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dc.creatorKousi, E.en
dc.creatorTsougos, I.en
dc.creatorKapsalaki, E.en
dc.creatorKappas, C.en
dc.creatorTheodorou, K.en
dc.date.accessioned2015-11-23T10:36:28Z
dc.date.available2015-11-23T10:36:28Z
dc.date.issued2009
dc.identifier10.1007/978-3-642-03879-2-95
dc.identifier.isbn9783642038785
dc.identifier.issn16800737
dc.identifier.urihttp://hdl.handle.net/11615/29886
dc.description.abstractBrain MR imaging at 3T has been increasingly used in clinical practice since a great deal of effort has been invested in research into high magnetic fields to overcome the difficulties of successively working with stronger fields. Theoretically the signal to noise ratio (SNR) of a 3T MR scanner will be double that of a 1.5T one which is advantageous for MR spectroscopy as this technique has always required the strongest possible magnetic field strength. However, the relationship between the magnetic field used and the spectra obtained is very complex depended on several other data acquisition parameters not only field strength. Single-voxel at short echo time (TE=35msec) and multivoxel at long echo time (TE=144msec) spectra were recorded for 46 patients with several brain lesions using PRESS pulse sequence. Spectra were compared in terms of resolution as it varies among changes of data acquisition parameters such as NEX (Number of Excitations), NSA (Number of Signals Averaging) and field homogeneity. Spectra exhibited significantly improved resolution as field homogeneity was improved and NEX as well as NSA were increased. MRS metabolic profiles at 3T gave valuable clinical information when differentiating among brain lesions and tumour stages. However, in some cases, differences among tumour grade and lesion type were subtle, rendering tumour classification a difficult issue. © 2009 Springer-Verlag.en
dc.source.urihttp://www.scopus.com/inward/record.url?eid=2-s2.0-77950903238&partnerID=40&md5=c05e635cba40471b4cbf08f7e6e1fffe
dc.subject3Ten
dc.subjectBrain lesionsen
dc.subjectMetabolic profileen
dc.subjectMRSen
dc.subjectAcquisition parametersen
dc.subjectBrain MRen
dc.subjectClinical informationen
dc.subjectClinical practicesen
dc.subjectEcho timeen
dc.subjectField homogeneityen
dc.subjectField strengthsen
dc.subjectHigh magnetic fieldsen
dc.subjectHuman brainen
dc.subjectMagnetic field strengthsen
dc.subjectMetabolic profilesen
dc.subjectMR scannersen
dc.subjectMR spectroscopyen
dc.subjectProton magnetic resonance spectroscopiesen
dc.subjectPulse sequenceen
dc.subjectTumour gradeen
dc.subjectBiomedical engineeringen
dc.subjectMagnetic field effectsen
dc.subjectMagnetic resonance imagingen
dc.subjectMedical imagingen
dc.subjectMetabolismen
dc.subjectNuclear magnetic resonance spectroscopyen
dc.subjectPhysicsen
dc.subjectProtonsen
dc.subjectSignal to noise ratioen
dc.subjectSpectroscopyen
dc.subjectTumorsen
dc.subjectMagnetic resonanceen
dc.titleProton magnetic resonance spectroscopy at 3T - Evaluation of metabolic profile of human brain lesionsen
dc.typeconferenceItemen


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