19602163

Source:http://linkedlifedata.com/resource/pubmed/id/19602163

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0023976, umls-concept:C1631597
pubmed:dateCreated	2009-7-15
pubmed:abstractText	Thanks to the contribution of molecular genetics, the genetic bases, the pathogenesis and genotype-phenotype correlation of diseases such as the long QT syndrome and catecholaminergic polymorphic ventricular tachycardia have been progressively unveiled and show an extremely high degree of genetic heterogeneity. Data from clinical registries are summarized together with the recommendations provided in clinical practice guidelines for management of patients with these diseases. Furthermore the evidence supporting the importance of genetic analysis for risk stratification and therapy selections is reviewed.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7803944
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	1540-8159
pubmed:author	pubmed-author:MonteforteNicolaN, pubmed-author:PrioriSilvia GSG
pubmed:issnType	Electronic
pubmed:volume	32 Suppl 2
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	S52-7
pubmed:meshHeading	pubmed-meshheading:19602163-Genetic Predisposition to Disease, pubmed-meshheading:19602163-Genetic Testing, pubmed-meshheading:19602163-Humans, pubmed-meshheading:19602163-Long QT Syndrome, pubmed-meshheading:19602163-Tachycardia, Ventricular
pubmed:year	2009
pubmed:articleTitle	The long QT syndrome and catecholaminergic polymorphic ventricular tachycardia.
pubmed:affiliation	Molecular Cardiology Fondazione Salvatore Maugeri, Pavia, Italy.
pubmed:publicationType	Journal Article, Review