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Ingenia mr scanner

Manufactured by Philips
Sourced in Netherlands

The Ingenia MR scanner is a magnetic resonance imaging (MRI) system developed by Philips. It is designed to capture high-quality images of the human body for diagnostic purposes. The core function of the Ingenia MR scanner is to generate detailed, three-dimensional images of internal structures and organs using powerful magnetic fields and radio waves.

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12 protocols using ingenia mr scanner

1

3T Philips Ingenia MR-Scanner Protocol

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Scanning was performed on a 3T Philips Ingenia MR-Scanner (Philips Healthcare, Best, The Netherlands) on software release R5.1.8 with a custom patch. Standard 32-channel head-receive and 16-channel head/neck-receive coils were used. The following imaging protocol was applied (see Fig. 1):
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2

Healthy Volunteer Brain and Kidney Perfusion Imaging

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The study was approved by the institutional review board and written informed consent was obtained prior to subject participation in the study. The sequence was evaluated on 9 healthy volunteers (age: 25–41 years, 4 females) for brain perfusion imaging and in 5 healthy volunteers (age: 23–39 years, 2 females) for kidney perfusion imaging. All imaging was performed on a 3T Ingenia MR scanner (Philips Healthcare, Best, The Netherlands). Subjects were placed in the supine, head-first position with a 32-channel head coil for brain imaging, while they were positioned supine, feet-first with a 16-channel anterior torso coil and respiratory bellows for kidney imaging.
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3

Neurofeedback for Emotion Regulation

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Neurofeedback was performed at the International Tomography Center at Novosibirsk using a 3 T Philips Ingenia MR scanner. Each session consisted of two parts (the first one 15 min and the second one 10 min). In each odd sessions, both parts were using the neurofeedback condition, while in each even sessions, the second part was a transfer session without feedback signal.
Both, the neurofeedback and the transfer sessions comprised alternating blocks of up- and down-regulation of the hemodynamic activity in the target area, with a duration of 40 and 20 s, respectively. Participants were not provided with predetermined strategies, yet they were told that optimal strategies for upregulation would be related to positive emotions. In order to downregulate the target RoI emotionally, neutral strategies were recommended.
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4

3T Philips Ingenia MR-Scanner Protocol

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Scanning was performed on a 3T Philips Ingenia MR-Scanner (Philips Healthcare, Best, The Netherlands) on software release R5.1.8 with a custom patch. Standard 32-channel head-receive and 16-channel head/neck-receive coils were used. The following imaging protocol was applied (see Fig. 1):
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5

Multimodal MRI with Background Gradient Correction

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The multimodal MRI protocol was performed using a clinical 3T Philips Ingenia
MR-Scanner (Philips Healthcare, Best, The Netherlands) using a 16-channel
head/neck and 32-channel head receive-coil. Custom patches were applied on
software release R5.1.8 to optimize T2* imaging by macroscopic
background gradient correction,32 (link),33 (link) to apply multiband imaging (MB)34 (link) and to improve pCASL by 3D GraSE readout, prolonged labeling and improved
background suppression (BGS).35 Details of the imaging protocol were as follows (Figure 1):
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6

Brain Imaging: T1-weighted MRI and SPECT

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For anatomical reference, a T1-weighted (T1w) MRI scan of the brain was obtained on a 3.0-T Ingenia MR scanner (Philips Healthcare, Best, The Netherlands) using a 32-channel receive-only head coil and the following scan parameters: TR/TE 7/3.18 ms; flip angle 9°; 1 mm isotropic resolution. Individual SPECT scans were co-registered to individual MRI scans using 6-parameter rigid body registration in SPM12 (Wellcome Centre for Neuroimaging, London, UK) (Fig. 2). To optimize registration, a high-intensity striatal mask was superimposed on the T1w scan to resemble the contrast on the SPECT scan.
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7

Multimodal Neuroimaging of GABA and Glutamate

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High-resolution structural imaging and magnetic resonance spectroscopy were acquired using a 3.0 Tesla Philips Ingenia MR scanner (Philips Medical System, Bests, Netherlands). For spectroscopic voxel localization and tissue segmentation, high resolution T1-weighted images were acquired using a three-dimensional T1-weighted magnetization-prepared rapid gradient echo sequence with the following parameters: repetition time (TR) = 7.4 ms, echo time (TE) = 3.4 ms, flip angle (FA) = 8°, field of view (FOV) = 220 × 220 mm2, slice thickness = 1 mm, number of excitation (NEX) = 1,180 contiguous sagittal slices. GABA+ and Glx levels in the VOI were measured using the Mescher-Garwood point-resolved spectroscopy (MEGA-PRESS) sequence with the following parameters: TR = 2,000 ms, TE = 68 ms; number of signal averages = 320, scan duration = 11 min, water suppression method = multiple optimizations insensitive suppression train, second-order pencil beam shimming. During odd-numbered acquisitions, Gaussian inversion pulse was applied at 1.9 ppm3 CH2 resonance of GABA, influencing the J-coupled peak at 3.02 ppm (EDIT-ON). The same pulse was provided symmetrically to the other side of the water peak at 7.5 ppm for even-numbered acquisitions (EDIT-OFF).
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8

Pelvic MRI Segmentation Protocol

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Pelvic MRI was performed by a Philips INGENIA™ MR scanner with a field strength of 3.0 T and the patient in the supine position. The scanning parameters included: Repetition time = 3565 ms; echo time = 80 ms; layer thickness = 5 mm; image matrix = 312 ´ 357, field of view = 250 ´ 340 ´ 166 mm.
The sequence of fast spin-echo (FSE) T2-weighted MRI with a large field of view with fat suppression obtained in the axial plane of the entire pelvis was retrieved from the Picture Archiving and Communication System for image segmentation. A total of 9476 T2-weighted MR images were collected from the enrolled patients. Fifteen patients in the training set were randomly selected by random number tables and 367 images from these patients served for manual labeling. A radiological expert with > 15 years of experience in pelvic MRI labeled three target regions (pelvis, mesorectum, and tumor body) on each of the consecutive T2-weighted images. These regions were represented by drab, yellow, and green, respectively (Supplementary Figure 1), using an open annotation tool named Labelme (available at labelme.csail.mit.edu)[31 ]. Data were transformed into the Common Objects in Context (COCO) dataset format[32 ].
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9

1.5T MRI Acquisition Protocol

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MR imaging was performed using a 1.5T Ingenia MR scanner (Philips Healthcare, Best, The Netherlands). The integrated RF body coil was used for transmission and a torso‐sized RF array coil was used for reception. Transverse T1‐weighted images were acquired using a 3D spoiled gradient‐echo sequence (TR/TE = 7.6/4.6 ms, flip angle = 10, voxel size = 1.33 × 1.33 × 2 mm3, field of view = 320 × 320 × 240 mm3, receiver bandwidth = 271 Hz/pixel) with an acquisition time of 3 min and 39 s. Images were reconstructed using vendor‐supplied routines for image‐based intensity normalization and three‐dimensional gradient nonlinearity correction.
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10

Brain Imaging: T1-weighted MRI and SPECT

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For anatomical reference, a T1-weighted (T1w) MRI scan of the brain was obtained on a 3.0-T Ingenia MR scanner (Philips Healthcare, Best, The Netherlands) using a 32-channel receive-only head coil and the following scan parameters: TR/TE 7/3.18 ms; flip angle 9°; 1 mm isotropic resolution. Individual SPECT scans were co-registered to individual MRI scans using 6-parameter rigid body registration in SPM12 (Wellcome Centre for Neuroimaging, London, UK) (Fig. 2). To optimize registration, a high-intensity striatal mask was superimposed on the T1w scan to resemble the contrast on the SPECT scan.
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