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Titlebook: Atlas of Neuromuscular Diseases; A Practical Guidelin Eva L. Feldman,James W. Russell,Stefan Meng Book 2021Latest edition Springer Nature S

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Charcot Foot: Conservative Management,athy, and less prevalent conditions such as plexopathy and neuronopathy share pain as central aspect that often requires treatment. Diagnosis often requires only a careful clinical history, but this can be assisted by validated instruments to distinguish neuropathic from non-neuropathic causes (e.g.
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Challenges in fMRI and Its Limitationsormed by the union of a dorsal sensory root and a ventral motor root. Based on their location, the resulting nerve roots define the dermatomal and myotomal maps. Lesions of nerve roots are termed a radiculopathy. Radiculopathies are most commonly secondary to degenerative boney spine disease, partic
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Feroze B. Mohamed PhD,Scott H. Faro MDcal structures..The . descends in a loop-like structure and serves a large area of skin innervation and several motor nerves. The dorsal rami of C1–4 innervate the paraspinal muscles..The . is formed from spinal nerves C5–8. The three trunks bifurcate into anterior and posterior divisions. The trunk
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Andrew J. Saykin PsyD,Heather A. Wishart PhD etiologies, depending on the nerve involved. In addition to electrophysiology, imaging—particularly MRI and ultrasound—is proving increasingly useful in the timely and proper diagnosis and treatment of mononeuropathies. Cartoons of anatomy, clinical images, and MR and ultrasound are helpful to demo
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P. Turski,B. Mock,E. Baker,S. Terae,M. Bahnas to rely on an understanding of muscle electrophysiology, pathology, and genetics to differentiate between an ever-increasing number of complex disorders of muscle. There are several groups of muscle diseases that include genetic and autoimmune conditions, among others. Understanding the interface
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