Books on the topic 'Amyotrophic lateral sclerosis'

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1

Brown, Robert H., Michael Swash, and Piera Pasinelli. Amyotrophic Lateral Sclerosis. 2nd ed. London: CRC Press, 2021. http://dx.doi.org/10.1201/9781003076445.

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2

Cosi, V., Ann C. Kato, W. Parlette, P. Pinelli, and M. Poloni, eds. Amyotrophic Lateral Sclerosis. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4684-5302-7.

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3

MD, Brown Robert H., Swash Michael, and Pasinelli Piera, eds. Amyotrophic lateral sclerosis. 2nd ed. Abingdon [England]: Informa Healthcare, 2006.

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4

1947-, Brown Robert H., Meininger Vincent, and Swash Michael, eds. Amyotrophic lateral sclerosis. London: Martin Dunitz, 2000.

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5

National Institute of Neurological Disorders and Stroke (U.S.). Office of Communications and Public Liaison, ed. Amyotrophic lateral sclerosis. Bethesda, Md: U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, 2000.

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6

1949-, Chad David A., and Pioro Erik P. 1955-, eds. Amyotrophic lateral sclerosis. Philadelphia: F.A. Davis, 1998.

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7

Clifford, Rose F., ed. Amyotrophic lateral sclerosis. New York, N.Y: Demos, 1990.

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8

1952-, Brown Robert H., Meininger Vincent, and Swash Michael, eds. Amyotrophic lateral sclerosis. London: Martin Dunitz, 2000.

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9

Hiroshi, Mitsumoto, Przedborski Serge, and Gordon Paul H, eds. Amyotrophic lateral sclerosis. Boca Raton: Taylor & Francis, 2006.

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10

A, Murray Christine, ed. Amyotrophic lateral sclerosis: New research. New York: Nova Biomedical Books, 2006.

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11

Ludwig, Gutmann, and Mitsumoto Hiroshi, eds. Advances in amyotrophic lateral sclerosis. Boston, Mass: Little, Brown, 1996.

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12

G, Farrell Jason, ed. New amyotrophic lateral sclerosis research. New York: Nova Biomedical Books, 2008.

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13

1941-, Smith Richard Alan, ed. Handbook of amyotrophic lateral sclerosis. New York: Dekker, 1992.

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14

Hiroshi, Mitsumoto, ed. Amyotrophic lateral sclerosis: A guide for patients and families. 3rd ed. New York, NY: Demos Health, 2009.

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15

National Institute of Neurological Disorders and Stroke (U.S.). Office of Communications and Public Liaison. ALS (Amyotrophic lateral sclerosis) fact sheet. Bethesda, MD: National Institutes of Health, 2010.

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16

Perez-Torres, Eduardo J. Retromer deficiency in amyotrophic lateral sclerosis. [New York, N.Y.?]: [publisher not identified], 2020.

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17

1921-, Tsubaki Tadao, and Yase Yoshirō, eds. Amyotrophic lateral sclerosis: Recent advances in research and treatment : proceedings of the International Conference on Amyotrophic Lateral Sclerosis, Kyoto, Japan, 29-31, October 1987. Amsterdam: Excerpta Medica, 1988.

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18

Serratrice, Georges. Pathogenesis and therapy of amyotrophic lateral sclerosis. Philadelphia: Lippincott-Raven, 1995.

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19

T, Serratrice Georges, and Munsat Theodore L, eds. Pathogenesis and therapy of amyotrophic lateral sclerosis. Philadelphia: Lippincott-Raven, 1995.

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20

Guion, Lee. Respiratory management of ALS: Amyotrophic lateral sclerosis. Sudbury, Mass: Jones and Bartlett, 2010.

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21

M, Belsh Jerry, and Schiffman Philip L, eds. Amyotrophic lateral sclerosis: Diagnosis and management for the clinician. Armonk, NY: Futura, 1996.

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22

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

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23

1924-, Hudson Arthur J., and Canadian Congress of Neurological Sciences (22nd : 1987 : Vancouver, B.C.), eds. Amyotrophic lateral sclerosis: Concepts in pathogenesis and etiology. Toronto: University of Toronto Press, 1990.

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24

Scott, Donald W. (Donald William) 1924. Amyotrophic lateral sclerosis: The probable cause, a possible cure. Victoria, B.C: Trafford, 2002.

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25

International, Congress on Therapeutic Psychological and Research Aspects of Amyotrophic Lateral Sclerosis (1985 Varese Italy). Amyotrophic lateral sclerosis: Therapeutic, psychological, and research aspects. New York, N.Y: Plenum Press, 1987.

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26

Hiroshi, Mitsumoto, and Norris Forbes H. 1928-, eds. Amyotrophic lateral sclerosis: A comprehensive guide to management. New York, NY: Demos, 1994.

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27

T, Caroscio James, ed. Amyotrophic lateral sclerosis: A guide to patient care. New York: Thieme, 1986.

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28

1942-, Miller Robert G., ed. Amyotrophic lateral sclerosis standard of care consensus conference. Hagerstown, MD: Lippincott-Raven, 1997.

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29

Parker, James N., and Philip M. Parker. The official patient's sourcebook on amyotrophic lateral sclerosis. Edited by Icon Group International Inc. San Diego, Calif: Icon Health Publications, 2003.

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30

P, Rowland Lewis, and Muscular Dystrophy Association, eds. Amyotrophic lateral sclerosis and other motor neuron diseases. New York: Raven Press, 1991.

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31

Swash, Michael, Robert Brown, and Piera Pasinelli. Amyotrophic Lateral Sclerosis. Taylor & Francis Group, 2005.

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32

Jr., Robert H. Brown (Editor), Michael Swash (Editor), and Piera Pasinelli (Editor), eds. Amyotrophic Lateral Sclerosis, Second Edition. 2nd ed. Informa Healthcare, 2006.

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33

Hayertz, Marchelle. Amyotrophic Lateral Sclerosis Treatment : Amyotrophic Lateral Sclerosis Treatment and Management: Amyotrophic Lateral Sclerosis Pronunciation. Independently Published, 2021.

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34

Mitsumoto, Hiroshi, Serge Przedborski, and Paul H. Gordon. Amyotrophic Lateral Sclerosis. Taylor & Francis Group, 2005.

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35

Pagnini, Francesco, and Zachary Simmons, eds. Amyotrophic Lateral Sclerosis. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198757726.001.0001.

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Amyotrophic lateral sclerosis: Understanding and optimizing quality of life and psychological well-being presents a comprehensive and up-to-date review of the enhancement of the lives of people with amyotrophic lateral sclerosis (ALS) and their caregivers. ALS is a progressive, fatal neurodegenerative disorder. No current medical therapy can reverse or stop its progression, and the promotion of quality of life and psychological well-being is a central component of ALS care. Health care professionals who work in this field should incorporate attention to psychological, emotional, and relational aspects of the disease into their approach to care. This book provides some of the knowledge and direction necessary for optimizing the quality of care for individuals with ALS and their caregivers. Topics discussed include an ALS-centred view of quality of life, depressive features, anxiety, resilience, cognitive impairment, complementary and alternative medicines, and psychological research. Specific elements of ALS, such as end-of-life concerns and bulbar dysfunction, are described through the lens of their psychological impact. There is extensive discussion of the development of new psychological treatments, as well as the impact and incorporation of new technologies, with the goal of fostering optimal quality of life and psychological well-being as key parts of a holistic approach to care for the patients and for those who are close to such individuals.
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36

Ferraiuolo, Laura, and Stephen J. Kolb. Amyotrophic Lateral Sclerosis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0026.

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An overriding mystery of ALS pathogenesis orbits around the molecular basis of selective motor neuron vulnerability and clouds our view. There are likely mechanisms involved in the initiation of motor neuron loss and mechanisms involved in the progression of motor neuron loss once initiated. Motor neuron vulnerability is likely related to the unique biological characteristics of these cells. This chapter introduces central molecular pathways that appear to be involved in the pathogenesis of ALS, and highlights why dysregulation of these mechanisms could lead to motor neuron death. Indeed, there are likely mechanisms involved in the initiation of motor neuron loss and mechanisms involved in the progression of motor neuron loss once initiated. Our task is to determine those mechanisms that are relevant to ALS pathogenesis that may be targeted therapeutically to prevent onset and/or halt progression.
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37

Harms, Matthew B., and Timothy M. Miller. Amyotrophic Lateral Sclerosis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0027.

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Recent advances in sequencing technologies have dramatically expanded the number of genes associated with amyotrophic lateral sclerosis, including rare but highly penetrant causative mutations as well as common risk alleles. This chapter discusses these gene discoveries and how they have implicated a diverse array of biological pathways essential for motor neuron health and have begun to inform our understanding of ALS pathogenesis as a heterogeneous and multistep process. Insights from these discoveries are leading to a new generation of targeted therapies directed at specific genes and are poised to inform how patients with amyotrophic lateral sclerosis are evaluated and treated in the clinic.
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38

Wainger, Brian J. Amyotrophic Lateral Sclerosis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0028.

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Mouse and cellular models of ALS including stem cells have revealed tremendous insight into the molecular processes that lead to ALS. Models of ALS and other neurodegenerative diseases have led to emergent molecular themes that span several diseases. Future models must account for neuronal subtype specificity of different neurodegenerative diseases, particularly between tightly related diseases such as FTD and ALS. Human iPSC-derived motor neurons offer promise both with regard to the use of human cells and in particular the ability to model sporadic disease, which is critically important given the overwhelming abundance of sporadic disease in ALS and other neurodegenerative diseases.
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39

Harris, Brent T., Galam A. Khan, and Saed Sadeghi. Amyotrophic Lateral Sclerosis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0029.

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Although the basic gross and microscopic pathological changes in amyotrophic lateral sclerosis (ALS) have been known for more than 100 years, emerging technology and research into the cellular and molecular changes found in this disease are challenging our understanding about the pathogenesis and pathophysiology. All cell types of the CNS/PNS as well as circulating immune cells have been implicated in the pathology of ALS. Numerous genes, their proteins, and environmental factors have also been associated. However, we still do not understand the specific gene-environmental interactions that bring about and drive this devastating disease in most cases. This short chapter does not address the causal factors and molecular pathogeneses that have been hypothesized and actively researched in the pathology of ALS-as these are discussed in other sections of this text. Here, it shows and discusses the basic pathological changes at the tissue and cellular levels that help to establish the pathological diagnosis of ALS at autopsy.
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40

Mitsumoto, Hiroshi, Serge Przedborski, and Paul H. Gordon, eds. Amyotrophic Lateral Sclerosis. CRC Press, 2005. http://dx.doi.org/10.1201/b14133.

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41

Sattler, Rita, and Jeffrey Rothstein. Amyotrophic Lateral Sclerosis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199794591.003.0063.

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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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42

Araki, Toshiyuki, ed. Amyotrophic Lateral Sclerosis. Exon Publications, 2021. http://dx.doi.org/10.36255/exonpublications.amyotrophiclateralsclerosis.2021.

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43

Maurer, Martin, ed. Amyotrophic Lateral Sclerosis. InTech, 2012. http://dx.doi.org/10.5772/1054.

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44

Amyotrophic Lateral Sclerosis. ReadHowYouWant.com, Limited, 2010.

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45

Swash, Michael, Robert Brown, and Piera Pasinelli. Amyotrophic Lateral Sclerosis. Taylor & Francis Group, 2006.

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46

Mitsumoto, Hiroshi, Serge Przedborski, and Paul H. Gordon. Amyotrophic Lateral Sclerosis. Taylor & Francis Group, 2019.

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47

Gelinas, Deborah, and Miller Robert. Amyotrophic Lateral Sclerosis. Springer Publishing Company, Incorporated, 2010.

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48

Estevez, Alvaro G., Jin Hee Shin, and Fabian H. Rossi. Amyotrophic Lateral Sclerosis. DI Press, 2022.

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49

Brown, Jr Robert H., Vincent Meininger, and Michael Swash. Amyotrophic Lateral Sclerosis. 2nd ed. Informa Healthcare, 2000.

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50

Gelinas, Deborah, Patricia O'Connor, and Robert G. Miller. Amyotrophic Lateral Sclerosis. Springer Publishing Company, Incorporated, 2005.

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