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Libros sobre el tema "Duchenne Muscular Dystrophy (DMD)"

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Publicado: 4 de junio de 2021
Última modificación: 25 de julio de 2025

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1

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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2

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

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3

Kate, Stone, ed. Occupational therapy and Duchenne muscular dystrophy. 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. Raven Press, 1990.

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5

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

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6

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

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7

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

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8

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

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9

Bergman, Thomas. Precious time: Children living with muscular dystrophy. 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. 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 University Press, 2011.

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12

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

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13

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

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14

Kohen, Yonatan. An Intimacy With Stillness. Tzivonim Publishing, 2014.

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15

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

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16

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

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17

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

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18

Harrison, Mary-Ann. The molecular basis of Duchenne muscular dystrophy: Utrophin as a candidate for therapeutic intervention. 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. 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. U.S. G.P.O., 2001.

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21

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

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22

Duan, Dongsheng. Muscle gene therapy. Springer, 2010.

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23

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

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24

Duchenne Muscular Dystrophy. Exon Publications, 2024. http://dx.doi.org/10.36255/duchenne-muscular-dystrophy.

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Duchenne Muscular Dystrophy (DMD) is a severe genetic disorder that affects the muscles, causing them to weaken over time. This condition primarily impacts boys and leads to progressive physical disability, requiring comprehensive care and management. This guide provides an accessible yet detailed explanation of DMD, addressing its causes, inheritance patterns, symptoms, diagnosis, treatment, and daily management. The content is designed to serve as a valuable resource for patients, families, and caregivers seeking clarity on this condition. Understanding the role of the dystrophin gene and ex
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25

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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26

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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27

Dan & DMD: A Children's Book on Duchenne Muscular Dystrophy. CreateSpace Independent Publishing Platform, 2016.

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28

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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29

Griffiths, Ian A. Dmd Life Art and Me. Grosvenor House Publishing Limited, 2010.

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30

Nageshwaran, Sathiji, Heather C. Wilson, Anthony Dickenson, and David Ledingham. Disorders of muscle and neuromuscular junction. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199664368.003.0008.

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This chapter discusses the clinical features and evidence base for the pharmacological treatment of muscular disorders (inflammatory myopathies: polymyositis, dermatomyositis, and inclusion body myositis), mitochondrial myopathies, Duchenne muscular dystrophy (DMD), myotonic dystrophy, inherited neuromuscular channelopathies, non-dystrophic myotonias (myotonia congenita, paramyotonia congenita), periodic paralyses, acquired neuromyotonia (Isaac syndrome and Morvan syndrome), stiff person syndrome, and disorders of the neuromuscular junction (myasthenia gravis (MG), myasthenic crisis, and Lambe
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31

Firth, Helen V., Jane A. Hurst, and Judith G. Hall. Appendix. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780192628961.003.0204.

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Bayes’ theorem 646Behavioural pattern profile (Shalev and Hall 2004) 648Carrier frequency and carrier testing for autosomal recessive disorders 650Centile charts for boys height and weight 652Centile charts for girls height and weight 656Centile charts for occipital-frontal circumference (OFC) 660CK (Creatine kinase) levels in carriers of Duchenne muscular dystrophy (DMD) ...
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32

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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33

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

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34

Duchenne muscular dystrophy. Oxford University Press, 1988.

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35

Duchenne muscular dystrophy. Oxford University Press, 1987.

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36

Duchenne Muscular Dystrophy. CRC, 1996.

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37

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

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38

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

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39

Duchenne Muscular Dystrophy. Oxford University Press, 2015.

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40

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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41

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

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42

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

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43

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

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44

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

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45

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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46

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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47

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

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48

Occupational Therapy and Duchenne Muscular Dystrophy. Wiley, 2007.

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49

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

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50

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

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