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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2003-8-12
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pubmed:abstractText |
According to widely used criteria (Bohan and Peter criteria, 1975), dermatomyositis (DM) is differentiated from polymyositis (PM) only by skin changes. More recent criteria also include histopathologic characteristics enabling the distinction between PM and DM and the differentiation of sporadic inclusion body myositis (s-IBM) from PM. The authors investigated the applicability of diagnostic features for diagnosing PM and DM.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1526-632X
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:day |
12
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pubmed:volume |
61
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
316-21
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:12913190-Adult,
pubmed-meshheading:12913190-Aged,
pubmed-meshheading:12913190-Biopsy,
pubmed-meshheading:12913190-Connective Tissue Diseases,
pubmed-meshheading:12913190-Dermatomyositis,
pubmed-meshheading:12913190-Diagnosis, Differential,
pubmed-meshheading:12913190-Female,
pubmed-meshheading:12913190-Follow-Up Studies,
pubmed-meshheading:12913190-Humans,
pubmed-meshheading:12913190-Male,
pubmed-meshheading:12913190-Middle Aged,
pubmed-meshheading:12913190-Muscle Weakness,
pubmed-meshheading:12913190-Muscular Dystrophies,
pubmed-meshheading:12913190-Myositis,
pubmed-meshheading:12913190-Myositis, Inclusion Body,
pubmed-meshheading:12913190-Polymyositis,
pubmed-meshheading:12913190-Retrospective Studies
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pubmed:year |
2003
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pubmed:articleTitle |
Polymyositis: an overdiagnosed entity.
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pubmed:affiliation |
Rudolf Magnus Institute of Neuroscience, Department of Neurology, University Medical Center, Utrecht, The Netherlands. M.F.G.vdMeulen@neuro.azu.nl
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pubmed:publicationType |
Journal Article
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