19194511

Source:http://linkedlifedata.com/resource/pubmed/id/19194511

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0013264, umls-concept:C0243161, umls-concept:C0681890, umls-concept:C1517942, umls-concept:C1704788, umls-concept:C1850620
pubmed:issue	2
pubmed:dateCreated	2009-2-5
pubmed:abstractText	To explore clinical heterogeneity of Duchenne muscular dystrophy (DMD), viewed as a major obstacle to the interpretation of therapeutic trials
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-10463847, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-10477238, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-10797032, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-11859054, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-12849184, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-14600829, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-14636778, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-14678803, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-14975083, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-14995084, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-1528016, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-1552307, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-1570841, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-15766818, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-15818650, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-15984021, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-16969838, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-17041906, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-17490881, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-2927672, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-3115236, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-6343858, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-7247762, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-7890131, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-8239956, http://linkedlifedata.com/resource/pubmed/commentcorrection/19194511-8411067
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101285081
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	1932-6203
pubmed:author	pubmed-author:Bastuji-GarinSylvieS, pubmed-author:BecaneHenri-MarcHM, pubmed-author:ChellyJamelJ, pubmed-author:ChironCatherineC, pubmed-author:ChristovChristoC, pubmed-author:DesguerreIsabelleI, pubmed-author:GherardiRomain KRK, pubmed-author:LeturcqFranceF, pubmed-author:MayerMicheleM, pubmed-author:ZellerReinhardR
pubmed:issnType	Electronic
pubmed:volume	4
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	e4347
pubmed:dateRevised	2009-11-18
pubmed:meshHeading	pubmed-meshheading:19194511-Adolescent, pubmed-meshheading:19194511-Child, pubmed-meshheading:19194511-Cluster Analysis, pubmed-meshheading:19194511-Female, pubmed-meshheading:19194511-Follow-Up Studies, pubmed-meshheading:19194511-Genetic Heterogeneity, pubmed-meshheading:19194511-Genotype, pubmed-meshheading:19194511-Heart Function Tests, pubmed-meshheading:19194511-Humans, pubmed-meshheading:19194511-Male, pubmed-meshheading:19194511-Muscle Strength, pubmed-meshheading:19194511-Muscular Dystrophy, Duchenne, pubmed-meshheading:19194511-Phenotype, pubmed-meshheading:19194511-Principal Component Analysis, pubmed-meshheading:19194511-Respiratory Function Tests, pubmed-meshheading:19194511-Time Factors
pubmed:year	2009
pubmed:articleTitle	Clinical heterogeneity of duchenne muscular dystrophy (DMD): definition of sub-phenotypes and predictive criteria by long-term follow-up.
pubmed:affiliation	Department of Neuropediatrics, Neuromuscular Disease Reference Center Garches-Necker-Mondor-Hendaye, Necker-Enfants Malades Hospital, Paris, France.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't