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Books on the topic 'Dystrophie musculaire de Becker'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Consult the top 18 books for your research on the topic 'Dystrophie musculaire de Becker.'

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1

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

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2

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

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3

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

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4

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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5

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

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6

Jean-Guy, Bégin, ed. Einstein, chien-guide? Saint-Alphonse-de-Granby, Québec: Éditions de la Paix, 2006.

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7

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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8

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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9

Cohen, Jeffrey A., Justin J. Mowchun, Victoria H. Lawson, and Nathaniel M. Robbins. An 18-Year-Old Male with Slowly Progressive Weakness. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190491901.003.0028.

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Slow progression of proximal weakness in an adult may suggest Becker muscular dystrophy, but limb-girdle muscular dystrophy needs to be considered. This chapter discusses a diagnostic approach that includes the utility of ever-evolving genetic tests. Electromyography is helpful in cases of suspected muscular dystrophy without a family history, if creatine kinase levels are low, or in evaluation of possible female carriers for BMD who are symptomatic. Management considerations are also outlined. A muscular dystrophy clinic with a multidisciplinary approach is helpful for coordination of care. A consult from a clinical geneticist is often very helpful.

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10

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

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11

Partridge, Terence. Molecular and Cell Biology of Muscular Dystrophy. Springer, 2012.

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12

The Boys: Or, Waiting for the Electrician's Daughter. Gaspereau Press, 2005.

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13

Shannon, Joyce Brennfleck. Muscular Dystrophy Sourcebook: Basic Consumer Health Information About Congenital, Childhood-Onset, and Adult-Onset Forms of Muscular Dystrophy, Such as ... Becker, Emery-Drei (Health Reference Series). Omnigraphics, 2004.

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14

Two cases of early atrophy of muscles in cerebral disease. [S.l: s.n., 1985.

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15

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

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16

(Editor), Robert C. Griggs, and George Karpati (Editor), eds. Myoblast Transfer Therapy (Advances in Experimental Medicine and Biology). Springer, 1990.

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17

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

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18

Katherine M.D. Bushby (Editor) and Louise V.B. Anderson (Editor), eds. Muscular Dystrophy: Methods and Protocols (Methods in Molecular Medicine). Humana Press, 2001.

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