19588393

Source:http://linkedlifedata.com/resource/pubmed/id/19588393

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0020179, umls-concept:C0087111, umls-concept:C0231220
pubmed:issue	3
pubmed:dateCreated	2009-7-9
pubmed:abstractText	Huntington's disease (HD) is an orphan autosomal dominant neurodegenerative disorder caused by the amplification of a nucleic acids triplet repeat. It is characterised by core symptoms of chorea, progressive dementia and psychiatric manifestations such as depression, irritability, apathy and psychosis. In current clinical practice, drugs exist that seem to improve symptoms for HD patients. However, their effectiveness has not been fully measured.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100909747
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	1469-493X
pubmed:author	pubmed-author:CoelhoMiguel MMM, pubmed-author:FerreiraJoaquimJ, pubmed-author:MestreTiagoT, pubmed-author:RosaMárioM, pubmed-author:SampaioCristinaC
pubmed:issnType	Electronic
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	CD006456
pubmed:meshHeading	pubmed-meshheading:19588393-Chorea, pubmed-meshheading:19588393-Humans, pubmed-meshheading:19588393-Huntington Disease, pubmed-meshheading:19588393-Randomized Controlled Trials as Topic
pubmed:year	2009
pubmed:articleTitle	Therapeutic interventions for symptomatic treatment in Huntington's disease.
pubmed:affiliation	Neurological Clinical Research Unit, Institute of Molecular Medicine, Hospital de Santa Maria, Av. Prof. Egas Moniz, Lisboa, Portugal, 1649-028.
pubmed:publicationType	Journal Article, Review, Meta-Analysis