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  Fast and efficient free induction decay MRSI at 9.4 T: assessment of neuronal activation-related changes in the human brain biochemistry

Chadzynski, G., Bause, J., Shajan, G., Pohmann, R., Scheffler, K., & Ehses, P. (2016). Fast and efficient free induction decay MRSI at 9.4 T: assessment of neuronal activation-related changes in the human brain biochemistry. Poster presented at 24th Annual Meeting and Exhibition of the International Society for Magnetic Resonance in Medicine (ISMRM 2016), Singapore.

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Chadzynski, GL1, Autor           
Bause, J1, 2, Autor           
Shajan, G1, Autor           
Pohmann, R1, 2, Autor           
Scheffler, K1, 2, Autor           
Ehses, P1, Autor           
Affiliations:
1Department High-Field Magnetic Resonance, Max Planck Institute for Biological Cybernetics, Max Planck Society, ou_1497796              
2Max Planck Institute for Biological Cybernetics, Max Planck Society, ou_1497794              

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 Zusammenfassung: The aim was to design a MRSI-FID sequence for ultra-high field applications with high acquisition speed and sampling efficiency. The sequence allows acquisition of a 32×32 voxel matrix within approximately 2 min, down to 30 sec using parallel imaging. We have examined the suitability of this approach for assessing biochemical changes in the human visual cortex during a visual stimulus. Obtained results were in accordance with other functional MRS studies and indicate that the developed sequence is suitable for rapid monitoring of stimulus evoked changes in human brain biochemistry at a very high spatial resolution.

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 Datum: 2016-05-11
 Publikationsstatus: Erschienen
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 Identifikatoren: BibTex Citekey: ChadzynskiBSPSE2016
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Titel: 24th Annual Meeting and Exhibition of the International Society for Magnetic Resonance in Medicine (ISMRM 2016)
Veranstaltungsort: Singapore
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Titel: 24th Annual Meeting and Exhibition of the International Society for Magnetic Resonance in Medicine (ISMRM 2016)
Genre der Quelle: Konferenzband
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Seiten: - Band / Heft: - Artikelnummer: 2359 Start- / Endseite: - Identifikator: -