Books on the topic 'Multiple sclerosis'

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1

Jürg, Kesselring, ed. Multiple sclerosis. Cambridge: Cambridge University Press, 1997.

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2

Kalb, Rosalind C. Multiple Sclerosis. New York: Demos Medical Publishing, 2009.

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3

Olek, Michael J., ed. Multiple Sclerosis. Totowa, NJ: Humana Press, 2005. http://dx.doi.org/10.1385/1592598552.

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4

JÜRG, ERNST W, and KENNETH. MULTIPLE SCLEROSIS. Edited by LUDWIG. Abingdon, UK: Taylor & Francis, 1988. http://dx.doi.org/10.4324/9780203212974.

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5

Abramovitz, Melissa. Multiple sclerosis. Detroit: Lucent Books, 2010.

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6

Weissert, Robert, ed. Multiple Sclerosis. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-2630-5.

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7

Kesselring, Jurg, Giancarlo Comi, and Alan J. Thompson, eds. Multiple Sclerosis. Cambridge: Cambridge University Press, 2009. http://dx.doi.org/10.1017/cbo9780511781698.

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8

Weiner, Howard L., and James M. Stankiewicz, eds. Multiple Sclerosis. Oxford, UK: Wiley-Blackwell, 2012. http://dx.doi.org/10.1002/9781119963714.

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9

De Souza, Lorraine H. Multiple Sclerosis. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-3107-8.

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10

Goodkin, Donald E., and Richard A. Rudick, eds. Multiple Sclerosis. London: Springer London, 1996. http://dx.doi.org/10.1007/978-1-4471-1271-6.

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11

McDonald, W. I., and Donald H. Silberberg. Multiple sclerosis. London: Butterworths, 1986.

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12

W, Paty Donald, and Ebers George C, eds. Multiple sclerosis. Philadelphia: F.A. Davis, 1998.

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13

G, Warren Kenneth, and World Health Organization, eds. Multiple sclerosis. Geneva: World Health Organization, 2001.

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14

National Institutes of Health (U.S.). Clinical Center., ed. Multiple sclerosis. Bethesda, Md: U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, Warren Grant Magnuson Clinical Center, 1990.

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15

Farris, Naff Clay, ed. Multiple sclerosis. Detroit: Greenhaven Press, 2009.

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16

Brill, Marlene Targ. Multiple sclerosis. Tarrytown, N.Y: Marshall Cavendish Benchmark, 2008.

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17

P, Antel Jack, ed. Multiple sclerosis. Philadelphia: Saunders, 1995.

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18

Rosner, Louis J. Multiple sclerosis. New York: Prentice Hall Press, 1987.

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19

Executive, NHS, ed. Multiple sclerosis. Oldham: HMSO, 1995.

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20

Blaylock, Russell L. Multiple sclerosis. Atlanta, Ga: Pritchett & Hull, 1988.

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21

Aaseng, Nathan. Multiple sclerosis. New York: Franklin Watts, 2000.

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22

National Institutes of Health (U.S.). Clinical Center., ed. Multiple sclerosis. Bethesda, Md: U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, Warren Grant Magnuson Clinical Center, 1990.

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23

Paul, O'Connor. Multiple sclerosis. Toronto: Key Porter Books, 1998.

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24

O'Brien, Bernie. Multiple sclerosis. London: Office of Health Economics, 1987.

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25

Gold, Susan Dudley. Multiple sclerosis. Parsippany, N.J: Crestwood House, 1997.

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26

Iezzoni, Lisa I. Multiple sclerosis. Santa Barbara, Calif: Greenwood Press, 2010.

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27

Schwarz, Shelley Peterman. Multiple Sclerosis. New York: Demos Medical Publishing, 2009.

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28

Rog, David. Multiple sclerosis. 2nd ed. London: Class Pub., 2010.

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29

Kalb, Rosalind C. Multiple Sclerosis. New York: Demos Medical Publishing, 2009.

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30

Kloos, Hugh. Treat Multiple Sclerosis : Multiple Sclerosis Management: Multiple Sclerosis Self-Care Guide. Independently Published, 2021.

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31

Lassmann, Hans, Georg Ebers, and Alastair Compston. Mcalpine's Multiple Sclerosis. Churchill Livingstone, 1998.

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32

Multiple Sclerosis. New York: Demos Medical Publishing, 2009.

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33

Bhargava, Pavan, and Peter A. Calabresi. Multiple Sclerosis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0087.

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Multiple sclerosis is a chronic demyelinating neurological disorder of the brain and spinal cord, with both inflammatory and degenerative components. Current treatment strategies utilize immunomodulatory and immunosuppressive agents to reduce the inflammatory disease activity and retard accumulation of disability. Future challenges for treatment include identifying agents that will promote remyelination and axonal protection to help impact progressive forms of multiple sclerosis. This chapter discusses currently available disease modifying therapies, agents currently in phase 2/3 trials, and future directions in the treatment of multiple sclerosis.
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34

Scolding, Neil, and Alastair Wilkins. Multiple Sclerosis. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780199603251.001.0001.

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35

Hancock, Laura M., Jared M. Bruce, and Sharon G. Lynch. Multiple Sclerosis. Edited by C. Steven Richards and Michael W. O'Hara. Oxford University Press, 2013. http://dx.doi.org/10.1093/oxfordhb/9780199797004.013.020.

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Multiple sclerosis (MS) is a chronic disease that affects the central nervous system and can cause a wide variety of both physical and cognitive deficits. Mood disturbances are common, with as many as 50% of patients receiving a diagnosis of major depression during their lifetime. The risk of suicide is high and leaving depression untreated is associated with a host of additional MS symptoms. Depression in MS presents clinicians with unique challenges, as it is often difficult to distinguish from common neurological symptoms. The authors discuss recommended screening tools and therapeutic methods that can assist the clinician in successfully identifying and treating depression in MS.
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36

Weir, Andrew. Multiple sclerosis. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0231.

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Multiple sclerosis is an idiopathic inflammatory disorder of the CNS. The characteristic pathological feature is the occurrence of ‘plaques’: well-defined areas of myelin loss, with relative axonal preservation.
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37

Bradl, Monika, and Hans Lassmann. Multiple Sclerosis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199794591.003.0061.

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This is a digitally enhanced text. Readers can also see the coverage of this topic area in the second edition of Neuroglia. The second edition of Neuroglia was first published digitally in Oxford Scholarship Online and the bibliographic details provided, if cited, will direct people to that version of the text. Readers can also see the coverage of this topic area in the ...
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38

Kaplan, Tamara B., and Marcelo Matiello. Multiple Sclerosis. Edited by Angela O’Neal. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190609917.003.0026.

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Multiple sclerosis (MS) often affects women of childbearing age. There are many issues to consider when counseling women about their disease and treatment during this time. The Pregnancy in Multiple Sclerosis (PRIMS) study, published in 1998, is the best large-scale prospective study published to date. Based on this trial, and those that followed, it is recognized that the rate of relapse in MS decreases during pregnancy, especially during the third trimester, but there is a significant increase in relapse rate in the first three months postpartum. If relapses do occur during pregnancy, women are often treated with methylprednisolone, but this is generally avoided in the first trimester. Disease-modifying therapies (DMTs) are usually discontinued during preconception, pregnancy, and while breast-feeding. DMTs are classified under different FDA pregnancy categories based on human and animal data. Breast-feeding may influence postpartum relapse rate, but the true effect continues to be debated.
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39

Robinson, Ian. Multiple Sclerosis. Routledge, 2005. http://dx.doi.org/10.4324/9780203977835.

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40

Multiple Sclerosis. Elsevier, 2016. http://dx.doi.org/10.1016/c2013-0-19153-2.

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41

McDonald, W. Ian. Multiple Sclerosis. Edited by Jürg Kesselring. Translated by Jane Smith. Cambridge University Press, 1996. http://dx.doi.org/10.1017/cbo9780511575051.

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42

Miller, Aaron E., and Teresa M. DeAngelis. Multiple Sclerosis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199732920.003.0001.

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Multiple sclerosis (MS), the most common cause of disability due to a neurological disease in young adults, can pose a challenging diagnosis. In this chapter, we summarize the typical symptomatology and the radiographic and paraclinical findings in MS. In addition, we briefly review candidate differential diagnostic entities, the current diagnostic criteria, and therapeutic options.
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43

Coles, Alasdair, and Alastair Compston. Multiple sclerosis. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199658602.003.0016.

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The papers in this chapter illustrate the picture that has emerged of multiple sclerosis as an inflammatory disorder of the central nervous system, caused by a complex interplay of multiple genetic susceptibility alleles and unknown environmental triggers. Multiple sclerosis is a disease in which there is first demyelination of nerves, followed by axonal degeneration. Demyelination is caused by inflammation, as shown by the synthesis of immunoglobulins within the CNS, and magnetic resonance imaging has shown that only the minority of inflammatory lesions cause symptoms. All of these discoveries were made in the twentieth century, which ended with the first demonstration that a treatment—interferon-beta—could influence the natural history of the disease.
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44

Pakenham, Kenneth I. Multiple Sclerosis. Oxford University Press, 2012. http://dx.doi.org/10.1093/oxfordhb/9780199733989.013.0012.

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45

Smith, Andrew, Carlos A. Perez, and Flavia Nelson. Multiple Sclerosis. Cambridge University Press, 2021.

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46

Multiple sclerosis. Bethesda, Md: U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, Warren Grant Magnuson Clinical Center, 1990.

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47

Multiple Sclerosis. Washington, D.C.: National Academies Press, 2001. http://dx.doi.org/10.17226/10031.

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48

Rumrill, P. Multiple Sclerosis. Ios Pr Inc, 2000.

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49

Robinson, Ian. Multiple Sclerosis. Taylor & Francis Group, 2005.

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50

J. Baloyannis, Stavros, ed. Multiple Sclerosis. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.78425.

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