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Books on the topic 'Amyotrophic lateral sclerosis, ALS'

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Author: Grafiati
Published: 4 June 2021
Last updated: 7 July 2024

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1

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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2

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

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3

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

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4

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

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5

Amyotrophic Lateral Sclerosis Society of Canada., ed. Resources for ALS healthcare providers. Toronto: The Society, 1994.

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6

ALS: Lou Gehrig's disease: Patient advocate. Riverside, CA: Health Scouter - Equity Press, 2009.

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7

Koka, Halil. Bana ALS teşhisi koydular: Bir ALS hastasının umut dolu savaşı. İstanbul: Cinius, 2010.

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8

Stinton, William M. I choose to live: A journey through life with ALS. Gurnee, IL: Banbury Pub., 2003.

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9

I choose to live: A journey through life with ALS. Gurnee, IL: Banbury Pub., 2003.

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10

Stinton, William M. I choose to live: A journey through life with ALS. Gurnee, IL: Banbury Pub., 2003.

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11

Jun, Kimura, and Kaji Ryuji, eds. Physiology of ALS and related diseases. Amsterdam: Elsevier, 1997.

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12

author, Silverman Jennifer, and Holt Kim illustrator, eds. My dad has ALS? Place of publication not identified]: [Bookbaby], 2015.

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13

Radin, Yaakov. "Friends 4 ALS" concert. [Brooklyn, NY]: MRM Music, 2012.

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14

ALS Registry Act: Report (to accompany H.R. 2295) (including cost estimate of the Congressional Budget Office). [Washington, D.C: U.S. G.P.O., 2007.

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15

Columbia University. Department of Neurology. Recent advances in ALS and other neuromuscular diseases: Featuring the 2nd annual Eleanor & Lou Gehrig lecture, Friday June 21, 1996. [New York?]: Columbia University, 1996.

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16

Massachusetts. Bureau of Environmental Health. Environmental Epidemiology Program. The Amyotrophic Lateral Sclerosis (ALS) Disease Registry: Frequently asked questions for patients and families. Boston, Mass.]: Massachusetts Department of Public Health, Bureau of Environmental Health, Environmental Epidemiology Program, 2009.

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17

Kaye, Dennis. Laugh, I thought I'd die: My life with ALS. Toronto: Penguin, 1993.

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18

DeGraff, Rosemary. Twilight of a dancer: The story of Katherine Collingwood and her heroic battle with ALS. Winnipeg: Peguis Publishers, 1987.

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19

Columbia University. Department of Neurology. Advances in the diagnosis & treatment of neuromuscular disorders and ALS: Featuring the 6th annual Eleanor and Lou Gehrig lecture, Saturday, June 9, 2001 at the Neurological Institute of New York. [New York?]: Columbia University, 2001.

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20

Not in Kansas anymore: A memoir of the farm, New York City, and life with ALS. Winnipeg, Canada: Gemma B. Publishing, 2008.

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21

The butcher's daughter: The story of an army nurse with ALS. College Station, TX: Virtualbookworm.com Pub., 2009.

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22

Gajdusek, D. Carleton. Calcium deficiency induced secondary hyperparathyroidism and resultant CNS deposition of calcium and other metallic cations as the cause of ALS and PD in high incidence among the Auyu and Jakai people in West New Guinea. Bethesda, Md: [National Institute of Neurological and Communicative Disorders and Stroke], 1985.

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23

S, Kazandjian Marta, and Communication Independence for the Neurologically Impaired, Inc., eds. Communication and swallowing solutions for the ALS/MND community: A CINI manual. San Diego: Singular Pub. Group, 1997.

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24

Lou Gehrig Disease, ALS or Amyotrophic Lateral Sclerosis explained: ALS symptoms, signs, stages, types, diagnosis, treatment, caregiver tips, aids and what to expect is all covered. [Ireland]: IMB Publishing, 2013.

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25

Where there is faith He is with you: One woman's journey of faith and her husband's battle with ALS. Decatur, Ill: House of Prayer Ministries, 2011.

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26

Wakefield, Darcy. I remember running: The year I got everything I ever wanted and ALS. New York: Marlowe & Co., 2005.

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27

Robert), Ball Bob (Ball, ed. Elephants in the tea: A journey through ALS. Portland, OR: ACTS Publishers, 2010.

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28

United States. Congress. Senate. A bill to amend the Social Security Act to waive the 24-month waiting period for Medicare coverage of individuals disabled with amyotrophic lateral sclerosis (ALS), and to provide Medicare coverage of drugs and biologicals used for the treatment of ALS or for the alleviation of symptoms relating to ALS. Washington, D.C: U.S. G.P.O., 1999.

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29

Williams, Brian J. (Brian Jeremy), 1976- and American Academy of Orthopaedic Surgeons, eds. Principles of ALS care. Sudbury, Mass: Jones and Bartlett Publishers, 2011.

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30

Sparrow: A journey of grace and miracles while battling ALS. New York: Morehouse Publishing, 2016.

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31

United States. Congress. House. A bill to amend the Social Security Act to waive the 24-month waiting period for Medicare coverage of individuals disabled with amyotrophic lateral sclerosis (ALS), and to provide Medicare coverage of drugs used for treatment of ALS. Washington, D.C: U.S. G.P.O., 1999.

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32

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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33

author, Sands Michael 1962, ed. Hold on, let go: Facing ALS with courage and hope. [North Vancouver, British Columbia]: Influence Publishing, 2015.

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34

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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35

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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36

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

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37

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

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38

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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39

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

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40

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

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41

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

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42

Omlin, Ernest. Amyotrophic Lateral Sclerosis : Genetics Associated W/ ALS: Amyotrophic Lateral Sclerosis Prognosis. Independently Published, 2021.

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43

Nostro, Trista. Amyotrophic Lateral Sclerosis Radiology : History of ALS: Amyotrophic Lateral Sclerosis Symptoms. Independently Published, 2021.

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44

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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45

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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46

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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47

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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48

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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49

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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50

Living with ALS. Calabasas Hills, CA: ALS Association, 2002.

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