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Libros sobre el tema "Dystrophin"

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

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1

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

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2

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

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3

D'Souza, Vinita N. Dystrophin expression in the retina. National Library of Canada, 1995.

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4

Bestard, Jennifer. Dystrophin gene regulation in muscle. National Library of Canada, 2000.

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5

Thanh, Le Thiet. Exon-specific monoclonal antibodies against dystrophin. University of Salford, 1995.

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6

Dally, Ghassan Y. Characterization of nommuscle isoforms of dystrophin. National Library of Canada, 1996.

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7

Cisternas, Felipe A. The function of alternatively spliced isoforms of dystrophin. National Library of Canada, 2000.

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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

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

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10

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

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11

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

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12

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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13

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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14

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

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15

Querques, Giuseppe, and Eric H. Souied, eds. Macular Dystrophies. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-26621-3.

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16

I, Charash Leon, ed. Muscular dystrophy and other neuromuscular diseases: Psychosocial issues. Haworth Press, 1991.

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17

1934-, Ozawa Eijirō, Masaki Tomoh, and Nabeshima Yoichi, eds. Frontiers in muscle research: Myogenesis, muscle contraction, and muscle dystrophy : proceedings of the Uehara Memorial Foundation Symposium on Frontiers in Muscle Research, Tokyo, 15-19 July 1990. Excerpta Medica, 1991.

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18

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

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19

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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20

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

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21

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

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22

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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23

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

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24

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

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25

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

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26

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

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27

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

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28

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

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29

Charles, Emerson, Hoffmann-La Roche inc, and University of California, Los Angeles., eds. Molecular biology of muscle development: Proceedings of a Roche-UCLA Symposium, held in Park City, Utah, March 15-22, 1985. A.R. Liss, 1986.

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30

Puech, Bernard, Jean-Jacques De Laey, and Graham E. Holder, eds. Inherited Chorioretinal Dystrophies. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-540-69466-3.

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31

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

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32

Myrianthopoulos, Ntinos C. (Ntinos Cleovoulou), Vayenas Constantina, and Dixon Joanne, eds. Dystrophia myotonica and related disorders. 2nd ed. Dr. J.E. Caughey, 1991.

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33

Molecular mechanisms of muscular dystrophies. Landes Bioscience, 2005.

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34

Kaplan, Tamara, and Tracey Milligan. Myopathy (DRAFT). Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190650261.003.0017.

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The video in this chapter discusses myopathy, including its symptoms (pain, stiffness, cramps, exertional fatigue, myoglobinuria, shortness of breath, rash), muscular dystrophy and dystrophinopathies (Becker with reduced dystrophin and Duchenne with no dystrophin), polymyositis, dermatomyositis, and inclusion body myositis.
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35

Howard, Perry Leigh. The functional diversity of dystrophin. 1999.

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36

(Foreword), Marlin Bobrow, Susan C. Brown (Editor), and Jack A. Lucy (Editor), eds. Dystrophin: Gene, Protein and Cell Biology. Cambridge University Press, 1997.

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37

Bulman, Dennis Edward. Characterization of dystrophin using region specific antisera. 1993.

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38

Ditta, Stephanie Doreen. Matrix attachment regions in the human dystrophin gene. 2000.

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39

Demacio, Paula Constance. Characterization of dystrophin protein complexes in the retina. 2001.

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40

Ferguson, Meghan MacRae. Characterization of alpha-catulin, a new dystrophin-associated protein. 2004.

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41

Tennyson, Christine Nathalice. Synthesis, splicing, and stability of dystrophin gene products in muscle. 1996.

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42

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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43

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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44

Perez, Antonio L. Systemic cell therapy for Duchenne muscular dystrophy: Progenitor cell-based restoration of dystrophin is enhanced by intra-arterial delivery and CXCR4 expression. 2010.

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45

Muscular dystrophy sourcebook: Basic consumer information about congenital, childhood-onset, and adult-onset forms of muscular dystrophy ... Omnigraphics, Inc., 2004.

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46

Muchenberger, Silke. Charakterisierung der Dystrophin-Expression bei myogenen und neuromuskulären Erkrankungen im Vergleich immunhistochemischer Ergebnisse zu Befunden im Westernblot. 1994.

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47

Emery, Alan E. H. Muscular Dystrophy: The Facts. Oxford University Press, USA, 1994.

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48

Emery, Alan E. H. Muscular Dystrophy: The Facts (Oxford Medical Publications). Oxford University Press, USA, 1994.

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49

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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50

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

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