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Books on the topic 'Motoer Neuron Disease'

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Author: Grafiati

Published: 4 June 2021

Last updated: 8 February 2022

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1

Talbot, Kevin. Motor neuron disease. Oxford: Oxford University Press, 2008.

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2

Talbot, Kevin. Motor neuron disease. Oxford: Oxford University Press, 2008.

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3

Leigh, P. N., and Michael Swash, eds. Motor Neuron Disease. London: Springer London, 1995. http://dx.doi.org/10.1007/978-1-4471-1871-8.

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4

David, Oliver. Motor neurone disease. 2nd ed. London: Royal College of General Practitioners, 1994.

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5

1948-, Hunter Maggie, ed. Motor neurone disease. London: Routledge, 1998.

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6

Orrell, Richard William. Genetics of motor neuron disease. Manchester: University of Manchester, 1996.

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7

Talbot, Kevin. Motor neuron disease: A practical manual. Oxford: Oxford University Press, 2010.

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8

Talbot, Kevin. Motor neuron disease: A practical manual. Oxford: Oxford University Press, 2010.

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9

Motor neuron disease: A practical manual. Oxford: Oxford University Press, 2010.

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10

Association, Motor Neurone Disease. Motor neurone disease resource file. Northampton: Motor Neurone Disease Association, 2000.

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11

Motor neuron diseases: Causes, classification, and treatments. Hauppauge, N.Y: Nova Science Publishers, 2011.

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12

Motor neurone diseases: Amyotrophic lateral sclerosis. London: Chapman & Hall, 1995.

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13

McGovern, Andy. Against the odds: Living with motor neurone disease. Dublin: Londubh Books, 2013.

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14

Mowat, Linda. As long as possible: An encounter with motor neurone disease. Oxford: Quince, 2000.

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15

Siddons, Adrian. The molecular pathology and molecular genetics of motor neurone disease. Manchester: University of Manchester, 1997.

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16

Motor Neuron Disease. Chapman & Hall, 1993.

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17

Williams, A. C. Motor Neuron Disease. Chapman & Hall, 1993.

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18

Rutherford, Kunel, and John L. R. Forsythe. Motor Neuron Disease. Saunders Ltd., 2002.

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19

Turner, Martin R. Motor neuron disease. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0232.

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Motor neuron disease (MND) is characterized by progressive muscular weakness due to simultaneous degeneration of lower and upper motor neurons (L/UMNs). Involvement of LMNs, arising from the anterior horns of the spinal cord and brainstem, leads to secondary wasting as a result of muscle denervation. Involvement of the UMNs of the motor cortex and corticospinal tract results in spasticity. In ~85% of cases, there is clear clinical involvement of both, and the condition is termed ‘amyotrophic lateral sclerosis’ (ALS; a term often used synonymously with MND). In ~13% of cases, there may be only LMN signs apparent, in which case the condition is termed ‘progressive muscular atrophy’, although such cases have a natural history that is to largely identical to that of ALS. In a very small group of patients (~2%), there are only UMN signs for at least the first 4 years, in which case the condition is termed ‘primary lateral sclerosis’; such cases have a uniformly slower progression. There is clinical, neuropathological, and genetic overlap between MND and some forms of frontotemporal dementia.

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20

Talbot, Kevin, Martin R. Turner, Rachael Marsden, and Rachel Botell. Motor Neuron Disease. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780199547364.001.1.

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Written and designed to provide comprehensive, easily accessible advice for all healthcare professionals involved in the care of patients with this challenging condition, this resource addresses the entire care pathway from presentation to diagnosis to symptom management and end of life issues.

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21

C, Williams A., ed. Motor neuron disease. London: New York, 1994.

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22

W, Kuncl Ralph, ed. Motor neuron disease. London: W.B. Saunders, 2002.

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23

Thakore, Nimish, and Erik P. Pioro. Types of Motor Neuron Diseases. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0022.

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Disorders of lower motor neurons (LMNs, or anterior horn cells) and upper motor neurons (UMNs), jointly termed motor neuron disorders (MNDs), are diverse and numerous. The prototypical MND, namely amyotrophic lateral sclerosis (ALS), a relentlessly progressive lethal disorder of adults, is the subject of another section and will not be discussed further here. Other MNDs include spinal muscular atrophy (SMA), of which there are four types: Kennedy’s disease, Brown-Violetto-Van Laere, and Fazio-Londe syndromes, lower motor neuron disorders as part of neurodegenerations and secondary motor neuron disease as part of malignancy, radiation and infection.

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24

Kaplan, Tamara, and Tracey Milligan. Motor Neuron Disease (DRAFT). Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190650261.003.0018.

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The video in this chapter explores motor neuron disease, including amytrophic lateral sclerosis (ALS) and spinal muscular atrophy (SMA). It discusses the signs of upper motor neuron (UMN) and lower motor neuron (LMN) pathology, as well as Kennedy disease.

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25

Eisen, Andrew. Motor neurone disease. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199658602.003.0009.

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In this chapter, the following ten key events in motor neurone disease, also known as amyotrophic lateral sclerosis (ALS), are considered: the first description of ALS by Cruveilhier; discovery of the first SOD1 mutation; use of the ALSFRS (functional rating scale) for determining therapeutic trial outcomes; the contentious issue of establishing the site of onset of ALS; clinical, pathological, and molecular evidence indicating that frontotemporal dementia and ALS are closely related; demonstration that ALS bears some resemblance to the transmissible spongiform encephalopathies; use of Riluzole as the approved therapy for ALS; the major inflammatory component of ALS; a Guamanian disorder that is biochemically and ultrastructurally similar to that of Alzheimer’s disease; and awareness that the true onset of ALS is unknown but certainly precedes clinical onset by years or decades.

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26

Motor Neurone Disease. Taylor & Francis Group, 2017.

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27

Hunter, Margaret. Motor Neurone Disease. Routledge, 2005. http://dx.doi.org/10.4324/9780203981023.

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28

Pamela J., M.d. Shaw (Editor) and Michael J. Strong (Editor), eds. Motor Neuron Disorders (Blue Books of Practical Neurology). Butterworth-Heinemann, 2003.

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29

Leigh, P. N. Motor Neuron Disease: Biology and Management. Springer-Verlag Telos, 1995.

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30

Nigel, Leigh P., and Swash Michael, eds. Motor neuron disease: Biology and management. London: Springer-Verlag, 1995.

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31

L, Mancini Raffaele, ed. Motor neuron disease research progress. New York: Nova Biomedical Books, 2008.

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32

Motor Neuron Disease in Adults. Oxford University Press, Incorporated, 2015.

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33

Strong, Michael J. Dementia and Motor Neuron Disease. Informa Healthcare, 2006.

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34

J, Strong Michael, ed. Dementia and motor neuron disease. Abingdon [England]: Informa UK Ltd., 2006.

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35

Strong, Michael, ed. Dementia and Motor Neuron Disease. CRC Press, 2006. http://dx.doi.org/10.1201/9780367800161.

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36

Strong, Michael, and Andrew Kertesz, eds. Dementia and Motor Neuron Disease. CRC Press, 2006. http://dx.doi.org/10.1201/b14376.

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37

Bromberg, Mark, ed. Motor Neuron Disease in Adults. Oxford University Press, 2014. http://dx.doi.org/10.1093/med/9780199783113.001.0001.

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38

(Editor), Jean-Philippe Loeffler, and Jose-Luis Gonzalez de Aguilar (Editor), eds. Amyotrophic Lateral Sclerosis: Beyond the Motor Neuron (Neuro-Degenerative Diseases). S Karger Pub, 2006.

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39

Leigh, P. Nigel. Motor Neuron Disease:: Biology and Management. Springer, 1995.

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40

Leigh, P. N. Motor Neuron Disease: Biology And Management. Springer, 2011.

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41

Motor Neuron Disease: Biology and Management. Springer, 2011.

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42

Foyaca Sibat, Humberto, and Lourdes de Fátima Ibañez-Valdés, eds. Novel Aspects on Motor Neuron Disease. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.73840.

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43

Association, Motor Neurone Disease, ed. Motor neurone disease information pack. [Northampton: Motor Neurone Disease Association, 1987.

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44

Clinical Neurophysiology of Motor Neuron Diseases. Elsevier, 2004. http://dx.doi.org/10.1016/s1567-4231(00)x0003-2.

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45

Motor neuron disorders and related diseases. Elsevier, 2007. http://dx.doi.org/10.1016/s0072-9752(07)x8001-1.

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46

1936-, Eisen Andrew, ed. Clinical neurophysiology of motor neuron diseases. Amsterdam: Elsevier, 2004.

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47

(Editor), Michael P. Barnes, and Garth R. Johnson (Editor), eds. Upper Motor Neurone Syndrome and Spasticity: Clinical Management and Neurophysiology. Cambridge University Press, 2001.

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48

1952-, Barnes Michael P., and Johnson Garth R. 1945-, eds. Upper motor neurone syndrome and spasticity: Clinical management and neurophysiology. New York, NY: Cambridge University Press, 2001.

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49

Cauchi, Ruben. Drosophila Melanogaster Models of Motor Neuron Disease. Nova Science Publishers, Incorporated, 2013.

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50

Soileau, Michael J., and Kelvin L. Chou. Parkinson Disease. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0002.

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Parkinson disease is a neurodegenerative disorder characterized clinically by tremor, rigidity, bradykinesia, and postural instability and pathologically by loss of nigrostriatal neurons and deposition of alpha-synuclein in neuronal cell bodies and neuritis. Non-motor symptoms such as psychiatric disorders, cognitive abnormalities, sleep dysfunction, autonomic dysfunction, and sensory manifestations are also common. This chapter gives a broad overview of this disorder. Sections cover pathophysiology, genetics, clinical manifestations, and disease course. The chapter also briefly discusses how to make the diagnosis, and alternative conditions that should be considered.

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