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Books on the topic 'Duchenne muscular dystrophy'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 November 2024

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1

Bernardini, Camilla, ed. Duchenne Muscular Dystrophy. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7374-3.

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2

S, Chamberlain Jeffrey, and Rando Thomas A, eds. Duchenne muscular dystrophy: Advances in therapeutics. New York: Taylor & Francis, 2005.

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3

Kate, Stone, ed. Occupational therapy and Duchenne muscular dystrophy. Chichester, West Sussex, England: John Wiley & Sons, 2007.

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4

1932-, Kakulas Byron A., Mastaglia Frank L, and Neuromuscular Foundation of Western Australia., eds. Pathogenesis and therapy of Duchenne and Becker muscular dystrophy. New York: Raven Press, 1990.

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5

1932-, Kakulas Byron A., Howell J. McC, and Roses Allen D, eds. Duchenne muscular dystrophy: Animal models and genetic manipulation. New York: Raven Press, 1992.

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6

Herrmann, Falko H. X-linked muscular dystrophies (Duchenne and Becker): A bibliography. Jena: Universitaẗsbibliothek, 1985.

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7

Herrmann, Falko H. X-linked muscular dystrophies (Duchenne and Becker): A bibliography. Jena: Universitätsbibliothek, 1985.

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8

Herrmann, Falko H. X-linked muscular dystrophies (Duchenne and Becker): A bibliography. Jena: Universita tsbibliothek, 1985.

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9

Bergman, Thomas. Precious time: Children living with muscular dystrophy. Milwaukee: Gareth Stevens Pub., 1996.

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10

Emery, Alan E. H. The history of a genetic disease: Duchenne muscular dystrophy or Meryon's disease. London: Royal Society of Medicne Press, 1995.

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11

H, Emery Marcia L., ed. The history of a genetic disease: Duchenne muscular dystrophy or Meryon's disease. 2nd ed. Oxford [England]: Oxford University Press, 2011.

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12

1958-, Brown Susan C., and Lucy Jack A. 1929-, eds. Dystrophin: Gene, protein, and cell biology. Cambridge, U.K: Cambridge University Press, 1997.

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13

Terence, Partridge, ed. Molecular and cell biology of muscular dystrophy. London: Chapman & Hall, 1993.

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14

Kohen, Yonatan. An Intimacy With Stillness. Tel Aviv: Tzivonim Publishing, 2014.

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15

Hyde, Sylvia A. Duchenne muscular dystrophy: A parent's guide to physiotherapy in the home. London: Muscular Dystrophy Group, 1998.

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16

Smalley, Logan, Julia Eisenman, and Gregory R. Schenz. Darius goes West: The roll of his life. Athens, GA: Darius Goes West, 2008.

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17

Barataud, Bernard. Au nom de nos enfants. Paris: Edition⁰1, 1992.

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18

Harrison, Mary-Ann. The molecular basis of Duchenne muscular dystrophy: Utrophin as a candidate for therapeutic intervention. Sudbury, Ont: Laurentian University, School of Graduate Studies, 2004.

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19

Wilson, Robert Noel. A statistical approach to the detection of Duchenne Muscular Dystrophy carriers using serum enzyme measurements. (s.l: The Author, 1990.

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20

US GOVERNMENT. An Act to Amend the Public Health Service Act to Provide for Research with Respect to Various Forms of Muscular Dystrophy, Including Duchenne, Becker, Limb Girdle, Congenital, Facioscapulohumeral, Myotonic, Oculopharyngeal, Distal, and Emery-Dreifuss Muscular Dystrophies. [Washington, D.C: U.S. G.P.O., 2001.

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21

Duan, Dongsheng. Muscle gene therapy. New York: Springer, 2010.

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22

Lane, H. K. A case study approach to the use of the microcomputer in the education of children with Duchenne muscular dystrophy. Norwich: University of East Anglia, 1986.

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23

I, Charash Leon, ed. Realities in coping with progressive neuromuscular diseases. Philadelphia, Pa: Charles Press Publishers, 1987.

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24

Chamberlain, Jeffrey S., and Thomas A. Rando, eds. Duchenne Muscular Dystrophy. CRC Press, 2006. http://dx.doi.org/10.3109/9780849374456.

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25

Duchenne muscular dystrophy. 2nd ed. Oxford: Oxford University Press, 1993.

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26

Duchenne muscular dystrophy. Oxford University Press, 1988.

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27

Duchenne muscular dystrophy. Oxford: Oxford University Press, 1987.

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28

Duchenne Muscular Dystrophy. CRC, 1996.

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29

Duchenne Muscular Dystrophy. Oxford University Press, Incorporated, 2015.

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30

Duchenne muscular dystrophy. 3rd ed. Oxford: Oxford University Press, 2003.

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31

Duchenne Muscular Dystrophy. Oxford University Press, 2015.

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32

Kreeger, Renee Nierman, and James P. Spaeth. Muscular Dystrophy. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199764495.003.0063.

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Gastrostomy tube placement is typically a routine surgical procedure with little concern for morbidity and mortality. However, in patients with Duchenne muscular dystrophy (DMD), this is not the case. Patients with DMD present a unique clinical dilemma since they often do not require gastrostomy tube placement until their physical status has deteriorated to the point that they have respiratory insufficiency or failure and clinically significant cardiomyopathy. An understanding of the pathophysiology of this disorder and a proactive approach to perioperative management are important to ensure a positive patient outcome.

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33

Duchenne Muscular Dystrophy: Advances in Therapeutics (Neurological Disease and Therapy). Informa Healthcare, 2006.

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34

Kreeger, Renee, and James P. Spaeth. Muscular Dystrophy. Edited by Erin S. Williams, Olutoyin A. Olutoye, Catherine P. Seipel, and Titilopemi A. O. Aina. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190678333.003.0058.

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Duchenne muscular dystrophy (DMD) is a complex disease characterized by multiple physiologic perturbations, progressively leading to cardiomyopathy, respiratory failure, and, eventually, death. Patients with DMD create unique challenges for the anesthesia team, including management of a difficult airway, avoidance of volatile anesthetics and succinylcholine, the need for respiratory support, and discussion of advance directives. A thorough and multidisciplinary collaborative approach must be utilized in the care of these patients for the entire perioperative period. This chapter uses a case example of a 17-year-old boy with DMD who presents for preoperative anesthesia consultation in anticipation of percutaneous endoscopic gastrostomy tube placement.

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35

Bernardini, Camilla. Duchenne Muscular Dystrophy: Methods and Protocols. Springer New York, 2017.

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36

Bernardini, Camilla. Duchenne Muscular Dystrophy: Methods and Protocols. Springer New York, 2018.

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37

Blakeney, Joy, Alex Howarth, Hether McAndrew, Mary McCutcheon, and Kate Stone. Occupational Therapy and Duchenne Muscular Dystrophy. Wiley & Sons, Limited, John, 2008.

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38

Chamberlain, Jeffrey S., and Thomas A. Rando. Duchenne Muscular Dystrophy: Advances in Therapeutics. Taylor & Francis Group, 2006.

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39

Fitzpatrick, Carol. Psychiatric disorder in Duchenne muscular dystrophy. 1991.

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40

Chamberlain, Jeffrey S., and Thomas A. Rando. Duchenne Muscular Dystrophy: Advances in Therapeutics. Taylor & Francis Group, 2006.

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41

Tester, Claire, Joy Blakeney, Alex Howarth, Hether McAndrew, and Kate Stone. Occupational Therapy and Duchenne Muscular Dystrophy. Wiley & Sons, Incorporated, John, 2007.

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42

Tester, Claire, Joy Blakeney, Alex Howarth, Hether McAndrew, and Kate Stone. Occupational Therapy and Duchenne Muscular Dystrophy. Wiley & Sons, Incorporated, John, 2007.

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43

Occupational Therapy and Duchenne Muscular Dystrophy. Wiley, 2007.

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44

Honorio, Samuel Alexandre Almeida. Duchenne Muscular Dystrophy: Symptoms, Management and Prognosis. Nova Science Publishers, Incorporated, 2015.

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45

Emery, Alan E. H., and Marcia L. H. Emery. Early history of muscular dystrophy. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199591473.003.0002.

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46

Moonrise: One Family, Genetic Identity, and Muscular Dystrophy. St. Martin's Griffin, 2004.

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47

Moonrise: One Family, Genetic Identity, and Muscular Dystrophy. St. Martin's Press, 2003.

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48

McChowell, John. Duchenne Muscular Dystrophy: Animal Models and Genetic Manipulation. Raven Press Ltd, 1992.

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49

Guide to Duchenne Muscular Dystrophy: Information and Advice for Teachers and Parents. Kingsley Publishers, Jessica, 2017.

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50

Muntoni, Francesco, Janet Hoskin, Kate Maresh, Veronica Hinton, and Lianne Abbot. Guide to Duchenne Muscular Dystrophy: Information and Advice for Teachers and Parents. Kingsley Publishers, Jessica, 2017.

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