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Books on the topic 'Muscular dystrophy'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Naff, Clay Farris. Muscular dystrophy. Greenhaven Press, 2011.

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2

Bushby, Katherine M. D., and Louise V. B. Anderson. Muscular Dystrophy. Humana Press, 2001. http://dx.doi.org/10.1385/1592591388.

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3

Emery, Alan E. H. Muscular dystrophy. 3rd ed. Oxford University Press Inc., 2008.

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4

Huml, Raymond A., ed. Muscular Dystrophy. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-17362-7.

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5

D, Rioux Stephen, and Wong Brenda M. D, eds. Muscular dystrophy. Enslow Publishers, 2000.

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6

Johanson, Paula. Muscular dystrophy. Rosen Pub. Group, 2008.

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7

Emery, Alan E. H. Muscular dystrophy. 3rd ed. Oxford University Press Inc., 2008.

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8

Burnett, Gail Lemley. Muscular dystrophy. Crestwood House, 1996.

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9

Nene College. Nene Centre for Health Care Education. Occupational Therapy Course Team. Muscular Dystrophy. Nene College, 1987.

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10

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

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11

Maruyama, Rika, and Toshifumi Yokota, eds. Muscular Dystrophy Therapeutics. Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-2772-3.

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12

Emery, Alan E. H. Muscular dystrophy, the facts. 2nd ed. Oxford University Press, 2000.

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13

H, Ruben Douglas, and Macciomei Nancy R, eds. Readings in muscular dystrophy. Longman, 1986.

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14

Takeda, Shin'ichi, Yuko Miyagoe-Suzuki, and Madoka Mori-Yoshimura, eds. Translational Research in Muscular Dystrophy. Springer Japan, 2016. http://dx.doi.org/10.1007/978-4-431-55678-7.

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15

D, Bushby Katharine M., and Anderson Louise V. B, eds. Muscular dystrophy: Methods and protocols. Humana, 2001.

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16

N, Burgess V., ed. Trends in muscular dystrophy research. Nova Science Publishers, 2005.

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17

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

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18

J, Winder Steve, ed. Molecular mechanisms of muscular dystrophies. Landes Bioscience : Eurekah.com, 2006.

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19

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

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20

Kate, Stone, ed. Occupational therapy and Duchenne muscular dystrophy. John Wiley & Sons, 2007.

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21

C, Angelini, Danieli Gian Antonio 1942-, Fontanari D, and International Congress on Neuromuscular Diseases (7th : 1990 : Munich, Germany), eds. Muscular dystrophy research: From molecular diagnosis toward therapy : proceedings of the Satellite Symposium on Muscular Dystrophy Research 90, Venice, Italy, 14-15 September 1990, held in conjunction with the VIIth International Congress on Neuromuscular Diseases, Munich, Germany, 16-22 September 1990. Excerpta Medica, 1991.

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22

Sugita, Hideo. Kin-jisutorofī-shō oyobi kanren shikkan no byōtai to sono byōin ni kansuru kenkyū: Shōwa 63-nendo kenkyū hōkokusho. s.n.], 1989.

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23

Iida, Mitsuo. Kin-jisutorofī no ryōyō to kango ni kansuru sōgōteki kenkyū: Kenkyū seika hōkokusho. s.n.], 1991.

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24

Sugita, Hideo. Kin-jisutorofī-shō oyobi kanren shikkan no byōtai to sono byōin ni kansuru kenkyū: Heisei gannendo kenkyū hōkokusho. s.n.], 1990.

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25

Sugita, Hideo. Kin-jisutorofī-shō oyobi kanren shikkan no byōtai to sono byōin ni kansuru kenkyū: Shōwa 62-nendo kenkyū hōkokusho. Sugita-han?, 1988.

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26

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

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27

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

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28

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

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29

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

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30

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 ex

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31

Hegde, Madhuri, ed. Muscular Dystrophy. InTech, 2012. http://dx.doi.org/10.5772/1242.

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32

Muscular dystrophy. F. Watts, 1992.

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33

Muscular Dystrophy. Rosen Publishing Group, 2008.

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34

Muscular dystrophy. Oxford University Press, 1994.

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35

Muscular dystrophy. Lucent Books, 2008.

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36

Johanson, Paula. Muscular Dystrophy. Rosen Publishing Group, 2008.

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37

Naff, Clay Farris. Muscular Dystrophy. Greenhaven Publishing LLC, 2011.

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38

Emery, Alan E. H. Muscular Dystrophy. Oxford University Press, 2014.

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39

Mousa, Nahla O., Francisco Hernandez-Torres, and Robin Warner. Muscular Dystrophy. DI Press, 2022.

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40

Muscular Dystrophy. Oxford University Press, Incorporated, 2008.

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41

Muscular Dystrophy. Rosen Publishing Group, 2009.

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42

Muscular Dystrophy: A Guide to Understanding Muscular Dystrophy. Independently Published, 2021.

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43

Sutherland, Tori N., and Kirk Lalwani. Duchenne’s Muscular Dystrophy. Edited by Kirk Lalwani, Ira Todd Cohen, Ellen Y. Choi, and Vidya T. Raman. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190685157.003.0035.

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Duchenne’s muscular dystrophy (DMD) is a progressive X-linked recessive disorder that affects boys and female carriers. It is the most common dystrophy with onset in childhood in the United States. It is associated with severe, progressive proximal muscle weakening due to absence of dystrophin, which is found in skeletal and cardiac muscles This chapter presents a review of anesthetic considerations for patients with DMD in the context of the disease’s natural history with special consideration for cardiomyopathy evaluation and management, restrictive lung disease evaluation, and management an

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44

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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45

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

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46

Duchenne muscular dystrophy. Oxford University Press, 1988.

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47

Duchenne muscular dystrophy. Oxford University Press, 1987.

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48

Emery, Alan E. H. Muscular Dystrophy (Directions). 3rd ed. Oxford University Press, USA, 2008.

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49

Duchenne Muscular Dystrophy. CRC, 1996.

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50

Understanding Muscular Dystrophy. FOSTER ACADEMICS, 2015.

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