Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2010-5-12
pubmed:abstractText
Fabry's disease is an X-linked lysosomal storage disease caused by deficiency of alpha-galactosidase A enzyme activity. Decreased enzyme activity leads to accumulation of glycosphingolipid in different tissues, including endothelial and smooth-muscle cells and cardiomyocytes.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0001-5385
pubmed:author
pubmed:issnType
Print
pubmed:volume
65
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
185-92
pubmed:meshHeading
pubmed-meshheading:20458826-Adult, pubmed-meshheading:20458826-Aged, pubmed-meshheading:20458826-Biological Markers, pubmed-meshheading:20458826-Diagnosis, Differential, pubmed-meshheading:20458826-Echocardiography, pubmed-meshheading:20458826-Electrocardiography, pubmed-meshheading:20458826-Exercise Test, pubmed-meshheading:20458826-Exercise Tolerance, pubmed-meshheading:20458826-Fabry Disease, pubmed-meshheading:20458826-Female, pubmed-meshheading:20458826-Forced Expiratory Volume, pubmed-meshheading:20458826-Humans, pubmed-meshheading:20458826-Hypertrophy, Left Ventricular, pubmed-meshheading:20458826-Lung, pubmed-meshheading:20458826-Magnetic Resonance Imaging, pubmed-meshheading:20458826-Male, pubmed-meshheading:20458826-Middle Aged, pubmed-meshheading:20458826-Oxygen Consumption, pubmed-meshheading:20458826-Severity of Illness Index, pubmed-meshheading:20458826-Spirometry, pubmed-meshheading:20458826-Tomography, X-Ray Computed, pubmed-meshheading:20458826-Vital Capacity, pubmed-meshheading:20458826-alpha-Galactosidase
pubmed:year
2010
pubmed:articleTitle
Cardiopulmonary involvement in Fabry's disease.
pubmed:affiliation
Dept. of Clinical Physiology and Nuclear Medicine, Turku University Hospital, Finland. juhkos@utu.fi
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't