MRI data were acquired on a Siemens 3T MAGNETOM PrismaFit scanner at the Donders Center for Cognitive Neuroimaging, using a 32-channel head coil. For anatomical reference, a high-resolution T1-weighted image was collected at the start of each session (3D MPRAGE, TR: 2300 ms, TI: 1100 ms, TE: 3 ms, flip angle: 8 degrees, FOV: 256 x 256 mm, 192 saggital slices, 1-mm isotropic voxels). B0 field inhomogeneity maps (TR: 653 ms, TE: 4.92 ms, flip angle: 60 degrees, FOV: 256 x 256 mm, 68 transversal slices, 2-mm isotropic voxels, interleaved slice acquisition) were acquired. Functional data were acquired using a multi-band accelerated gradient-echo EPI protocol, in 68 transversal slices covering the whole brain (TR: 1500 ms, TE: 38.60 ms, flip angle: 75 degrees, FOV: 210 x 210 mm, 2-mm isotropic voxels, multiband acceleration factor: 4, interleaved slice acquisition).
3t magnetom prismafit scanner
Manufactured by Siemens
Sourced in Germany
The 3T MAGNETOM PrismaFit scanner is a magnetic resonance imaging (MRI) system designed by Siemens. It operates at a field strength of 3 Tesla, providing high-quality imaging capabilities. The scanner is engineered to deliver reliable and consistent performance for diagnostic purposes.
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Lab products found in correlation
5 protocols using 3t magnetom prismafit scanner
1
Multimodal Neuroimaging Protocol for Cognitive Studies
2
Multimodal Neuroimaging Protocol for Cognitive Studies
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MRI data were acquired on a Siemens 3T MAGNETOM PrismaFit scanner at the Donders Center for Cognitive Neuroimaging, using a 32-channel head coil. For anatomical reference, a high-resolution T1-weighted image was collected at the start of each session (3D MPRAGE, TR: 2300 ms, TI: 1100 ms, TE: 3 ms, flip angle: 8 degrees, FOV: 256 x 256 mm, 192 saggital slices, 1-mm isotropic voxels). B0 field inhomogeneity maps (TR: 653 ms, TE: 4.92 ms, flip angle: 60 degrees, FOV: 256 x 256 mm, 68 transversal slices, 2-mm isotropic voxels, interleaved slice acquisition) were acquired. Functional data were acquired using a multi-band accelerated gradient-echo EPI protocol, in 68 transversal slices covering the whole brain (TR: 1500 ms, TE: 38.60 ms, flip angle: 75 degrees, FOV: 210 x 210 mm, 2-mm isotropic voxels, multiband acceleration factor: 4, interleaved slice acquisition).
3
Functional MRI Acquisition and Preprocessing
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Functional MRI data was acquired in 6 runs of 11.9 min on a 3 T Magnetom Prisma Fit Scanner (Siemens Healthcare GmbH, Erlangen, Germany) at the Center for Cognitive Neuroscience Berlin (CCNB), using a 64 channel head coil. Four hundred and seventy‐five functional volumes were acquired per run using a T2*‐weighted gradient‐echo EPI multiband 1 sequence (SMS factor = 3), with interleaved acquisition order and whole brain coverage (TR = 1.5 s; TE = 33 ms; 2.5 × 2.5 × 2.5 mm3 voxel; matrix size = 80 × 80, FOV = 200 mm, flip angle = 70°; 48 slices; gap = 10%). Additionally, a T1‐weighted MPRAGE with 208 sagittal slices, TR = 1930 ms, TE = 3.52 ms, 0.8 × 0.8 × 0.8 mm3 voxel size was acquired.
FMRI data were pre‐processed with SPM12 (Wellcome Trust Centre for Neuroimaging, Institute for Neurology, University College London, UK). Functional data were realigned to the mean image, normalized to MNI space using unified segmentation, interpolated to 2 × 2 × 2 mm3 voxel size, spatially smoothed with an 8 mm FWHM Gaussian kernel, and temporally detrended (Macey et al., 2004 (link)).
FMRI data were pre‐processed with SPM12 (Wellcome Trust Centre for Neuroimaging, Institute for Neurology, University College London, UK). Functional data were realigned to the mean image, normalized to MNI space using unified segmentation, interpolated to 2 × 2 × 2 mm3 voxel size, spatially smoothed with an 8 mm FWHM Gaussian kernel, and temporally detrended (Macey et al., 2004 (link)).
4
Functional MRI Acquisition and Preprocessing
Check if the same lab product or an alternative is used in the 5 most similar protocols
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Functional MRI data was acquired in 6 runs of 11.9 min on a 3 T Magnetom Prisma Fit Scanner (Siemens Healthcare GmbH, Erlangen, Germany) at the Center for Cognitive Neuroscience Berlin (CCNB), using a 64 channel head coil. Four hundred and seventy‐five functional volumes were acquired per run using a T2*‐weighted gradient‐echo EPI multiband 1 sequence (SMS factor = 3), with interleaved acquisition order and whole brain coverage (TR = 1.5 s; TE = 33 ms; 2.5 × 2.5 × 2.5 mm3 voxel; matrix size = 80 × 80, FOV = 200 mm, flip angle = 70°; 48 slices; gap = 10%). Additionally, a T1‐weighted MPRAGE with 208 sagittal slices, TR = 1930 ms, TE = 3.52 ms, 0.8 × 0.8 × 0.8 mm3 voxel size was acquired.
FMRI data were pre‐processed with SPM12 (Wellcome Trust Centre for Neuroimaging, Institute for Neurology, University College London, UK). Functional data were realigned to the mean image, normalized to MNI space using unified segmentation, interpolated to 2 × 2 × 2 mm3 voxel size, spatially smoothed with an 8 mm FWHM Gaussian kernel, and temporally detrended (Macey et al., 2004 (link)).
FMRI data were pre‐processed with SPM12 (Wellcome Trust Centre for Neuroimaging, Institute for Neurology, University College London, UK). Functional data were realigned to the mean image, normalized to MNI space using unified segmentation, interpolated to 2 × 2 × 2 mm3 voxel size, spatially smoothed with an 8 mm FWHM Gaussian kernel, and temporally detrended (Macey et al., 2004 (link)).
5
Brain MRI Characterization of Cerebrovascular Disease
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