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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2011-1-25
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pubmed:abstractText |
There are currently no effective treatments to halt the muscle breakdown in Duchenne muscular dystrophy (DMD), although genetic-based clinical trials are being piloted. Most of these trials have as an endpoint the restoration of dystrophin in muscle fibers, hence requiring sufficiently well-preserved muscle of recruited patients. The choice of the muscles to be studied and the role of noninvasive methods to assess muscle preservation therefore require further evaluation.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-10028989,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-11030068,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-12145248,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-12401454,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-1300186,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-15451904,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-16497502,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-17260395,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-17885450,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-17952895,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-18094282,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-18160687,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-18207401,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-19139297,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-19713152,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-1994993,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-2268764,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-2743685,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-3484872,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-3684364,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21263136-8421754
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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 |
Jan
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pubmed:issn |
1526-632X
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pubmed:author |
pubmed-author:Arechavala-GomezaVV,
pubmed-author:BushbyKK,
pubmed-author:CirakSS,
pubmed-author:FengLL,
pubmed-author:GloverAA,
pubmed-author:GosalakkalJ AJA,
pubmed-author:GuglieriMM,
pubmed-author:HollingsworthK GKG,
pubmed-author:Hughes-CarreLL,
pubmed-author:HuntDD,
pubmed-author:JayawantSS,
pubmed-author:JungbluthHH,
pubmed-author:KinaliMM,
pubmed-author:ManzurA YAY,
pubmed-author:MercuriEE,
pubmed-author:MorganJ EJE,
pubmed-author:MuntoniFF,
pubmed-author:NadeauAA,
pubmed-author:QuinlivanR MRM,
pubmed-author:RoperH PHP,
pubmed-author:RutherfordMM,
pubmed-author:SewryCC,
pubmed-author:StraubVV
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pubmed:issnType |
Electronic
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pubmed:day |
25
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pubmed:volume |
76
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
346-53
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pubmed:dateRevised |
2011-8-1
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pubmed:meshHeading |
pubmed-meshheading:21263136-Adolescent,
pubmed-meshheading:21263136-Child,
pubmed-meshheading:21263136-Foot,
pubmed-meshheading:21263136-Humans,
pubmed-meshheading:21263136-Leg,
pubmed-meshheading:21263136-Magnetic Resonance Imaging,
pubmed-meshheading:21263136-Male,
pubmed-meshheading:21263136-Muscle, Skeletal,
pubmed-meshheading:21263136-Muscular Dystrophy, Duchenne
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pubmed:year |
2011
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pubmed:articleTitle |
Muscle histology vs MRI in Duchenne muscular dystrophy.
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pubmed:affiliation |
The Dubowitz Neuromuscular Centre, Institute of Child Health, London, UK.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't,
Multicenter Study
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