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3 t prisma magnetom vd13

Manufactured by Siemens

The 3 T Prisma Magnetom VD13 is a magnetic resonance imaging (MRI) system manufactured by Siemens. It operates at a magnetic field strength of 3 Tesla, providing high-quality images for clinical and research applications.

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2 protocols using 3 t prisma magnetom vd13

1

Multimodal Brain Imaging of Social and Reward Processing

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All scans were performed using a Siemens 3 T Prisma Magnetom VD13 echo speed scanner with a 20-channel head coil located at the Wohl Institute for Advanced Imaging at the Tel-Aviv Sourasky Medical Center. Structural scans included a T1-weighted 3D axial spoiled gradient echo (SPGR) pulse sequence (repetition time/echo time [TR/TE] = 1860/2.74 ms, flip angle = 8°, voxel size = 1 × 1 × 1 mm, field of view = 256 × 256 mm, slice thickness = 1 mm).
Functional whole-brain scans of all fMRI tasks were performed in an interleaved bottom-to-top order with a T2*-weighted gradient echo planar imaging pulse sequence (TR/TE = 2500/30 ms, flip angle = 82°, voxel size = 2.3 × 2.3 × 3 mm, the field of view = 220 × 220 mm, slice thickness = 3 mm, 42 slices per volume). For three participants in the social feedback task and the guided self-evaluation task, the TE was 35, flip angle was 90° and 38 slices per volume were obtained. These participants were included in the analysis. The number of volumes acquired for each of the fMRI tasks was as follows: social feedback—246; guided self-evaluation—2 sessions including 118 volumes each; reward—2 sessions including 117 volumes each.
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2

Structural and Functional Brain Imaging

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All scans were performed using a Siemens 3T Prisma Magnetom VD13 echo speed scanner with a 20‐channel head coil located at the Wohl Institute for Advanced Imaging at the Tel‐Aviv Sourasky Medical Center. Structural scans included a T1‐weighted 3D axial spoiled gradient echo (SPGR) pulse sequence (time repetition [TR]/TE = 7.92/2.98 ms, flip angle = 15°, pixel size = 1 mm, FOV = 256 × 256 mm, slice thickness = 1 mm). Functional whole‐brain scans were performed in interleaved order with a T2*‐weighted gradient echo planar imaging pulse sequence (TR/TE = 2500/35 ms, flip angle = 90°, pixel size = 1.56 mm, FOV = 200 × 200 mm, slice thickness = 3.1 mm, 38 slices per volume). Anatomical SPGR data were standardized to 1 × 1 × 1 mm and transformed into Talairach space. The preprocessing of the functional data was performed using BrainVoyager QX version 2.1.4. Head motions were detected and corrected using trilinear and sinc interpolations, respectively, applying rigid body transformations with three translation and three rotation parameters. SPGR images were then manually coregistered with the corresponding functional maps. Several datasets were excluded due to exaggerated head movements (>2.5 mm) from the analysis of each run. Data of six participants were excluded from run‐1, of five participants from run‐2, of five participants from run‐3 and of five participants from run‐4.
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