Loading…

Acquired Myopathy/Dystrophies

Diseases 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...

Full description

Saved in:
Bibliographic Details
Published in:PM & R 2013-05, Vol.5 (5), p.S74-S80
Main Author: Chiodo, Anthony, MD
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c5034-6ebc63d51a3432cf49fad7155bf563d18feeacf63907caba6693eede92e4686c3
cites cdi_FETCH-LOGICAL-c5034-6ebc63d51a3432cf49fad7155bf563d18feeacf63907caba6693eede92e4686c3
container_end_page S80
container_issue 5
container_start_page S74
container_title PM & R
container_volume 5
creator Chiodo, Anthony, MD
description Diseases 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.
doi_str_mv 10.1016/j.pmrj.2013.04.004
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1365050180</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S1934148213001731</els_id><sourcerecordid>1365050180</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5034-6ebc63d51a3432cf49fad7155bf563d18feeacf63907caba6693eede92e4686c3</originalsourceid><addsrcrecordid>eNqNkU9L5EAQxRtxUdf1CwiKx71MrEp3OgmIIK77D8VlXc9FT6eCHTOT2D1R8u3tMOrBg-yp6vDeq-L3hNhHSBBQHzdJv_BNkgLKBFQCoDbEDpZSzTDTcvN1V0W6LT6H0ABohYXeEtupzAqFGnbEwZl9GJzn6uhq7HqzuhuPv41h5bv-znH4Ij7Vpg289zJ3xe33i3_nP2eX1z9-nZ9dzmwG8YTmudWyytBIJVNbq7I2VY5ZNq_jIxUWNbOxtZYl5NbMjdalZK64TFnpQlu5K76uc3vfPQwcVrRwwXLbmiV3QyCUOoMMsIAoTddS67sQPNfUe7cwfiQEmrBQQxMWmrAQKIpYounwJX-YL7h6s7xyiIJ8LXhyLY__EUl_rv7-vsmn6JO1kyOfR8eegnW8tFxFqnZFVec-_uz0nd22bumsae955NB0g19G8oQUUgK6mSqdGkUJgLlE-Qy6Fpj2</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1365050180</pqid></control><display><type>article</type><title>Acquired Myopathy/Dystrophies</title><source>Wiley</source><creator>Chiodo, Anthony, MD</creator><creatorcontrib>Chiodo, Anthony, MD</creatorcontrib><description>Diseases 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.</description><identifier>ISSN: 1934-1482</identifier><identifier>EISSN: 1934-1563</identifier><identifier>DOI: 10.1016/j.pmrj.2013.04.004</identifier><identifier>PMID: 23584160</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Biopsy ; Diagnosis, Differential ; Electrodiagnosis - methods ; Humans ; Muscle Weakness - physiopathology ; Muscular Diseases - diagnosis ; Muscular Diseases - etiology ; Muscular Diseases - physiopathology ; Muscular Dystrophies - diagnosis ; Muscular Dystrophies - etiology ; Muscular Dystrophies - physiopathology ; Physical Medicine and Rehabilitation</subject><ispartof>PM &amp; R, 2013-05, Vol.5 (5), p.S74-S80</ispartof><rights>American Academy of Physical Medicine and Rehabilitation</rights><rights>2013 American Academy of Physical Medicine and Rehabilitation</rights><rights>2013 by the American Academy of Physical Medicine and Rehabilitation</rights><rights>Copyright © 2013 American Academy of Physical Medicine and Rehabilitation. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5034-6ebc63d51a3432cf49fad7155bf563d18feeacf63907caba6693eede92e4686c3</citedby><cites>FETCH-LOGICAL-c5034-6ebc63d51a3432cf49fad7155bf563d18feeacf63907caba6693eede92e4686c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23584160$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chiodo, Anthony, MD</creatorcontrib><title>Acquired Myopathy/Dystrophies</title><title>PM &amp; R</title><addtitle>PM R</addtitle><description>Diseases 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.</description><subject>Biopsy</subject><subject>Diagnosis, Differential</subject><subject>Electrodiagnosis - methods</subject><subject>Humans</subject><subject>Muscle Weakness - physiopathology</subject><subject>Muscular Diseases - diagnosis</subject><subject>Muscular Diseases - etiology</subject><subject>Muscular Diseases - physiopathology</subject><subject>Muscular Dystrophies - diagnosis</subject><subject>Muscular Dystrophies - etiology</subject><subject>Muscular Dystrophies - physiopathology</subject><subject>Physical Medicine and Rehabilitation</subject><issn>1934-1482</issn><issn>1934-1563</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqNkU9L5EAQxRtxUdf1CwiKx71MrEp3OgmIIK77D8VlXc9FT6eCHTOT2D1R8u3tMOrBg-yp6vDeq-L3hNhHSBBQHzdJv_BNkgLKBFQCoDbEDpZSzTDTcvN1V0W6LT6H0ABohYXeEtupzAqFGnbEwZl9GJzn6uhq7HqzuhuPv41h5bv-znH4Ij7Vpg289zJ3xe33i3_nP2eX1z9-nZ9dzmwG8YTmudWyytBIJVNbq7I2VY5ZNq_jIxUWNbOxtZYl5NbMjdalZK64TFnpQlu5K76uc3vfPQwcVrRwwXLbmiV3QyCUOoMMsIAoTddS67sQPNfUe7cwfiQEmrBQQxMWmrAQKIpYounwJX-YL7h6s7xyiIJ8LXhyLY__EUl_rv7-vsmn6JO1kyOfR8eegnW8tFxFqnZFVec-_uz0nd22bumsae955NB0g19G8oQUUgK6mSqdGkUJgLlE-Qy6Fpj2</recordid><startdate>201305</startdate><enddate>201305</enddate><creator>Chiodo, Anthony, MD</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201305</creationdate><title>Acquired Myopathy/Dystrophies</title><author>Chiodo, Anthony, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5034-6ebc63d51a3432cf49fad7155bf563d18feeacf63907caba6693eede92e4686c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Biopsy</topic><topic>Diagnosis, Differential</topic><topic>Electrodiagnosis - methods</topic><topic>Humans</topic><topic>Muscle Weakness - physiopathology</topic><topic>Muscular Diseases - diagnosis</topic><topic>Muscular Diseases - etiology</topic><topic>Muscular Diseases - physiopathology</topic><topic>Muscular Dystrophies - diagnosis</topic><topic>Muscular Dystrophies - etiology</topic><topic>Muscular Dystrophies - physiopathology</topic><topic>Physical Medicine and Rehabilitation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chiodo, Anthony, MD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>PM &amp; R</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chiodo, Anthony, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acquired Myopathy/Dystrophies</atitle><jtitle>PM &amp; R</jtitle><addtitle>PM R</addtitle><date>2013-05</date><risdate>2013</risdate><volume>5</volume><issue>5</issue><spage>S74</spage><epage>S80</epage><pages>S74-S80</pages><issn>1934-1482</issn><eissn>1934-1563</eissn><abstract>Diseases 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.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23584160</pmid><doi>10.1016/j.pmrj.2013.04.004</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1934-1482
ispartof PM & R, 2013-05, Vol.5 (5), p.S74-S80
issn 1934-1482
1934-1563
language eng
recordid cdi_proquest_miscellaneous_1365050180
source Wiley
subjects Biopsy
Diagnosis, Differential
Electrodiagnosis - methods
Humans
Muscle Weakness - physiopathology
Muscular Diseases - diagnosis
Muscular Diseases - etiology
Muscular Diseases - physiopathology
Muscular Dystrophies - diagnosis
Muscular Dystrophies - etiology
Muscular Dystrophies - physiopathology
Physical Medicine and Rehabilitation
title Acquired Myopathy/Dystrophies
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T16%3A18%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Acquired%20Myopathy/Dystrophies&rft.jtitle=PM%20&%20R&rft.au=Chiodo,%20Anthony,%20MD&rft.date=2013-05&rft.volume=5&rft.issue=5&rft.spage=S74&rft.epage=S80&rft.pages=S74-S80&rft.issn=1934-1482&rft.eissn=1934-1563&rft_id=info:doi/10.1016/j.pmrj.2013.04.004&rft_dat=%3Cproquest_cross%3E1365050180%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c5034-6ebc63d51a3432cf49fad7155bf563d18feeacf63907caba6693eede92e4686c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1365050180&rft_id=info:pmid/23584160&rfr_iscdi=true