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Books on the topic 'Chorée de Huntington'

Author: Grafiati

Published: 4 June 2021

Last updated: 31 August 2024

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1

Sanberg, Paul R. Cell transplantation for Huntington's disease. R.G. Landes, 1994.

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2

Sanberg, Paul R. Cell transplantation for Huntington's disease. R.G. Landes, 1994.

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3

Wexler, Alice. The woman who walked into the sea: Huntington's and the making of a genetic disease. Yale University Press, 2008.

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4

Gillian, Bates, Harper Peter S, and Jones Lesley 1957-, eds. Huntington's disease. 3rd ed. Oxford University Press, 2002.

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5

C, Lo Donald, and Hughes, Robert E., Ph.D., eds. Neurobiology of Huntington's disease: Applications to drug discovery. CRC Press/Taylor & Francis Group, 2010.

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6

Oliver, Quarrell, ed. Juvenile Huntington's disease: (and other trinucleotide repeat disorders). Oxford University Press, 2009.

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7

Pollard, Jim. A caregiver's handbook for advanced-stage Huntington's disease / author and editor, Jim Pollard ; contributors, Rosemary Best ... [et. al]. Huntington's Disease Society of America, 1999.

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8

Timothy, Bishop D., Falk Catherine T, MacCluer Jean W, and Genetic Analysis Workshop (4th : 1985 : Snowbird, Utah), eds. Genetic epidemiology: Applications and comparisons of methods. Liss, 1987.

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9

Adam, Rosenblatt, Huntington's Disease Society of America (New York, N.Y.)., and Foundation for the Care and Cure of Huntington's Disease., eds. A physician's guide to the management of Huntington's disease. 2nd ed. Huntington's Disease Society of America, 1999.

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10

Wexler, Alice. Mapping fate: A memoir of family, risk, and genetic research. University of California Press, 1995.

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11

Dalby, S. N. Facing Huntington's chorea: A handbook for families and friends. 2nd ed. Association to Combat Huntingdon's Chorea, 1988.

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12

Paulsen, Jane S. Understanding behavior in Huntington's disease: A practical guide for individuals, families, and professionals coping with HD. 2nd ed. Huntington's Disease Society of America, 1999.

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13

Werbel, Eileen. Toward a fuller life: A guide to everyday living with Huntington's disease. Huntington's Disease Society of America, 1990.

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14

Clipper, Stephanie E. Huntington's disease: Hope through research. The Institutes, 1998.

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15

Quarrell, Oliver. Huntington's disease: The facts. 2nd ed. Oxford University Press, 2008.

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16

Association, Scottish Huntingdon's. Opening doors: A compilation of short stories, personal accounts, paintings and drawings from people whose lives have been touched by Huntingdon's Disease. Scottish Huntingdon's Association, 1998.

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17

Association, Scottish Huntingdon's. Facing Huntington's disease: A handbook for families and friends. Scottish Huntingdon's Association, 1998.

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18

Naff, Clay Farris. Huntington's disease. Greenhaven Press, 2012.

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19

Yount, Lynette Ann. Caffeine killed my family: Best free cure since Jesus Christ himself. Xlibris Corp., 2007.

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20

1951-, Pincus Harold Alan, Pardes Herbert 1934-, and American Psychiatric Association Meeting, eds. The Integration of neuroscience and psychiatry. American Psychiatric Press, 1985.

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21

Job Accommodation Network (U.S.). Job accommodations for people with Huntington's disease. Office of Disability Employment Policy, Job Accommodation Network, 2010.

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22

Parker, Philip M., and James N. Parker. Huntington disease: A medical dictionary, bibliography, and annotated research guide to Internet references. ICON Health Publications, 2004.

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23

Green, Holly. Don't slam the door! Publishingworks, 2004.

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24

Parker, James N., and Philip M. Parker. Huntington disease: A bibliography and dictionary for physicians, patients, and genome researchers [to internet references]. ICON Health Publications, 2007.

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25

Parker, Philip M., and James N. Parker. Huntington's disease: A medical dictionary, bibliography, and annotated research guide to Internet references. ICON Health Publications, 2003.

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26

Fay, Juliette. The shortest way home. Penguin Books, 2013.

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27

Tullson, Diane. Saving Jasey. Orca Book Publishers, 2002.

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28

Kraus, Harry Lee. For the rest of my life. Zondervan, 2003.

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29

Kraus, Harry Lee. Could I have this dance?: Harry Kraus. Zondervan, 2002.

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30

United States. Congress. House. A bill to require the Commissioner of Social Security to revise the medical criteria for evaluating disability in a person diagnosed with Huntington's disease and to waive the 24-month waiting period for Medicare eligibility for individuals disabled by Huntington's disease. U.S. G.P.O., 2008.

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31

Sadleir, Michael. Fanny by Gaslight. Arrow (A Division of Random House Group), 1986.

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32

Rivières, Alice. Testing Knowledge: Toward an Ecology of Diagnosis, Preceded by the Dingdingdong Manifesto. Punctum Books, 2021.

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33

Tabrizi, Sarah, Gillian Bates, and Lesley Jones. Huntington's Disease. Oxford University Press, Incorporated, 2014.

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34

Huntington's Disease. 2nd ed. W.B. Saunders Company, 1996.

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35

Anderson, Karen E., and Andrew S. Feigin. Huntington Disease. Elsevier Science & Technology Books, 2017.

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36

Precious, Sophie V., Anne E. Rosser, and Stephen B. Dunnett. Huntington's Disease. Springer New York, 2018.

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37

Bates, Gillian P., and Sarah J. Tabrizi. Huntington's Disease. Oxford University Press, Incorporated, 2014.

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38

Precious, Sophie V., Anne E. Rosser, and Stephen B. Dunnett. Huntington's Disease. Springer New York, 2019.

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39

Quarrell, Oliver W. Huntington's Disease. Oxford University Press, 2014.

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40

Venuto, Charles S., and Karl Kieburtz. Huntington Disease. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0008.

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The clinical management of Huntington’s disease entails pharmacologic interventions and nonpharmacologic supportive therapy. There are no treatments that can halt or alter the progression of disease, therefore the goal is to maximize function and optimize quality of life. Tetrabenazine is the only pharmacologic agent with regulatory approval for Huntington’s disease chorea; however, off-label use of antidopaminergic agents is common. Treatment of behavioral disturbances can be tailored to the specific symptoms by using antidepressant, antipsychotic, and anxiolytic agents. Clinical trials testi

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41

Hughes, Robert E., and Donald C. Lo. Neurobiology of Huntington's Disease: Applications to Drug Discovery. Taylor & Francis Group, 2010.

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42

Hughes, Robert E., and Donald C. Lo. Neurobiology of Huntington's Disease: Applications to Drug Discovery. Taylor & Francis Group, 2010.

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43

Hughes, Robert E., and Donald C. Lo. Neurobiology of Huntington's Disease: Applications to Drug Discovery. Taylor & Francis Group, 2017.

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44

Quarrell, Oliver. Huntington's Disease. 3rd ed. Oxford University Press, 2020. http://dx.doi.org/10.1093/oso/9780198844389.001.0001.

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Abstract:

Huntington’s disease (HD)―the facts provides an overview of the condition aimed at families and carers understanding the condition. It describes the key features of: a movement disorder, disturbance of mood (affect), and problems with thinking (cognition) and behaviour. The movement problems of chorea, dystonia, and bradykinesia are explained but there is equal emphasis on depression impulsive behaviour and temper outbursts. Understanding the cause of these may help families cope better when they arise. The genetic change is discussed as is its effect on the protein huntingtin. Options for gen

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45

Bird, Thomas D. Can You Help Me?: Inside the Turbulent World of Huntington Disease. Oxford University Press, Incorporated, 2019.

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46

Hughes, Christina. Huntington's Disease: Prevalence, Pathogenesis and Treatment. Nova Science Publishers, Incorporated, 2017.

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47

Anderson, Karen E., and Andrew S. Feigin. SPEC - Handbook of Clinical Neurology, Volume 144, Huntington Disease, 12-Month Access, EBook. Elsevier Science & Technology Books, 2017.

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48

Watt, David C. Clinico-Genetic Study of Psychiatric Disorder in Huntington's Chorea. University of Cambridge ESOL Examinations, 2016.

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49

Anderson, Karen E., and Andrew S. Feigin. SPEC - Handbook of Clinical Neurology, Volume 144, Huntington Disease, 12-Month Access, EBook. Elsevier, 2019.

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50

A Clinico-Genetic Study of Psychiatric Disorder in Huntington's Chorea (Psychological Medicine Supplements). Cambridge University Press, 1994.

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