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Signa explorer

Manufactured by GE Healthcare
Sourced in United States

The Signa Explorer is a magnetic resonance imaging (MRI) system developed by GE Healthcare. It is designed to provide high-quality imaging capabilities for healthcare professionals. The core function of the Signa Explorer is to generate detailed images of the body's internal structures using strong magnetic fields and radio waves.

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33 protocols using signa explorer

1

Comprehensive MRI Acquisition and Analysis Protocol for Tumor Characterization

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All the MRI images were acquired using a 1.5 T MRI scanner (SIGNA Explorer, GE Healthcare, Waukesha, WI, USA) with a 16-channel body array coil. To reduce peristaltic artifacts, all the subjects fasted for 6 h and were given intravenous hyoscine butylbromide (Buscopan, Boehringer Ingelheim, Ingelheim am Rhein, Germany) before MRI examinations. Standardized MRI protocol, including conventional T2W, T1W, dynamic contrast-enhanced MRI (DCE-MRI), DWI (b = 0, 400, 800) and synthetic MRI, are summarized in Table 1.
The image post-processing was performed on a 64-bit Advantage Workstation (GE Healthcare, Waukesha, WI, USA), which generated the parametric maps (T1, T2, PD and ADC), as well as synthetic contrast-weighted images automatically. The mean of the T1/T2/PD/ADC maps were calculated inside the region-of-interest (ROIs) for all slices that contained the tumor.
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2

Rapid brain imaging with silent MRI

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A newly developed silent mode MRI and a sequence allowed us to capture the participants’ brain structure in less than 30 s (19 (link)). Consequently, with the help of an MRI-compatible video presentation system and an MRI-compatible headphone system, we were able to conduct MRI without sedation for the other 21 children. The following methods for MR image acquisition have been described before (11 (link)). A 1.5-T MRI scanner (SIGNA Explorer; GE Healthcare, United States) was used to collect structural brain images from all participants. The three-dimensional high-resolution T1-weighted gradient-echo and Silenz pulse sequence images were used as an anatomical reference. The imaging parameters were as follows: TR = 435.68 ms, TE = 0.024 ms, flip angle = 7°, FOV = 220 mm, matrix size = 256 × 256 pixels, slice thickness = 1.7 mm, total of 130 transaxial images.
For these 21 participants, we co-registered the MEG and their own MR images following the marker locations. The markers for MEG and MRI were the frontal midline, parietal, and bilateral mastoid processes. For the MEG, we used four coils to generate a magnetic field. For MRI, we used four pieces of lipid capsule as markers. Furthermore, we identified points on the mastoid processes, nasion, and skull surface visually on MRI. Approximately 15–25 points were depicted for each participant.
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3

Temporal Lobe Hypoplasia Prevalence

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The decision number and approval date for this IRBapproved study are 2021-11/7 and 11/11/2021, respectively. MRI images of 5163 patients who applied to the training and research hospital for various reasons between 1 September 2020, and 31 August 2021, who underwent brain MRI, were reviewed retrospectively. TH distribution rates were determined according to the gender of the patients, the side of the hypoplasia, and the reasons for applying to the clinic.
Exclusion criteria included intracranial mass lesion, intracranial haemorrhage, intracranial operation, intracranial stab wound and radiotherapy history, diagnosed congenital syndrome-malformation, and hydrocephalus.
Patients were examined in 1.5 Tesla (Signa Explorer, GE, Healthcare, USA) and 3 Tesla (Magnetom Skyra, Siemens, Healthcare, Germany) MR systems. The protocol included at least axial T1- and T2-weighted images (WI), sagittal T2-WI, and axial fluid-attenuated inversion recovery (FLAIR) images.
A radiology research assistant (H.İ.Ş; 3 years of experience) analysed all MRI scans. MRI images of patients with TH were re-evaluated and confirmed by an experienced radiologist (Ö.Ü; 20 years of neuroradiology experience).
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4

Standardized MRI Evaluation of Shoulder Angles

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Shoulder examinations were evaluated with a 1.5-T MRI device (SIGNA Explorer;
General Electric). Angle measurements were made on coronal T1-weighted sequence
images at the radiology workstation (Sectra Workstation IDS7). The parameters
for the T1-weighted sequence images were as follows: repetition time/echo time =
608/10.4 ms, field of view = 170 mm, section thickness = 4 mm, cross section = 4
mm, number of excitations = 4, matrix = 256 × 160. All scans were taken with the
patients in the supine position, with the arm fixed in abduction and the palm of
the hand in the medial neutral position. In this way, we ensured the
standardization of the shots. All measurements were made on the workstation by
magnifying the image 4 times.
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5

Cardiac MRI Assessment of Myocarditis

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CMR examinations were performed on a 1.5 Tesla system (Signa Explorer, General Electric, Milwaukee, USA). A 16-channel body coil was used for data acquisitions. Cine balanced steady-state free precession (b-SSFP) images were obtained from cardiac base-to-apex as short-axis stack images with retrospective electrocardiogram triggering and breath holding. The image analysis was made on a remote workstation (Advantage Windows, version 4.3, and version 4.4; GE Medical Systems) with cardiac analysis software (ReportCard 2.0; GE Medical Systems). In each patient, end-diastolic volume (EDV), end-systolic volume (ESV), stroke volume and LVEF were calculated, divided by body surface area to obtain indexed right ventricle volumes. LGE imaging was performed approximately 10 min after administration of body weight-appropriate gadobutrol. To evaluate the LGE, all short-axis slices from basis to apex were assessed for zones of normal myocardium. Scar distribution types were then assessed in accordance with the transmural, focal and diffuse involvement. All images were analysed by one cardiologist. The study was accepted as positive for myocarditis, considering the Lake Louise criteria.
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6

Standardized Hip MRI Protocol

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MRI examinations were performed using 1.5-T (Signa Explorer, GE Healthcare, USA) or 3.0-T (Discovery MR 750w, GE Healthcare, U.S.A.) MR scanners with the unenhanced hip protocol. The standard protocol of 1.5-T MRI consisted of axial T1-weighted (repetition time (TR)/echo time (TE) 632/9 ms, 4-mm slice thickness, 0.5-mm gap), axial and coronal T2-weighted (TR/TE 3102/77 ms, 4-mm slice thickness, 0.5-mm gap), and T2-weighted fat saturation (TR/TE 4500/77 ms, 4-mm slice thickness, 0.5-mm gap) sequences through the entire pelvis using a 32-channel body coil. The field of view (FOV) for each sequence was 42 × 42 cm with a 384 × 256 matrix. The protocol of 3.0-T MRI consisted of axial T1-weighted (TR/TE 455/8 ms, 4-mm slice thickness, 0.5-mm gap), axial and coronal T2-weighted with fat saturation (TR/TE 4287/81 ms, 4-mm slice thickness, 0.5-mm gap), and coronal short tau inversion recovery (STIR) sequence (TR/TE 8291/47 ms, inversion time 150 ms, 4-mm slice thickness, 0.5-mm gap) using a 23-channel body coil with a FOV of 41 × 41 cm and 416 × 288 acquisition matrix.
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7

Diffusion-Weighted Imaging Analysis Protocol

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Diffusion-weighted imaging’s (DWI) were obtained using two 1.5 T-magnetic resonance imaging (MRI) units (GE Signa HDxt and Signa Explorer; GE, Milwaukee, WI, USA). DWIs were acquired in the axial plane with parameters field of view: 25 mm, repetition time: 5000 ms, echo time: 100 ms, acquisition time: 1, number of excitations: 1, and b values of 0 and 1000 s/mm2, isotropically weighted. DWI yielded 20 contiguous slices that were 7 mm thick and axial-oblique. Apparent diffusion coefficient (ADC) map was automatically generated from DWI at b = 0 and b = 1000 s/mm2. The ADC maps were checked to make sure “real” diffusion disturbance. A visual evaluation was performed.
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8

Retrospective Brain MRI Dataset Analysis

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Brain MRI datasets obtained within the 5 years prior to the study were analyzed retrospectively. If the patient had more than one neuroimaging scan, the images were compared to assess the appearance of new lesions. MRI was requested for patients who had not undergone neuroimaging during the past 5 years. Brain MRI was performed with a 1.5-T magnetic resonance unit (Signa Explorer, GE Medical Systems, Milwaukee, WI). T1-weighted [echo time (TE)/repetition time (TR), 11 ms/550 ms], T2-weighted (TE/TR, 93 ms/4000 ms), fluid-attenuated inversion recovery (TE/TR/inversion time, 110 ms/10000 ms/2250 ms), and diffusion-weighted (TE/TR, 105 ms/5200 ms) imaging was performed.
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9

Structural Brain Imaging Using 1.5T MRI

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A 1.5 T MRI scanner (SIGNA Explorer; GE Healthcare, USA) was used to obtain structural brain images from all participants and to compute individual head models for source analysis. The T1-weighted gradient echo and Silenz pulse sequence (TR = 435.68 ms, TE = 0.024 ms, flip angle = 7°, FOV = 220 mm, matrix size = 256 ×256 pixels, slice thickness = 1.7 mm, a total of 130 transaxial images) images were used for anatomical reference. All participant's MRI images were recorded.
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10

MRI Contrast Evaluation of U87 Cells

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For MRI, 8,000 U87 cells were seeded and incubated for two days in a 6 well-plate (Sarstedt, Nümbrecht, Germany). After that, a PEGNIO/QDs/MIONs/Tf dispersion sample was applied to the cells for 2 h. Then, the medium was removed from the wells and the cells were washed with PBS twice. Next, pure medium was added into the wells, and MR imaging was carried out using the T2-weighted state of the SIGNA Explorer (1.5 T, 60 cm) by GE Healthcare (Chicago, IL, USA). Then, the amount of contrast was measured with the Image J software by generating an MRI histogram. The negative control was prepared with U87 cells using only the medium under the same conditions.
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