Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2010-2-10
pubmed:abstractText
Lipid-storage myopathy (LSM), defined by triglyceride accumulation in muscle fibres, is a heterogeneous group of lipid metabolic disorders predominantly affecting skeletal muscle. In the past 15 years, more than 200 cases of LSM have been reported in the Chinese literature, but the accurate pathogenic mechanisms are still unknown.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1468-330X
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
81
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
231-6
pubmed:meshHeading
pubmed-meshheading:19758981-Adolescent, pubmed-meshheading:19758981-Adult, pubmed-meshheading:19758981-Blotting, Western, pubmed-meshheading:19758981-Child, pubmed-meshheading:19758981-Electron-Transferring Flavoproteins, pubmed-meshheading:19758981-Female, pubmed-meshheading:19758981-Humans, pubmed-meshheading:19758981-Iron-Sulfur Proteins, pubmed-meshheading:19758981-Lipase, pubmed-meshheading:19758981-Lipid Metabolism Disorders, pubmed-meshheading:19758981-Male, pubmed-meshheading:19758981-Middle Aged, pubmed-meshheading:19758981-Multiple Acyl Coenzyme A Dehydrogenase Deficiency, pubmed-meshheading:19758981-Muscle, Skeletal, pubmed-meshheading:19758981-Muscle Weakness, pubmed-meshheading:19758981-Muscular Diseases, pubmed-meshheading:19758981-Oxidoreductases Acting on CH-NH Group Donors, pubmed-meshheading:19758981-Point Mutation, pubmed-meshheading:19758981-Riboflavin, pubmed-meshheading:19758981-Young Adult
pubmed:year
2010
pubmed:articleTitle
Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations.
pubmed:affiliation
Laboratory of Neuromuscular Disorders and Department of Neurology, Qilu Hospital, Shandong University, Jinan, PR China.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't