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Acquired Myopathy/Dystrophies
dc.contributor.authorChiodo, Anthony
dc.date.accessioned2019-01-15T20:29:37Z
dc.date.available2019-01-15T20:29:37Z
dc.date.issued2013-05
dc.identifier.citationChiodo, Anthony (2013). "Acquired Myopathy/Dystrophies." PM&R 5: S74-S80.
dc.identifier.issn1934-1482
dc.identifier.issn1934-1563
dc.identifier.urihttps://hdl.handle.net/2027.42/147092
dc.description.abstractDiseases of muscle may be congenital or acquired. They cause muscle weakness without sensory loss. The onset, distribution, and clinical course help to differentiate the type of muscle disorder. The diagnostic workup may include laboratory examination, electrodiagnostic studies, and muscle biopsy. A definitive diagnosis leads to better decision making with regard to treatment, genetic education, prognosis, functional expectations, and the impact of exercise on muscle function.
dc.publisherWiley Periodicals, Inc.
dc.titleAcquired Myopathy/Dystrophies
dc.typeArticleen_US
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelKinesiology and Sports
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.contributor.affiliationumPhysical Medicine and Rehabilitation, University of Michigan Hospital, 325 E Eisenhower Parkway, Ann Arbor, MI 48118
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/147092/1/pmr2s74.pdf
dc.identifier.doi10.1016/j.pmrj.2013.04.004
dc.identifier.sourcePM&R
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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