, spine, rheumatology and pain management. The scope of the EMG Examination includes nerve conduction studies and needle EMG. It also includes other specialize
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23

Cohen, Jeffrey A., Justin J. Mowchun, Victoria H. Lawson, and Nathaniel M. Robbins. A 40-Year-Old Female with Increasing Arm Pain and Numbness. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190491901.003.0013.

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Neurogenic thoracic outlet syndrome (NTOS) is an uncommon cause of chronic arm pain and numbness but should not be missed. It can lead to chronic pain and disability. Symptoms of NTOS are often aggravated by arm exertion and elevation and tend to occur after exercise rather than activity. A thorough diagnostic evaluation is key, which includes provocative tests, imaging, electromyography/nerve conduction study, and diagnostic injections. Electromyography/nerve conduction study (EMG/NCS) are recommended for NTOS as it is important to exclude an entrapment neuropathy or cervical radiculopathy th
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24

Pitt, Matthew. Needle EMG findings in different pathologies. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198754596.003.0007.

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In this chapter, the inability of electromyography (EMG) to be able to further progress the diagnosis of myopathy on its own—requiring muscle biopsy and other modalities such as genetics to complete this process—is emphasized. The role of EMG particularly in the era of genetics is discussed. Findings in neurogenic abnormality are next described and the important hereditary conditions such as spinal muscular atrophy (SMA), distal SMA, Brown–Vialetto–Van Laere syndrome, segmental anterior horn cell disease, conditions with progressive bulbar palsy, SMARD1, and pontocerebellar hypoplasia with spi
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25

Misra, V. Peter, and Santiago Catania. EMG-guided botulinum toxin therapy. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199688395.003.0026.

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This chapter explains the mechanism by which botulinum neurotoxin (BoNT) causes its neuromuscular paralytic effects, and reviews the developments that led these effects to be harnessed therapeutically. It specifically focuses upon the conditions of dystonia and spasticity. Within the spectrum of these diseases, it discusses those situations where BoNT injections are the treatment of choice. The very accurate targeting of BoNT into specific muscles in many situations is both desirable and crucial in some situations BoNT’s therapeutic neuroparalytic effect may need to be restricted to a single m
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26

Kimura, Jun, and Jeffrey A. Strakowski. Electrodiagnosis in Diseases of Nerve and Muscle. 5th ed. Oxford University PressNew York, 2025. https://doi.org/10.1093/med/9780197658017.001.0001.

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Abstract Electrodiagnosis in Diseases of Nerve and Muscle: Principles and Practice provides an overview of electromyography (EMG) and electrodiagnosis. It discusses the key concepts of nerve conduction studies, electromyography, intraoperative monitoring, and somatosensory and motor evoked potential. Jun Kimura’s fifth edition of Electrodiagnosis in Diseases of Nerve and Muscle offers a comprehensive text on electromyography that will be useful to both beginning practitioners and experts alike. The fifth edition is expected to be important as a world-class reference in the subspecialty of neur
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27

Pitt, Matthew. Introduction. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198754596.003.0001.

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This chapter opens with a discussion of how paediatric electromyography (EMG) is materially different from that performed in adults. In this chapter, the recognition that EMG is considered a painful experience is acknowledged. The techniques to reduce this discomfort and the associated anxiety are described, including preparation of the children, both prior to the test and during the clinic appointment itself. The order of testing is another important factor along with the need for every intervention having a clear reason for its use. In other parts of the world, sedation is considered an esse
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28

Pitt, Matthew. More advanced techniques. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198754596.003.0012.

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This chapter covers some of the less common, more advanced techniques which will be demanded of the paediatric electromyographer. Diaphragmatic function can be assessed by phrenic nerve studies with, on occasion, additional information from diaphragmatic electromyography (EMG) approached from the transcostal route. Tests of cranial nerves are covered including blink reflexes, and studies that can be used for the investigation of swallowing and sucking abnormalities. Also discussed are investigations for abnormalities of the face including congenital facial palsy either acquired congenitally or
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29

Ramdass, Ranjit. Neurophysiology in the assessment of inflammatory myopathies. Edited by Hector Chinoy and Robert Cooper. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198754121.003.0015.

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Clinical neurophysiology (electrodiagnosis) includes the assessment of peripheral nerves by electrical stimulation (nerve conduction studies, NCS) and needle examination of muscles (electromyography, EMG). Electrodiagnostic assessment is a functional extension of clinical examination into the laboratory. It plays an important role in the investigation of a patient suspected of having myositis, providing valuable information regarding peripheral nerve, neuromuscular junction and muscle functions, to better characterize clinical syndromes. NCS can establish the presence and quantify the severity
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30

Mills, Kerry R. Disorders of single nerves, roots, and plexuses. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199688395.003.0021.

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The role of electromyography (EMG) and nerve conduction studies in disorders of single nerve, root, and plexus lesions are discussed. The motor and sensory anatomy underpinning diagnosis is described and a scheme presented showing the key muscles to be examined using EMG to differentiate nerve, plexus, and root lesions. The main causes of mononeuritis multiplex, of either axonal degeneration or demyelinative pathology, are covered, including diabetic neuropathy, vasculitic neuropathy, multifocal motor neuropathy with block, and the Lewis–Sumner syndrome. The confirmatory role of EMG and nerve
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31

Shaibani, Aziz. Muscle Atrophy and Hypertrophy. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190661304.003.0017.

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Muscle atrophy is usually caused by interruption of axonal flow [axonal neuropathies, motor neuron diseases (MNDs), etc.]. If weakness is out of proportion to atrophy, demyelinating neuropathy should be suspected. Chronic myopathies and immobility also may cause atrophy, but no electromyography (EMG) evidence of denervation or myopathy is found. The pattern of atrophy is often helpful to localize the lesions. Atrophy of the interossi and preservation of the bulk of the thenar muscles suggest ulnar neuropathy, but atrophy of both would suggest a C8 or plexus pathology. Muscle enlargement may be
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32

Cohen, Jeffrey A., Justin J. Mowchun, Victoria H. Lawson, and Nathaniel M. Robbins. A 54-Year-Old Male with Right-Hand Weakness. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190491901.003.0002.

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Early in its course, amyotrophic lateral sclerosis (ALS) is mistaken for a number of other neuromuscular problems, including spinal disease, multifocal motor neuropathy, and even carpal tunnel syndrome (CTS) when the weakness is distal and focal. In our patient CTS or cervical spine disease was considered. MRI scan of the appropriate spinal level is important to rule out spinal disease. Nerve conduction studies (NCS) and electromyography (EMG) help to exclude other possibilities and point to the diagnosis of ALS. Later in the clinical course, the clinical picture is pathognomonic with upper an
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33

Pohlman, Dane, Victor Tseng, and Eric Wisotzky. Pocket EMG. Springer Publishing Company, Incorporated, 2014.

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34

Kennett, Robin P., and Sidra Aurangzeb. Primary muscle diseases. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199688395.003.0024.

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This chapter on primary muscle diseases explains how analysis of compound muscle action potential (CMAP) amplitude, abnormal spontaneous activity on needle electromyography (EMG), and motor unit action potentials (MUAP) characteristics may be used to give an indication of pathophysiological processes, and goes on to describe the combination and distribution of abnormalities that may be expected in the more commonly encountered myopathies. The conditions considered in detail are inflammatory myopathy (including myositis), critical illness myopathy, disorders with myotonia, inherited myopathy (i
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35

Michell, Andrew. Understanding EMG. Oxford University Press, 2013.

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36

Michell, Andrew. Understanding Emg. Oxford University Press, 2013.

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37

Pitt, Matthew. Motor unit anatomy and physiology. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198754596.003.0006.

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This chapter focuses on the signals recorded with needle electromyography (EMG) and the measurement of their specific parameters. These parameters include duration, amplitude, number of phases, and stability. The concept of the electrophysiologic biopsy and the explanation of unusual findings seen on EMG are introduced. In relation to the interference pattern, discussions of the firing rate, recruitment order, and interference pattern are given. Moving from the theoretical explanation of the findings, the problems of the accurate quantitative analysis of the motor unit potential are discussed
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38

Mills, Kerry R., ed. Oxford Textbook of Clinical Neurophysiology. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199688395.001.0001.

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The Oxford Textbook of Clinical Neurophysiology provides a comprehensive account from world experts of the modern practice of the specialty. It deals with the full range of techniques giving the underpinning basic science and clinical use. The importance of clinical skills, as well as technical expertise are emphasized. Section I reviews the physiology of nerve, muscle, and cortex, and the digital techniques used to study them. Section II discusses the techniques for nerve conduction, electromyography (EMG), electroencephalography (EEG), magnetoencephalography, evoked potentials, and transcran
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39

Pocket EMG. Springer Publishing Company, Incorporated, 2014.

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40

Shaibani, Aziz. Proximal Arm Weakness. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190661304.003.0012.

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Proximal arm muscles include supra and infra spinatii, pectoralis major and minor, teres major and minor, rhomboids, serratus anterior, deltoids, biceps, and triceps. The main function of these muscles is to abduct the arms. The first sign of proximal weakness is difficulty raising arms above the horizontal level. Shoulder conditions like supraspinatus tendonitis are often confused as proximal weakness. In myopathies, usually proximal arm weakness is associated with proximal leg weakness. Motor neuron diseases (MNDs) like amyotrophic lateral sclerosis (ALS) and spinal muscular atrophy (SMA) an
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41

Shaibani, Aziz. Myotonia. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190661304.003.0021.

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Myotonia is a slow relaxation phase after normal contraction. Patients report dystonia as muscle stiffness and sometimes pain. They usually adapt to it well. Falls due to myotonia may lead to accidents. Examination for percussion myotonia should be part of neuromuscular examination. Percussion of the thenar muscles with the reflex hammer is the most productive method. Electrically silent myotonia is a sign of Brody myopathy. Myotonia may be incidentally discovered during electromyography (EMG). The most important task is to differentiate between myotonia from paramyotonia clinically and electr
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42

Rubin, Devon I., and Jasper R. Daube. Clinical Neurophysiology. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190259631.001.0001.

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Clinical neurophysiologic testing is an important component of evaluating patients with complaints that may be attributed to diseases of the central or peripheral nervous system. This classic volume in the Contemporary Neurology Series covers the basic concepts underlying each of the testing techniques and provides comprehensive descriptions of the methods and wide range of electrophysiologic testing available for patients with epilepsy, neuromuscular diseases, movement disorders, demyelinating diseases, sleep disorders, autonomic disorders and those undergoing orthopedic and neurosurgical pro
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43

Tsao, Bryan E., and Mark A. Ferrante. EMG Lesion Localization and Characterization: A Case Studies Approach. Springer Publishing Company, Incorporated, 2019.

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44

Katirji, Bashar. Routine Clinical Electromyography. Edited by Bashar Katirji. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190603434.003.0002.

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Nerve conduction studies and needle EMG represent the two essential parts of the clinical EMG study. In almost all patients, both studies need to be completed before a final conclusion is made. This chapter outlines the basic concepts of nerve conduction studies including stimulations, recordings, variables and sources of errors. This is followed by detailed discussions of basic pathophysiological changes that accompany peripheral nerve disorders. The chapter then covers the normal needle EMG findings including normal insertional activity, motor unit action potential morphology and recruitment
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45

Geiringer, Steve R. Anatomic Localization for Needle EMG. 2nd ed. Hanley & Belfus, 1999.

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46

Brallier, Jess W., and Jonathan S. Gal. Neuroprotection for Spine Surgery. Edited by David L. Reich, Stephan Mayer, and Suzan Uysal. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190280253.003.0020.

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Perioperative neurologic injury related to spine surgery, albeit rare, can result in devastating functional loss. As the number of spine operations has increased, so has the need for strategies designed to avoid and protect against such injury. This chapter reviews the common etiologies of neurologic deficits secondary to spine surgery and the factors that place patients at increased risk for developing these complications. The use of intraoperative neuromonitoring, including somatosensory evoked potentials (SSEPs), electromyography (EMG), and transcranial motor evoked potentials (TcMEPs), to
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47

Luginbühl, Martin, and Arvi Yli-Hankala. Assessment of the components of anaesthesia. Edited by Antony R. Wilkes and Jonathan G. Hardman. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199642045.003.0026.

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In modern anaesthesia practice, hypnotic drugs, opioids, and neuromuscular blocking agents (NMBAs) are combined. The introduction of NMBAs in particular substantially increased the risk of awareness and recall during general anaesthesia. Hypnotic drugs such as propofol and volatile anaesthetics act through GABAA receptors and have typical effects on the electroencephalogram (EEG). During increasing concentrations of these pharmaceuticals, the EEG desynchronization is followed by gradual synchronization, slowing frequency, and increasing amplitude of EEG, thereafter EEG suppressions (burst supp
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48

Greenberg, Steven, and Anthony Amato. EMG Pearls. Hanley & Belfus, 2004.

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49

Maximum speed of forearm flexion practice effects upon surface EMG signal characteristics. 1985.

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50

The effect of short term EMG biofeedback on neck muscle relaxation for rotary pursuit performance. 1990.

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