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Books on the topic 'MND'

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Author: Grafiati

Published: 4 June 2021

Last updated: 10 March 2023

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1

Hurlic, Susan. MND, mulheres no desenvolvimento. [Luanda]: Ler & Escrever, 1992.

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2

Blank, Robert H., Jerome E. Kurent, and David Oliver, eds. Public Policy in ALS/MND Care. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-5840-5.

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3

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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4

Association, Motor Neurone Disease, ed. MND resource file: A patient and carer centred approach for health & social care professionals. Northampton: Motor Neurone Disease Association, 2000.

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5

Payback: The case for revenge. Chicago: The University of Chicago Press, 2013.

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6

Ayob, Osman. Mad Mid Mod. 2nd ed. Kuala Lumpur: Fajar Pakeer, 2010.

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7

The insane train. New York: Minotaur Books, 2010.

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8

Tikkanen, Märta. Sofia vuxen med sitt MBD. 2nd ed. [Stockholm]: Forum, 1998.

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9

Cruces, Steven. A mind made mad: A poetic disturbance. Miami, Fla: S. Cruces, 1997.

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10

Appignanesi, Lisa. Mad, bad, and sad: Women and the mind doctors. New York: W. W. Norton & Co., 2008.

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11

Mid-century ads: Advertising from the Mad Men era. Köln: Taschen, 2012.

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12

Helle, Helle. Forestillingen om et ukompliceret liv med en mand: Roman. København: Samleren, 2002.

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13

Kapoor, Raj. Mend the mind, mind the body, meet the soul: Exploring the secrets of health & longevity. Fort Bragg, Calif: Lost Coast, 1998.

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14

Yardley, Jonathan. States of mind: A personal journey through the Mid-Atlantic. New York: Villard Books, 1993.

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15

Queen Victoria's skull: [George Combe and the mid-Victorian mind]. London: Hambledon Continuum, 2008.

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16

Sad, mad and bad: Women and the mind-doctors from 1800. Toronto: McArthur & Co., 2007.

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17

Mid-Victorian imperialists: British gentleman and the empire of the mind. London: Routledge, 2005.

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18

Appignanesi, Lisa. Sad, mad and bad: Women and the mind-doctors from 1800. Toronto: McArthur & Co., 2007.

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19

Sad, mad and bad: Women and the mind-doctors from 1800. Toronto, ON: McArthur & Co., 2007.

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20

Lisa, Tener, and Todd Peaco, eds. Good and mad: Transform anger using mind, body, soul, and humor. Deerfield Beach, Fla: Health Communications Inc., 2003.

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21

The mad, the bad and the innocent: The criminal mind on trial. New York: Harper Collins, 1997.

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22

The mad, the bad, and the innocent: The criminal mind on trial. Boston: Little, Brown, 1997.

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23

Rose, F. Clifford. New Evidence in MND/ALS Research (Advances in ALS/MND). Smith-Gordon & Co Ltd, 1991.

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24

Terrell, Tracy. Gen Cmb Deux Mnd; Wblm. McGraw-Hill Education, 2015.

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25

Terrell, Tracy. Gen Cmb Deux Mnd; Wblm. McGraw-Hill Education, 2015.

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26

Terrell, Tracy. Gen Cmb Deux Mnd; Cnct+. McGraw-Hill Education, 2015.

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27

Terrell, Tracy. GEN CMB DEUX MND; CNCT. McGraw-Hill Education, 2015.

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28

Terrell, Tracy D. Gen Cmb Ll Deux Mnd; Cnct+. McGraw-Hill Education, 2015.

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29

NA. Psyco Brain Persn& Mnd Mattr CD& Lab Strt Kit. Addison Wesley Publishing Company, 2003.

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30

Blank, Robert H., Jerome E. Kurent, and David Oliver. Public Policy in ALS/MND Care: An International Perspective. Springer Singapore Pte. Limited, 2021.

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31

NA. Psych Perspct&contemp Rd&mnd Mttrs CD&Sg Pk. Addison Wesley Longman, 2001.

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32

Public Policy in ALS/MND Care: An International Perspective. Palgrave Macmillan, 2020.

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33

NA. Psycholgy Sci of Behv& A& B Mnd Mattr& Strt Sg. Addison Wesley Publishing Company, 2003.

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34

NA. Undstndg Humn Behv& Stdy GD& A& B Mnd Mttr& BB. Addison Wesley Publishing Company, 2004.

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35

Noble, Lynne D. M. MND Diet: Using Nutrition to Slow down the Progression of Neurodegeneration. Independently Published, 2018.

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36

NA. Ess Psych with I/A Pin& A& B Mnd Mttrs CD& GD. Addison Wesley Publishing Company, 2003.

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37

Kavanagh, Noel. From Living the Dream to Living with MND: A Race Against Time. On Stream Publications, Limited, 2021.

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38

Communication And Swallowing Solutions for the ALS/MND Community: A CINI Manual. Singular, 1996.

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39

Alexander, Joshua, David J. Croteau, and Ronald J. Ellis. HIV-Associated Neurocognitive Disorders. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0147.

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Three subclassifications of HIV Associated Neurocognitive Disorders (HAND) can be delineated: asymptomatic neurocognitive impairment (ANI), mild neurocognitive disorder (MND), and HIV-associated dementia (HAD). HAND occurs in about half of patients infected with HIV. All forms, including ANI and MND, are associated with unemployment and reduced antiretroviral adherence, which can lead to loss of virologic suppression, further neurocognitive decline, and systemic illness. Fortunately, combined antiretroviral therapy can stabilize and even reverse cognitive impairment.

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40

Weir, Stewart, and Doddie Weir. Doddie's Diary: The Highs, the Lows and the Laughter from My Fight with MND. Black and White Publishing Limited, 2022.

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41

Note, Simple. Note: Simple Notebook Multicolor 120 Pages Lined for Men Mnd Women Writing Notebook Diary. Independently Published, 2020.

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42

Rose, F. Clifford. ALS - From Charcot to the Present and into the Future (Advances in ALS/MND). Smith-Gordon & Co Ltd, 1994.

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43

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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44

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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45

Nageshwaran, Sathiji, Heather C. Wilson, Anthony Dickenson, and David Ledingham. Disorders of peripheral nerves and motor neuron disease. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199664368.003.0007.

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This chapter discusses the clinical features and evidence-based drug treatment regimens of polyneuropathies (Guillain–Barré syndrome (GBS), chronic inflammatory demyelinating polyneuropathy (CIDP), multifocal motor neuropathy, paraproteinaemic neuropathies, and vasculitic neuropathies), mononeuropathies (Bell’s palsy), systemic conditions with peripheral nerve involvement (Sjögren’s and sarcoidosis), and motor neuron disease (MND).

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46

Shaw, Pamela. The motor neurone disorders. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198569381.003.0524.

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The motor neurone diseases are a group of disorders in which there is selective loss of function of upper and/or lower motor neurones in the motor cortex, brainstem, and spinal cord resulting in impairment in the nervous system control of voluntary movement. The term ‘motor neurone disease’, often abbreviated to ‘MND’, is used differently in different countries. In the United Kingdom it is used as an umbrella term to cover the related group of neurodegenerative disorders including amyotrophic lateral sclerosis, the commonest variant, as well as progressive muscular atrophy, primary lateral sclerosis, and progressive bulbar palsy. However, in many other countries amyotrophic lateral sclerosis, referred to as ALS, has been adopted as the umbrella term for this group of clinical variants of motor system degeneration. There is a tendency now internationally to use the ALS/MND abbreviation to cover this group of conditions. Careful diagnosis within the motor neurone diseases is essential for advising about prognosis, potential genetic implications, and for identifying those with acquired lower motor neurone syndromes who may benefit for the administration of immunomodulatory therapy.

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47

Rosenbaum, Thane. Payback: The Case for Revenge. University of Chicago Press, 2013.

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48

Shaibani, Aziz. Muscle Stiffness and Cramps. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190661304.003.0020.

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Muscle stiffness as a nonspecific term means limited muscle mobility. Muscle and joint pain may be described as stiffness. Painful, sustained muscle cramps are usually associated with muscle stiffness. A careful history is paramount. Exercise-induced muscle cramps are usually myopathic (metabolic or mitochondrial myopathy) while resting, and nocturnal cramps are neurogenic [neuropathy, motor neuron disease (MND), etc.]. Metabolic cramps are electrically silent. Focal or generalized stiffness is typically seen in stiff person syndrome (SPS). Upper motor neuron (UMN) lesions are associated with spasticity and stiffness [hereditary spastic paraplegia (HSP), primary lateral sclerosis (PLS), myelopathies, etc.]. Painful cramps and fasciculation are important clues to peripheral nerve hyperexcitability disorder, which may also present with neuromyotonia. Not unusually, no cause is found for muscle cramps and stiffness. Symptomatic treatment frequently helps.

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49

Drucker, Mort. M.D. Mad Show Stop. Warner Books, 1985.

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50

Shahi, Saurabhi. Tame the Mad Mind. Notion Press, 2021.

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