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Books on the topic 'Dystrophy'

Author: Grafiati
Published: 4 June 2021
Last updated: 30 July 2024

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1

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

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2

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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3

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

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4

Harper, Peter S. Myotonic dystrophy. 2nd ed. New York: Oxford University Press, 2009.

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5

Takahashi, Masanori P., and Tsuyoshi Matsumura, eds. Myotonic Dystrophy. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-13-0508-5.

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6

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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7

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

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8

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

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9

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

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10

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

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11

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

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12

Shinichi, Ohno, and Kobayashi T. (Takayoshi), eds. Myotonic dystrophy and myotonic dystrophy protein kinase. Jena, Germany: Urban & Fischer, 2000.

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13

Ueda, Hideho. Myotonic dystrophy and myotonic dystrophy protein kinase. Jena, Germany: Urban & Fischer, 2000.

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14

Stanton-Hicks, Michael, Wilfrid Jänig, and Robert A. Boas, eds. Reflex Sympathetic Dystrophy. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-0685-6.

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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

d'A, Stanton-Hicks Michael, Jänig Wilfrid, and Boas Robert A, eds. Reflex sympathetic dystrophy. Boston: Kluwer Academic Publishers, 1990.

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18

Zahid, Sarwar, Kari Branham, Dana Schlegel, Mark E. Pennesi, Michel Michaelides, John Heckenlively, and Thiran Jayasundera. Retinal Dystrophy Gene Atlas. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-10867-4.

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19

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

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20

Williams, Roger. RSD: Reflex sympathetic dystrophy. Bethesda, MD: American Occupational Therapy Association, 1995.

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21

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

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22

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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23

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

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24

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

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25

Wilfrid, Jänig, and Stanton-Hicks Michael d'A, eds. Reflex sympathetic dystrophy: A reappraisal. Seattle: IASP Press, 1995.

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26

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

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27

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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28

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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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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Abstract:
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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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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Abstract:
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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31

Johnson, Andrea. Myotonic 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/9780190685157.003.0034.

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Abstract:
Myotonic dystrophy (DM) is a multisystemic autosomal dominant disorder. Individuals may present with symptoms at any age, but pediatric patients typically will present before 10 years of age. The clinical features of DM differ depending on the type of dystrophy and include skeletal muscle weakness, myotonia, sleep apnea, decreased gastrointestinal motility, insulin hypersecretion, cardiac conduction abnormalities, and occasionally cognitive impairment. Anesthetic management of the patient with DM should begin in the preoperative arena and should take into account the postoperative considerations and concerns for the patient with DM. This chapter will help the clinician develop an appropriate anesthetic plan and implement a safe and effective perioperative experience.
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32

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

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33

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

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34

Muscular Dystrophy. Rosen Publishing Group, 2008.

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35

Muscular dystrophy. Oxford: Oxford University Press, 1994.

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36

Muscular dystrophy. Detroit: Lucent Books, 2008.

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37

Myotonic Dystrophy. 3rd ed. Bailliere Tindall, 2001.

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38

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

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39

of, American Academy. Fuchs' Dystrophy. American Academy of Ophthalmology, 2014.

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40

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

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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

Muscular Dystrophy. Oxford University Press, Incorporated, 2008.

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44

Muscular Dystrophy. Rosen Publishing Group, 2009.

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45

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

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46

Jänig, Wilfrid, Michael Stanton-Hicks, and Robert A. Boas. Reflex Sympathetic Dystrophy. Springer, 2011.

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47

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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Abstract:
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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48

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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49

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

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50

Duchenne muscular dystrophy. Oxford University Press, 1988.

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