| pubmed-article:19893767 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19893767 | lifeskim:mentions | umls-concept:C0007193 | lld:lifeskim |
| pubmed-article:19893767 | lifeskim:mentions | umls-concept:C0009226 | lld:lifeskim |
| pubmed-article:19893767 | lifeskim:mentions | umls-concept:C0024188 | lld:lifeskim |
| pubmed-article:19893767 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:19893767 | lifeskim:mentions | umls-concept:C0011155 | lld:lifeskim |
| pubmed-article:19893767 | lifeskim:mentions | umls-concept:C1533148 | lld:lifeskim |
| pubmed-article:19893767 | lifeskim:mentions | umls-concept:C0047420 | lld:lifeskim |
| pubmed-article:19893767 | pubmed:dateCreated | 2009-11-6 | lld:pubmed |
| pubmed-article:19893767 | pubmed:abstractText | 3-hydroxy-3-methylglutaryl-coenzyme A (HMG CoA) lyase deficiency is an inborn error of metabolism characterized by impairment of ketogenesis and leucine catabolism resulting in an organic acidopathy. In 1994, a case of dilated cardiomyopathy and fatal arrhythmia was reported in a 7-month-old infant. We report a case of dilated cardiomyopathy in association with HMG CoA lyase deficiency in a 23-year-old man with the acute presentation of heart failure. To our knowledge, this is the first case reported in an adult. | lld:pubmed |
| pubmed-article:19893767 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19893767 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19893767 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19893767 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19893767 | pubmed:language | eng | lld:pubmed |
| pubmed-article:19893767 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19893767 | pubmed:status | PubMed-not-MEDLINE | lld:pubmed |
| pubmed-article:19893767 | pubmed:issn | 1687-9627 | lld:pubmed |
| pubmed-article:19893767 | pubmed:author | pubmed-author:LeungAlexande... | lld:pubmed |
| pubmed-article:19893767 | pubmed:author | pubmed-author:EzekowitzJust... | lld:pubmed |
| pubmed-article:19893767 | pubmed:author | pubmed-author:LeungAlexande... | lld:pubmed |
| pubmed-article:19893767 | pubmed:author | pubmed-author:ChanAlicia... | lld:pubmed |
| pubmed-article:19893767 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:19893767 | pubmed:volume | 2009 | lld:pubmed |
| pubmed-article:19893767 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19893767 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19893767 | pubmed:pagination | 183125 | lld:pubmed |
| pubmed-article:19893767 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19893767 | pubmed:articleTitle | A Case of Dilated Cardiomyopathy Associated with 3-Hydroxy-3-Methylglutaryl-Coenzyme A (HMG CoA) Lyase Deficiency. | lld:pubmed |
| pubmed-article:19893767 | pubmed:affiliation | Department of Medicine, University of Alberta Hospital, University of Alberta, Edmonton, AB, Canada T6G 2B7. | lld:pubmed |
| pubmed-article:19893767 | pubmed:publicationType | Journal Article | lld:pubmed |
