Books on the topic 'Amyotrophic lateral sclerosis – Research'

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1

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

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2

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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3

Eisen, Andrew. Amythrophic lateral sclerosis: A synthesis of research and clinical practice. Cambridge: Cambridge University Press, 1998.

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4

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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5

Gajdusek, D. Carleton. Interference with axonal transport of neurofilament as the common etiology and pathogenesis of neurofibrillary tangles, amyotrophic lateral sclerosis, parkinsonism-dementia, and many other degenerations of the CNS: A series of hypotheses, perspectives for research. Bethesda, Md: U.S. Dept. of Health and Human Services, National Institutes of Health, Laboratory of Central Nervous System Studies, National Institute of Neurological and Communicative Disorders and Stroke, 1985.

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6

Imaharu, Nakano, and Hirano Asao 1926-, eds. Amyotrophic lateral sclerosis: Progress and perspectives in basic research and clinical application : proceedings of the 11th Tokyo Metropolitan Institute for Neuroscience (TMIN) International Symposium, Tokyo, October 25-27, 1995. Amsterdam: Elsevier Science, 1996.

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7

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

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8

Research, Institute for Career. Careers in medical research: Finding cures for paralysis : spinal cord injuries, stroke, multiple sclerosis, cerebral palsy, amyotrophic lateral sclerosis : unlocking the mysteries of the brain and fixing a broken body. [Chicago, Ill.]: Institute for Career Research, 2003.

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9

Parker, Philip M., and James N. Parker. Sclerosis: A medical dictionary, bibliography, and annotated research guide to Internet references. San Diego, CA: ICON Health Publications, 2003.

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10

United, States Congress Senate Committee on Appropriations Subcommittee on Departments of Labor Health and Human Services Education and Related Agencies. Amyotrophic lateral sclerosis (ALS): Hearing before a subcommittee of the Committee on Appropriations, United States Senate, One Hundred Ninth Congress, first session, special hearing, May 11, 2005, Washington, DC. Washington: U.S. G.P.O., 2006.

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11

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

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12

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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13

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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14

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

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15

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

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16

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

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17

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

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18

Behind those eyes: Our journey with ALS. Renfrew, Ont: General Store Publishing House, 2013.

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19

Respiratory management of ALS: Amyotrophic lateral sclerosis. Sudbury, Mass: Jones and Bartlett, 2009.

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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

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

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22

Six parts love: One family's battle with Lou Gehrig's disease. New York: Scribner, 1985.

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23

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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24

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

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25

Amyotrophic Lateral Sclerosis: Current Research. Murphy & Moore Publishing, 2022.

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26

Murray, Christine A. Amyotrophic Lateral Sclerosis: New Research. Nova Biomedical Books, 2004.

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27

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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28

Amyotrophic Lateral Sclerosis:Therapeutic, Psychological and Research Aspects. Springer, 1987.

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29

Nicholson, Katharine A., and James D. Berry. Amyotrophic Lateral Sclerosis Clinical Trials. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0030.

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The current state of amyotrophic lateral sclerosis (ALS) trial design is best understood within the context of ALS research over the past quarter century. Before the early 1990s, trials in ALS were typically small and clinical trial methodology was less rigorous than it is today. With the discovery of the SOD1 gene mutation in the early 1990s, a new era of excitement and innovation for ALS research began. Since then, the number of ALS trials has steadily increased and trial design and methodology has become increasingly sophisticated.
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30

Amyotrophic Lateral Sclerosis: A Synthesis of Research and Clinical Practice. Cambridge University Press, 2006.

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31

Cosi, V. Amyotrophic Lateral Sclerosis: Therapeutic, Psychological, and Research Aspects. Springer, 2012.

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32

Cosi, V. Amyotrophic Lateral Sclerosis: Therapeutic, Psychological, and Research Aspects. Springer London, Limited, 2013.

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33

Krieger, Charles, and Andrew Eisen. Amyotrophic Lateral Sclerosis: A Synthesis of Research and Clinical Practice. Cambridge University Press, 2011.

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34

Krieger, Charles, and Andrew Eisen. Amyotrophic Lateral Sclerosis: A Synthesis of Research and Clinical Practice. Cambridge University Press, 1998.

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35

Krieger, Charles, and Andrew Eisen. Amyotrophic Lateral Sclerosis: A Synthesis of Research and Clinical Practice. Cambridge University Press, 2010.

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36

Watermeyer, Tamlyn J., and Laura H. Goldstein. Psychological research in amyotrophic lateral sclerosis: Past, present, and future. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198757726.003.0001.

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This chapter, of particular interest to those interested in psychological treatments for people with amyotrophic lateral sclerosis (ALS), outlines earlier work that sought to identify correlates of reduced well-being and quality of life in people with ALS and delineates possible targets for intervention. In this context, the chapter then evaluates several studies that have investigated psychological interventions for optimizing well-being in people with ALS and their caregivers. The chapter reviews current efforts to address the paucity of interventional research in this patient group, focusing on five therapies that have so far been evaluated for treatment efficacy. These therapies include hypnosis, mindfulness, cognitive behavioural therapy, expressive disclosure therapy, and dignity therapy. The main findings from these studies and their clinical implications for people with ALS and their families are discussed. Recommendations for future research are considered, together with a discussion of the implementation of such interventions in therapeutic or multidisciplinary settings.
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37

China) International Conference on Advances in Structural Dynamics (2000 : Hong Kong and Tadao Tsubaki. Amyotrophic Lateral Sclerosis: Recent Advances in Research and Treatment : Proceedings of the International Conference on Amyotrophic Lateral Sclero (International Congress Series). Excerpta Medica, 1988.

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38

Rouzic, Jean-Pierre Le. Status of Amyotrophic Lateral Sclerosis Research: From Stopping the Disease to Restoring the Motor Function. Independently Published, 2019.

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39

Devi, Gourie M. Motor Neurone Disease: Global Clinical Patterns and International Research. South Asia Books, 1987.

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40

M, Gourie-Devi, Indian Council of Medical Research., NIMHANS (Institute), and International Symposium on Motor Neurone Disease (1984 : Bangalore, India), eds. Motor neurone disease: Global clinical patterns and international research. New Delhi: Oxford & IBH Pub. Co., 1987.

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41

Calne, Donald, ed. Advances In Research On Neurodegeneration Vol.1: DEFINITIONS, CLINICAL FEATURES, AND MORPHOLOGY (ADVANCES IN RESEARCH ON NEURODEGENERATION). Birkhauser Boston, 1993.

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42

Amyotrophic Lateral Sclerosis (ALS): Hearing Before a Subcommittee of the Committee on Appropriations, United States Senate, One Hundred Ninth Congres. Not Avail, 2006.

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43

Katirji, Bashar. Case 19. Edited by Bashar Katirji. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190603434.003.0023.

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Amyotrophic lateral sclerosis is a fatal neurological disorder, classically presenting with signs of upper motor neuron and lower motor neuron degeneration. Several motor neuron disease variants with purely upper or lower motor neuron degeneration exist. These includes primary lateral sclerosis, progressive muscular atrophy and progressive bulbar palsy. The diagnostic criteria, including El-Escorial criteria and its most recent Awaji revision, are not used in clinical practice and for research purposes. This case highlights the clinical features and electrodiagnostic characteristics of amyotrophic lateral sclerosis. The findings on nerve conduction studies and needle electromyography are emphasized in detail. The role of electrodiagnostic studies in the diagnosis of amyotrophic lateral sclerosis is to establish evidence of lower motor neuron degeneration, confirm its diffuse nature, and exclude treatable causes (such as multifocal motor neuropathy and mimickers of motor neuron disease such as chronic myopathies).
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44

Lou Gehrig's Disease - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References. ICON Health Publications, 2004.

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45

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

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46

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

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47

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

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48

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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49

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

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50

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

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