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Prospective motion correction with NMR markers using only native sequence elements.
Aranovitch, Alexander; Haeberlin, Maximilian; Gross, Simon; Dietrich, Benjamin E; Wilm, Bertram J; Brunner, David O; Schmid, Thomas; Luechinger, Roger; Pruessmann, Klaas P.
Afiliação
  • Aranovitch A; Institute for Biomedical Engineering, ETH Zurich and University of Zurich, Zurich, Switzerland.
  • Haeberlin M; Institute for Biomedical Engineering, ETH Zurich and University of Zurich, Zurich, Switzerland.
  • Gross S; Institute for Biomedical Engineering, ETH Zurich and University of Zurich, Zurich, Switzerland.
  • Dietrich BE; Institute for Biomedical Engineering, ETH Zurich and University of Zurich, Zurich, Switzerland.
  • Wilm BJ; Institute for Biomedical Engineering, ETH Zurich and University of Zurich, Zurich, Switzerland.
  • Brunner DO; Institute for Biomedical Engineering, ETH Zurich and University of Zurich, Zurich, Switzerland.
  • Schmid T; Institute for Biomedical Engineering, ETH Zurich and University of Zurich, Zurich, Switzerland.
  • Luechinger R; Institute for Biomedical Engineering, ETH Zurich and University of Zurich, Zurich, Switzerland.
  • Pruessmann KP; Institute for Biomedical Engineering, ETH Zurich and University of Zurich, Zurich, Switzerland.
Magn Reson Med ; 79(4): 2046-2056, 2018 04.
Article em En | MEDLINE | ID: mdl-28840611
PURPOSE: To develop a method of tracking active NMR markers that requires no alterations of common imaging sequences and can be used for prospective motion correction (PMC) in brain MRI. METHODS: Localization of NMR markers is achieved by acquiring short signal snippets in rapid succession and evaluating them jointly. To spatially encode the markers, snippets are timed such that signal phase is accrued during sequence intervals with suitably diverse gradient actuation. For motion tracking and PMC in brain imaging, the markers are mounted on a lightweight headset. PMC is then demonstrated with high-resolution T2 *- and T1 -weighted imaging sequences in the presence of instructed as well as residual unintentional head motion. RESULTS: With both unaltered sequences, motion tracking was achieved with precisions on the order of 10 µm and 0.01° and temporal resolution of 48 and 39 ms, respectively. On this basis, PMC improved image quality significantly throughout. CONCLUSION: The proposed approach permits high-precision motion tracking and PMC with standard imaging sequences. It does so without altering sequence design and thus overcomes a key hindrance to routine motion tracking with NMR markers. Magn Reson Med 79:2046-2057, 2018. © 2017 International Society for Magnetic Resonance in Medicine.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Imageamento por Ressonância Magnética / Espectroscopia de Ressonância Magnética / Cabeça Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Imageamento por Ressonância Magnética / Espectroscopia de Ressonância Magnética / Cabeça Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article