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19097109
Source:
http://linkedlifedata.com/resource/pubmed/id/19097109
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Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0024487
,
umls-concept:C0026882
,
umls-concept:C0242692
,
umls-concept:C0342289
,
umls-concept:C0521451
,
umls-concept:C1742737
pubmed:issue
1
pubmed:dateCreated
2008-12-24
pubmed:abstractText
To investigate high-energy phosphate metabolism in striated skeletal muscle of patients with Maternally Inherited Diabetes and Deafness (MIDD) syndrome.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9105850
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Phosphorus
,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphorus Isotopes
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1053-1807
pubmed:author
pubmed-author:DoornbosJoostJ
,
pubmed-author:LemkesHerman H P JHH
,
pubmed-author:MaassenJ AntonieJA
,
pubmed-author:SmitJan W AJW
,
pubmed-author:de RoosAlbertA
,
pubmed-author:van ElderenSaskia G CSG
,
pubmed-author:van EssenEinar H REH
pubmed:issnType
Print
pubmed:volume
29
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
127-31
pubmed:meshHeading
pubmed-meshheading:19097109-Adult
,
pubmed-meshheading:19097109-Deafness
,
pubmed-meshheading:19097109-Diabetes Mellitus
,
pubmed-meshheading:19097109-Female
,
pubmed-meshheading:19097109-Genetic Predisposition to Disease
,
pubmed-meshheading:19097109-Heterozygote
,
pubmed-meshheading:19097109-Humans
,
pubmed-meshheading:19097109-Magnetic Resonance Spectroscopy
,
pubmed-meshheading:19097109-Male
,
pubmed-meshheading:19097109-Mitochondria, Muscle
,
pubmed-meshheading:19097109-Mitochondrial Diseases
,
pubmed-meshheading:19097109-Mothers
,
pubmed-meshheading:19097109-Muscle, Skeletal
,
pubmed-meshheading:19097109-Mutation
,
pubmed-meshheading:19097109-Phosphorus
,
pubmed-meshheading:19097109-Phosphorus Isotopes
pubmed:year
2009
pubmed:articleTitle
Phosphorus-31 magnetic resonance spectroscopy of skeletal muscle in maternally inherited diabetes and deafness A3243G mitochondrial mutation carriers.
pubmed:affiliation
Department of Radiology, Leiden University Medical Centre, Leiden, The Netherlands. s.g.c.van_elderen@lumc.nl
pubmed:publicationType
Journal Article