| pubmed-article:7949679 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:7949679 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
| pubmed-article:7949679 | lifeskim:mentions | umls-concept:C0011923 | lld:lifeskim |
| pubmed-article:7949679 | lifeskim:mentions | umls-concept:C0006104 | lld:lifeskim |
| pubmed-article:7949679 | lifeskim:mentions | umls-concept:C0205307 | lld:lifeskim |
| pubmed-article:7949679 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
| pubmed-article:7949679 | lifeskim:mentions | umls-concept:C1514863 | lld:lifeskim |
| pubmed-article:7949679 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:7949679 | pubmed:dateCreated | 1994-11-30 | lld:pubmed |
| pubmed-article:7949679 | pubmed:abstractText | Studies have been performed to evaluate the reproducibility of longitudinal acquisitions with short TE spectroscopic magnetic resonance (MR) imaging of human brain. In healthy volunteers, the ratios of N-acetyl-aspartate (NAA) and choline (Cho) with respect to total creatine (Cr) (creatine and phosphocreatine) have been examined in terms of voxel-to-voxel, acquisition-to-acquisition, and subject-to-subject variation. Overall coefficients of variation for NAA/Cr ratios and Cho/Cr ratios were 18% and 16%, respectively. The interacquisition variation was not statistically significant (P = .05) for either ratio. In terms of F ratios, the dominant source of variation in the NAA/Cr ratio was intersubject variability, whereas for the Cho/Cr ratio the dominant source of variation was intervoxel variability. Consequences of spectroscopic processing with spatial apodization and postacquisition water suppression and resolution enhancement were also examined. Such reproducibility studies are crucial if longitudinal spectroscopic evaluations are to be performed in a clinical setting to follow the natural course of disease states or the effects of therapy. | lld:pubmed |
| pubmed-article:7949679 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7949679 | pubmed:language | eng | lld:pubmed |
| pubmed-article:7949679 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7949679 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:7949679 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7949679 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7949679 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:7949679 | pubmed:issn | 1053-1807 | lld:pubmed |
| pubmed-article:7949679 | pubmed:author | pubmed-author:WolinskyJ SJS | lld:pubmed |
| pubmed-article:7949679 | pubmed:author | pubmed-author:DoyleT JTJ | lld:pubmed |
| pubmed-article:7949679 | pubmed:author | pubmed-author:JacksonE FEF | lld:pubmed |
| pubmed-article:7949679 | pubmed:author | pubmed-author:NarayanaP APA | lld:pubmed |
| pubmed-article:7949679 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:7949679 | pubmed:volume | 4 | lld:pubmed |
| pubmed-article:7949679 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:7949679 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:7949679 | pubmed:pagination | 545-51 | lld:pubmed |
| pubmed-article:7949679 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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| pubmed-article:7949679 | pubmed:meshHeading | pubmed-meshheading:7949679-... | lld:pubmed |
| pubmed-article:7949679 | pubmed:articleTitle | Short TE hydrogen-1 spectroscopic MR imaging of normal human brain: reproducibility studies. | lld:pubmed |
| pubmed-article:7949679 | pubmed:affiliation | Department of Radiology, University of Texas Medical School, Houston. | lld:pubmed |
| pubmed-article:7949679 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:7949679 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:7949679 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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