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32 channel receive head coil

Manufactured by Philips
Sourced in Netherlands

The 32-channel receive head coil is a medical imaging device designed to be used with Magnetic Resonance Imaging (MRI) systems. Its primary function is to receive and amplify the radio frequency (RF) signals generated by the target area during an MRI scan, which are then processed to produce high-quality images of the patient's head and brain.

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19 protocols using 32 channel receive head coil

1

Resting-state fMRI Acquisition Protocol Using 3T MRI Scanner

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MRI scans were acquired using the Philips Medical Systems (Best, Netherlands) Ingenia wide-bore dStream 3T MRI scanner, with a 32-channel receive head coil. Single shot gradient-echo echoplanar imaging (EPI) was used for acquiring fMRI data. The fMRI acquisition parameters were: SENSE in-plane acceleration factor 1.5, multiband factor 3, repetition time 1625 ms, echo time 30 ms, flip angle 52°, field of view 240 mm (anterior-to-posterior) × 240 mm (left-to-right) × 125.70 mm (foot-to-head), in-plane resolution 2.5 mm × 2.5 mm, 45 axial slices, slice thickness 2.5 mm, interslice gap 0.30 mm, 420 repetitions per run after 12 dummy acquisitions, and total duration 11 minutes 22 seconds. Subjects completed the resting state fMRI scan with eyes open while looking at a black fixation cross on a white screen. Greater detail regarding MRI acquisition parameters is available in Supplementary File.
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2

Multi-Modal Neuroimaging of Healthy Subjects

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MRI data were acquired using a 3-Tesla Achieva scanner (Philips Healthcare, Netherlands) equipped with 80 mT/m gradients and a 32–channel receive head coil. Diffusion weighted images were acquired using a single-shot spin-echo echo-planar imaging sequence (repetition time [TR] = 11.8 s, echo time [TE] = 50.1 ms, field of view [FOV] = 220 × 220 mm2, N transversal slices = 60, slice thickness = 2 mm, acquisition matrix = 112 × 110). Diffusion was recorded along 64 directions with a b-value of 1000 s/mm2. Additionally, one non–diffusion–weighted b = 0 s/mm2 scan was performed. To aid with anatomical registration of diffusion weighted images, T1–weighted structural images were acquired with 1 mm isotropic resolution (TR = 8.1 ms, TE = 3.7 ms).
Preprocessing was performed using QSIPrep version 0.12.2 (Cieslak et al., 2021 (link)), which is based on Nipype (Gorgolewski et al., 2011 ). T1–weighted images were corrected for intensity non-uniformity and skull-stripped using ANTs tools (Avants et al., 2011 (link)), then used as a structural reference for registration of diffusion images. To correct diffusion images for head motion and eddy current-induced image distortions, FSL eddy was applied (Andersson and Sotiropoulos, 2016 (link)). FA maps were computed using tools from TractSeg (Wasserthal et al., 2018 (link)).
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3

Diffusion MRI data acquisition protocol

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MRI data acquisition was performed on a 3T whole-body MR scanner (Achieva, Philips Healthcare, Best, the Netherlands), equipped with 80 mT/m gradients and a 32-channel receive head coil. Diffusion data were acquired using a diffusion-weighted single-shot spin-echo echo-planar imaging sequence (ssh SE-EPI sequence) with the following parameters: repetition time (TR) = 6.64 s, echo time (TE) = 53.6 ms, field of view (FOV) = 240 × 240 mm2, 50 contiguous transversal slices, slice thickness = 2.5 mm, acquisition matrix = 96 × 96, SENSE factor = 2.5, partial Fourier encoding = 60%. The slices were positioned parallel to the anterior and posterior commissure defined on a T1-weighted midline sagittal survey image. Diffusion acquisition was performed along 32 directions with a b-value of 1000 s/mm2 and two signal averages (NSA = 2). Additionally, 4 non-diffusion-weighted b = 0 s/mm2 scans were acquired resulting in a scan time of 8 min 31 s. For structural reference and anatomical priors for the tracking algorithm, T1-weighted images were recorded using a three-dimensional magnetization prepared rapid gradient-echo (MP-RAGE) sequence with 1 mm isotropic resolution.
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4

Multimodal Brain Imaging of Precision Grip

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Magnetic resonance imaging (MRI) was performed with a Philips Achieva 3.0 T scanner and a 32-channel receive head coil (Philips, Best, The Netherlands). During the precision grip task, whole-brain fMRI scans were acquired with an Echo Planar Imaging (EPI) sequence with repetition time (TR) = 2500 ms, echo time (TE) = 30 ms, and flip-angle of 80˚. Each brain volume consisted of 42 axial slices acquired in interleaved order with a slice thickness of 3 mm, resulting in a 3x3x3 mm voxel resolution and a field-of-view (FOV) of 192x192x126 mm. For quantifying lesion load and overall brain atrophy, structural MRI including T1- and T2-weighted and Fluid Attenuated Inversion Recovery (FLAIR) images were obtained. The T1-weighted image was acquired with a sagittal magnetization prepared rapid acquisition gradient echo (MPRAGE) sequence (TR = 6 ms, TE = 2.70 ms, flip-angle = 8°, 0.85 mm isotropic voxel size and a FOV of 245x245x208 mm). The T2-weighted image was acquired with a turbo spin echo sequence (TR = 2500 ms, TE = 270 ms, flip-angle = 90°, 0.85 mm isotropic voxel size and a FOV of 245x245x190 mm). The FLAIR image was acquired with a TR = 4800 ms, TE = 327 ms and an isotropic voxel size of 1 mm3 resulting in a FOV of 256 × 256 × 202 mm.
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5

Neuroimaging Protocol for Real-time Neurofeedback

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The MRI images were acquired on a 3 Tesla MRI scanner (Philips Achieva, upgraded to dStream platform), equipped with a 32-channel receive head coil. Functional images for rt-fMRI neurofeedback were acquired with a T2∗-weighted gradient-echo-planar sequence with a repetition time (TR) = 2000 ms, echo time (TE) = 35 ms, flip angle = 82°, FOV = 220 mm × 220 mm, voxel size = 2 × 2 × 4 mm3, matrix size = 112 x 112, and 27 slices per volume with whole-brain coverage. 170 functional images were collected during each neurofeedback run (duration = 5.8 min). Anatomical images were collected with a 3D MPRAGE sequence: TR = 9.32 ms, TEs = 4.59 ms, flip angle = 8°, FOV = 240 mm × 240 mm, voxel size = 1 × 1 × 1 mm3, 160 slices, and duration = 3.7 min.
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6

Resting-State fMRI Protocol for 3T MRI

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MRI scans were acquired using a Philips Medical Systems (Best, Netherlands) Ingenia wide-bore dStream 3 T MRI scanner, with a 32-channel receive head coil. A spin-echo echo planar pulse sequence was used with: parallel imaging acceleration-factor 2.0, repetition-time 2500 ms, echo-time 75 ms, flip-angle 90 degrees, field-of-view 240 mm (anterior to posterior) × 240 mm (left to right) × 123.75 mm (foot to head), in-plane resolution 3.75 mm × 3.75 mm, 25 axial slices, slice-thickness 3.75 mm, interslice-gap 1.25 mm, 112 repetitions per run after 10 dummy acquisitions. Total duration per run was approximately 5 min.
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7

3T MRI Protocol for T1-Weighted Imaging

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At both time points, MRI data for all subjects were collected on the same 3 T Philips Achieva whole-body scanner equipped with a 32-channel receive head coil, using the same standard T1-weighted 3D magnetization-prepared rapid gradient echo (MPRAGE) pulse sequence. Image parameter were: repetition time (TR) = 8.08 ms, echo time (TE) = 3.7 ms, field of view (FOV) = 240 × 240 mm2, 160 slices, voxel size of 1 × 1 × 1 mm3.
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8

Structural Brain MRI of Meal Response

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Structural brain MRI images were collected as part of a wider MRI protocol including functional MRI brain responses to a test meal. Participants were scanned on a 3T Philips Achieva scanner (Philips Medical Systems, Best, Netherlands) with a 32-channel receive head coil. Brain scans were acquired with a T1-weighted MPRAGE sequence orientated along the AC-PC line (1mm3,TE/TR = 8.3/3.8ms,flip angle = 8°,SENSE = 2,160 slices,256 × 256 matrix).
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9

Multimodal Brain Imaging with pCASL

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Imaging was performed on a Philips Achieva 3.0 T whole-body scanner (Best, The Netherlands) and a 32-channel receive head coil. Anatomical images were acquired 60 min after drug administration followed by a resting-state BOLD scan (data reported:16 (link)) and the resting state pseudo-continuous ASL (pCASL) scan (80–100 min after drug administration).
High-resolution T1-weighted anatomical images were collected using a voxel size of 1 × 1 × 1 mm3 (n = 60) or 0.7 × 0.7 × 0.7 mm3 (n = 10). ASL data were acquired using a pCASL sequence with the following parameters: TR = 4400 ms; TE = 20 ms; FOV = 240 × 240 mm2; matrix size = 80, 23 slices with a voxel size = 3 × 3 ×  7 mm, and no gap; gradient echo single shot EPI; SENSE 2.5; post-labeling delay of 1525 ms; label duration: 1650 ms; number of dynamics: 60 (n = 39) or 50 (n = 31). One dynamic consisted of a control and a labeled image, resulting in a total scan time of 4 min 24 s (n = 39) or 3 min 40 s (n = 31).
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10

Functional MRI Acquisition Protocol

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Functional magnetic resonance imaging (fMRI) data were acquired on a Philips 3.0 T Achieva system with a 32 channel receive head coil (Philips Medical Systems, Best, Netherlands). The raw fMRI data acquired from each subject were converted to ANALYZE image format using SPM conversion software (http://sourceforge.net/projects/r2agui/files/r2agui/). 3D-SPGR (resolution=1 mm × 1 mm × 1 mm) and Fluid Attenuation Inversion Recovery (FLAIR) scans were also acquired for each subject. The fMRI pulse sequence used in this study was a gradient echo EPI that is sensitive to the BOLD effect (Ogawa et al. 1990 (link)). Images were acquired in the transverse plane using a single shot sequence with SENSE factor = 2.0, with a repetition time = 2000 ms, echo time = 25 ms, flip angle = 80°, number of axial slices = 43, field of view = 220 mm × 220 mm, in-plane resolution = 3.00 mm × 3.00 mm, slice thickness = 3.5 mm without gap, 200 repetitions following six dummy scans, matrix = 64 mm × 64 mm, run duration = 6 min 53 s. The start of each behavioral protocol was automatically triggered by the MRI scanner to coincide with the RF pulse at the start of the first acquired image. Each subject underwent 5 runs, each separated by 1–2 minutes of rest that includes a re-reading of the scripted instructions.
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