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1

Mark, Hallett, and Millender Lewis H. 1937-, eds. Entrapment neuropathies. 2nd ed. Boston: Little, Brown, 1990.

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2

Asbury, Arthur K., Herbert Budka, and Elfriede Sluga, eds. Sensory Neuropathies. Vienna: Springer Vienna, 1995. http://dx.doi.org/10.1007/978-3-7091-6595-9.

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3

R, Oppenheimer D., and Esiri Margaret M, eds. Oppenheimer's diagnostic neuropathology: A practical manual. 2nd ed. Oxford: Blackwell Science, 1996.

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4

Kuhlenbäumer, Gregor, Florian Stögbauer, E. Bernd Ringelstein, and Peter Young. Hereditary Peripheral Neuropathies. Darmstadt: Steinkopff, 2005. http://dx.doi.org/10.1007/3-7985-1586-7.

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5

Penkert, Götz, Josef Böhm, and Thomas Schelle. Focal Peripheral Neuropathies. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-54780-5.

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6

Focal peripheral neuropathies. 2nd ed. New York: Raven Press, 1993.

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7

Hayreh, Sohan Singh. Ischemic Optic Neuropathies. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11852-4.

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8

Hayreh, Sohan Singh. Ischemic optic neuropathies. Heidelberg: Springer, 2011.

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9

Focal peripheral neuropathies. New York: Elsevier, 1987.

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10

Stephen, Scelsa, and Schaumburg Herbert H. 1932-, eds. Peripheral neuropathies in clinical practice. New York: Oxford University Press, 2010.

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11

Sotereanos, Dean G., and Loukia K. Papatheodorou, eds. Compressive Neuropathies of the Upper Extremity. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-37289-7.

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12

Pfeifer, Michael A. Diabetic neuropathy. Kalamazoo, Mich: Upjohn, 1985.

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13

International Symposium on Peripheral Neuropathies (1987 Geneva, Switzerland). Peripheral neuropathies 1988: What is significantly new? Padova: Liviana Press, 1989.

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14

Duncan, Scott F. M., and Ryosuke Kakinoki, eds. Carpal Tunnel Syndrome and Related Median Neuropathies. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-57010-5.

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15

International, Symposium on Diabetic Neuropathy (3rd 1994 Kanagawa-ken Japan). Diabetic neuropathy: New concepts and insights : proceedings of the 3rd International Symposium on Diabetic Neuropathy, Kanagawa, 3-5 November 1994. Amsterdam: Elsevier, 1995.

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16

Grateau, Gilles. Les amyloses. Paris: Médecine-Sciences Flammarion, 2000.

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17

Loretta, Vileikyte, ed. Painful diabetic neuropathy in clinical practice. London: Springer, 2011.

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18

Darvill, Angela Marie. Investigation of the autoimmune component of IGA related neuropathies. Manchester: University of Manchester, 1993.

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19

Kaga, Kimitaka, and Arnold Starr, eds. Neuropathies of the Auditory and Vestibular Eighth Cranial Nerves. Tokyo: Springer Japan, 2009. http://dx.doi.org/10.1007/978-4-431-09433-3.

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20

Veves, Aristidis. Diabetic neuropathy: Clinical management. 2nd ed. Totowa, N.J: Humana Press, 2007.

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21

Veves, Aristidis. Diabetic neuropathy: Clinical management. 2nd ed. Totowa, N.J: Humana Press, 2007.

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22

Veves, Aristidis. Diabetic neuropathy: Clinical management. 2nd ed. Totowa, N.J: Humana Press, 2007.

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23

Veves, Aristidis. Diabetic neuropathy: Clinical management. 2nd ed. Totowa, N.J: Humana Press, 2007.

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24

Antia, Noshir H. The surgical management of deformities in leprosy and other peripheral neuropathies. Bombay: Oxford University Press, 1992.

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25

Prikhozhan, V. M. Neurological disturbances in diabetes mellitus. 2nd ed. Eastbourne: Praeger, 1985.

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26

Numb toes and other woes: More on peripheral neuropathy. San Antonio, Tx: MedPress, 2001.

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27

Aldea, Juan Jose Poza. Neuropatias Diabeticas Dolorosas. Ars Medica, 2006.

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28

1927-, Vinken P. J., Bruyn G. W. 1928-, Klawans Harold L. 1937-, and Matthews W. B, eds. Neuropathies. Amsterdam: Elsevier Science, 1987.

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29

J, Vinken P., and Matthews W. B, eds. Neuropathies. Amsterdam: Elsevier Science Publishers, 1987.

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30

1928-, Asbury Arthur K., Budka H, and Sluga Elfriede 1930-, eds. Sensory neuropathies. Wien: Springer-Verlag, 1995.

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31

Rajabally, Yusuf. Inflammatory Neuropathies. Elsevier Science & Technology, 2020.

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32

Hartung, H. P. Peripheral Neuropathies. Elsevier, 1996.

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33

Rajabally, Yusuf. Dysimmune Neuropathies. Elsevier Science & Technology Books, 2020.

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34

Low, Phillip A. Autonomic Neuropathies. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0118.

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Autonomic neuropathy is a peripheral neuropathy with selective or disproportionate involvement of autonomic fibers. Because autonomic nerves innervate all organ systems, the manifestations of dysautonomia are protean. There are many causes of the autonomic neuropathies (Table 118.1). Some of the disorders in Table 118.1 are described in detail in other chapters. This chapter provides a brief description of the autonomic neuropathies, going from the acute/subacute to the more slowly evolving categories and finishing with some entities with less generalized dysautonomia.
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35

Teener, James W. Entrapment Neuropathies. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0122.

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Entrapment neuropathies are a subset of compression neuropathies caused by chronic impingement upon a nerve by nearby structures. The resulting pathology depends upon the duration and severity of entrapment, and ranges from demyelination if entrapment is mild or brief to axonal loss in more severe cases. Entrapment neuropathies typically cause symptoms referable to a single nerve distribution, but sensory symptoms may appear to extend beyond the typical dermatome of the entrapped nerve. Diagnosis is based upon clinical history and examination, and is supported by electrodiagnostic studies and imaging. A variety of supportive therapies may result in improvement of symptoms, but in cases of severe entrapment, surgical intervention to release the nerve is often necessary, and even then recovery is often incomplete.
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36

Goodfellow, John A., Amy I. Davidson, and Hugh J. Willison. Demyelinating Neuropathies. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0123.

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Many neuropathies have in common the basic pathophysiological mechanism of demyelination. Our understanding of the normal process of myelination and the molecular structure of myelin, nodes of Ranvier, and internodes has increased in recent years, yielding a greater understanding of the process of demyelination in disease. This chapter focuses on the inherited neuropathies as examples of non-inflammatory demyelinating neuropathies. For these conditions there are ongoing genotype-phenotype correlations and a greater appreciation of the importance of distal axonal degeneration as a consequence of demyelination.
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37

Bland, Jeremy D. P. Focal neuropathies. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199688395.003.0019.

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Focal neuropathies discusses the clinical, neurophysiological, and imaging assessment of the group of localized nerve lesions which are often referred to as ‘tunnel syndromes’. It first sets out general principles about how to define these syndromes and for their clinical, neurophysiological, and imaging assessment. Secondly, it discusses the relative importance of neurophysiological testing in diagnosis, prognosis, and the detection of coincident pathology when assessing these disorders. Finally, it then applies these principles to the example conditions of carpal tunnel syndrome, ulnar neuropathy at the elbow, peroneal neuropathy at the knee, and tarsal tunnel syndrome, and illustrates the use of neurophysiological tests as part of a comprehensive assessment intended to guide patient management.
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38

Misulis, Karl E., and E. Lee Murray. Cranial Neuropathies. Edited by Karl E. Misulis and E. Lee Murray. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190259419.003.0008.

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Single cranial neuropathies are much more common than multiple cranial neuropathies but both are discussed in this chapter. The most common single cranial neuropathies are facial, abducens, oculomotor, and optic. Multiple cranial neuropathies can develop for a variety of reasons, but among the most common are neoplastic meningitis, vasculitis, diabetes, and intrinsic brainstem lesions.
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39

Dysimmune Neuropathies. Elsevier, 2020. http://dx.doi.org/10.1016/c2017-0-01282-x.

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40

-P, Hartung H., ed. Peripheral neuropathies. London: Baillière Tindall, 1996.

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41

1930-, Dawson D. M., Hallett Mark, Wilbourn Asa J, Campbell William W, Terrono Andrew L, and Trepman Elly, eds. Entrapment neuropathies. 3rd ed. Philadelphia: Lippincott Raven, 1999.

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42

Young, P., E. B. Ringelstein, G. Kuhlenbäumer, and F. Stögbauer. Hereditary Peripheral Neuropathies. Kuhlenbaumer G, 2014.

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43

Peripheral Neuropathies 1988. Springer Verlag, 1990.

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44

Hayreh, Sohan Singh. Ischemic Optic Neuropathies. Springer, 2014.

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45

(Editor), G. Kuhlenbäumer, F. Stögbauer (Editor), E. B. Ringelstein (Editor), and P. Young (Editor), eds. Hereditary Peripheral Neuropathies. Steinkopff-Verlag Darmstadt, 2005.

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46

Hereditary Peripheral Neuropathies. Steinkopff, 2006.

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47

Stewart, John D. Focal Peripheral Neuropathies. 3rd ed. Lippincott Williams & Wilkins, 2000.

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48

Davidson, Amy I., John A. Goodfellow, and Hugh J. Willison. Immune-Mediated Neuropathies. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0124.

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Immune-mediated neuropathies are a spectrum of diverse conditions with a commonality springing from dysregulation of the immune system. Clinical phenotypes can vary, along with onset and evolution of the condition, though paresis, paraesthesia, and pain are all common hallmarks. These conditions, although relatively rare, can be potentially life threatening, and functionally debilitating. The mainstay of treatment is immunomodulation, which continues to be an area of research interest, and with our improving understanding of the neurobiology of these conditions, novel targets are arising. This chapter looks to define these clinical syndromes, shedding light on their underpinning mechanisms and how to manage them.
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49

Franssen, Hessel. Generalized peripheral neuropathies. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199688395.003.0020.

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The chapter on generalized peripheral neuropathies describes how to perform and interpret electrophysiological studies aimed at diagnosing polyneuropathy. It first reviews methodological issues, such as stimulation and recording, and takes into account temperature. Next, the relevant pathophysiology of single myelinated axons, as found in animal experiments, is discussed and related to findings on nerve conduction studies performed in patients. This is followed by a discussion of criteria for axon loss and demyelination. Finally, typical findings in specific neuropathies are described and examples of typical findings are shown in the figures.
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50

Tratado de dolor neuropatico. Editorial Médica Panamericana, 2006.

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