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Libri sul tema "Duchenne Muscular Dystrophy (DMD)"

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Autore: Grafiati

Pubblicato: 4 giugno 2021

Ultima modifica: 21 febbraio 2023

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1

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

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2

Emery, Alan E. H. Duchenne muscular dystrophy. 3^a ed. Oxford: Oxford University Press, 2003.

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3

Bernardini, Camilla, a cura di. 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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4

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

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5

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

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6

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

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7

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

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8

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

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9

Wan, Philip. Voices of hope: Coping with muscular dystrophy in Mauritius. Port-Louis: Best Graphics Ltd., 2008.

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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., a cura di. The history of a genetic disease: Duchenne muscular dystrophy or Meryon's disease. 2^a ed. Oxford [England]: Oxford University Press, 2011.

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12

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

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13

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

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14

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

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15

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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16

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

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17

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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18

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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19

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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20

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

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21

Muscle gene therapy: Methods and protocols. New York, NY: Humana, 2011.

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22

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

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Abstract (sommario):

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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23

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

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Abstract (sommario):

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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24

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

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25

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

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Abstract (sommario):

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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26

Nageshwaran, Sathiji, Heather C. Wilson, Anthony Dickenson e 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 Lambert–Eaton myasthenic syndrome (LEMS).

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27

Firth, Helen V., Jane A. Hurst e 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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28

Duchenne Muscular Dystrophy. CRC, 1996.

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29

Emery, Alan E. H. Duchenne muscular dystrophy. Oxford University Press, 1988.

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30

Muntoni, Francesco, Alan E. H. Emery e Rosaline C. M. Quinlivan. Duchenne Muscular Dystrophy. Oxford University Press, 2015.

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31

Chamberlain, Jeffrey S., e Thomas A. Rando, a cura di. Duchenne Muscular Dystrophy. CRC Press, 2006. http://dx.doi.org/10.3109/9780849374456.

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32

S, Chamberlain Jeffrey, e Rando Thomas A, a cura di. Duchenne muscular dystrophy: Advances in therapeutics. New York: Taylor & Francis, 2005.

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33

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

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34

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

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35

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

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36

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

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37

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

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38

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

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39

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

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40

Johnston, Ruth, Claire Tester, Joy Blakeney, Alex Howarth, Hether McAndrew, Nicola Traynor, Mary McCutcheon e Kate Stone. Occupational Therapy and Duchenne Muscular Dystrophy. Wiley, 2007.

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41

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

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42

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

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43

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

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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

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

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46

Duchenne muscular dystrophy: Animal models and genetic manipulation. New York: Raven Press, 1992.

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47

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

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48

Emery, Alan E. H., e 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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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 e Lianne Abbot. Guide to Duchenne Muscular Dystrophy: Information and Advice for Teachers and Parents. Kingsley Publishers, Jessica, 2017.

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