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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2002-3-18
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pubmed:abstractText |
We investigated the prevalence of lamin A/C (LMNA) gene defects in familial and sporadic dilated cardiomyopathies (DCM) associated with atrioventricular block (AVB) or increased serum creatine-phosphokinase (sCPK), and the corresponding changes in myocardial and protein expression.
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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:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0735-1097
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pubmed:author |
pubmed-author:ArbustiniEloisaE,
pubmed-author:BaldiniElisaE,
pubmed-author:CampanaCarloC,
pubmed-author:DiegoliMartaM,
pubmed-author:GavazziAntonelloA,
pubmed-author:GrassoMauriziaM,
pubmed-author:NegriAndreaA,
pubmed-author:PilottoAndreaA,
pubmed-author:RepettoAlessandraA,
pubmed-author:ScelsiLauraL,
pubmed-author:TavazziLuigiL
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pubmed:issnType |
Print
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pubmed:day |
20
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pubmed:volume |
39
|
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pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
981-90
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11897440-Adolescent,
pubmed-meshheading:11897440-Adult,
pubmed-meshheading:11897440-Age Factors,
pubmed-meshheading:11897440-Aged,
pubmed-meshheading:11897440-Cardiomyopathy, Dilated,
pubmed-meshheading:11897440-Child,
pubmed-meshheading:11897440-Child, Preschool,
pubmed-meshheading:11897440-Child Welfare,
pubmed-meshheading:11897440-Creatine Kinase,
pubmed-meshheading:11897440-Family Health,
pubmed-meshheading:11897440-Female,
pubmed-meshheading:11897440-Follow-Up Studies,
pubmed-meshheading:11897440-Genes, Dominant,
pubmed-meshheading:11897440-Heart Block,
pubmed-meshheading:11897440-Humans,
pubmed-meshheading:11897440-Lamin Type A,
pubmed-meshheading:11897440-Lamins,
pubmed-meshheading:11897440-Male,
pubmed-meshheading:11897440-Middle Aged,
pubmed-meshheading:11897440-Mutation,
pubmed-meshheading:11897440-Myocardium,
pubmed-meshheading:11897440-Nuclear Proteins,
pubmed-meshheading:11897440-Pedigree,
pubmed-meshheading:11897440-Phenotype,
pubmed-meshheading:11897440-Polymorphism, Genetic,
pubmed-meshheading:11897440-Predictive Value of Tests,
pubmed-meshheading:11897440-Prevalence
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pubmed:year |
2002
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pubmed:articleTitle |
Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease.
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pubmed:affiliation |
Molecular Diagnostic Division, IRCCS Policlinico San Matteo, Pavia, Italy. e.arbustini@smatteo.pv.it
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
|
