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Relevant bibliographies by topics / Muscular dystrophy / Books

Books on the topic 'Muscular dystrophy'

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Author: Grafiati

Published: 4 June 2021

Last updated: 10 March 2023

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1

Muscular dystrophy. New York: F. Watts, 1992.

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2

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

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3

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

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4

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

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5

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

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6

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

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7

Muscular dystrophy. Oxford: Oxford University Press, 1994.

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8

Burnett, Gail Lemley. Muscular dystrophy. Parsippany, N.J: Crestwood House, 1996.

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9

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

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10

Muscular dystrophy. Detroit: Lucent Books, 2008.

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11

D, Rioux Stephen, and Wong Brenda M. D, eds. Muscular dystrophy. Berkeley Heights, NJ: Enslow Publishers, 2000.

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12

Johanson, Paula. Muscular dystrophy. New York: Rosen Pub. Group, 2008.

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13

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

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14

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

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15

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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16

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

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17

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

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18

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

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19

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

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20

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

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21

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

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22

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

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23

Muscular dystrophies. Amsterdam: Elsevier, 2011.

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24

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

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25

H, Emery Alan E., ed. The muscular dystrophies. Oxford, England: Oxford University Press, 2001.

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26

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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27

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

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28

Muscular Dystrophy: Lived Experience of Mother. Saarbrücken: LAP LAMBERT Academic Publishing, 2014.

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29

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

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30

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

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31

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

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32

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

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33

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

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34

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. Amsterdam: Excerpta Medica, 1991.

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35

Myoblast transfer: Gene therapy for muscular dystrophy. Austin: R.G. Landes, 1994.

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36

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

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37

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

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38

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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39

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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40

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

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41

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

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42

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

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43

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

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44

Muscular Dystrophy. Oxford University Press, Incorporated, 2008.

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45

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

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46

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

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47

Duchenne Muscular Dystrophy. Oxford University Press, 2015.

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48

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 and postoperative ventilation. The chapter covers an overview of the disease; etiology and pathogenesis; cognitive, neuromuscular, cardiac, and pulmonary clinical presentation; diagnosis and management; and special anesthetic considerations.

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49

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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50

Duchenne Muscular Dystrophy. CRC, 1996.

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