The largest database of trusted experimental protocols

Signa hdx platform

Manufactured by GE Healthcare
Sourced in United States

The Signa HDx platform is a MRI system developed by GE Healthcare. It is designed to provide high-quality imaging capabilities for various clinical applications. The core function of the Signa HDx platform is to generate detailed, high-resolution images of the internal structures of the human body using magnetic resonance imaging (MRI) technology.

Automatically generated - may contain errors

8 protocols using signa hdx platform

1

Cerebral Vascular Reactivity MRI Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
All MRI scans were performed on a 3.0T scanner (Signa HDX platform, GE Healthcare, Milwaukee, Wisconsin, USA) with an 8-channel phased array head coil. BOLD MR CVR parameters: T2*-weighted echoplanar gradient-echo sequence (TR 2,000 ms, TE 30 ms, flip 85°, voxel size range 3.75×3.75×5 mm to 3 mm isotropic, no gap, field of view 24×24 cm, matrix 64×64, 255 temporal frames). A high resolution T1-weighted image as anatomical correlate was done using the following parameter: 1.0 mm thick, matrix 256×256, field of view 22×22 cm.
+ Open protocol
+ Expand
2

Cerebral Blood Flow Regulation via fMRI

Check if the same lab product or an alternative is used in the 5 most similar protocols
For all scans, MRI was performed on a 3.0T scanner (Signa HDX platform, GE Healthcare, Milwaukee, Wisconsin, USA) with an 8-channel phased array head coil. T1-weighted anatomical images of the entire brain were acquired using a three-dimensional spoiled gradient echo pulse sequence (1.0 mm thick, matrix 256×256, field of view 22×22 cm). BOLD MR CVR data was acquired for the entire brain using a T2*-weighted echoplanar gradient-echo sequence (TR 2000 ms, TE 30 ms, flip 85°, slice thickness 5.0 mm, no gap, field of view 24×24 cm, matrix 64×64, 255 temporal frames) during manipulation of arterial CO2.
+ Open protocol
+ Expand
3

3T MRI Brain Imaging Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
Subjects underwent MRI scans on either a 3-Tesla GE system (Signa HDx platform, GE Healthcare, Milwaukee, Wis) or a 3-Tesla Philips Achieva system (Philips Medical Systems, Best, Netherlands) using an eight-channel phased array head coil. Subjects were asked to refrain from heavy exercise and drinking alcohol or caffeine on the day of each scan. The image acquisition parameters were as follows, with values provided for SHSC/TWH: T1-weighted 3D spoiled gradient echo sequence [slice thickness = 1.2 mm (SHSC)/1.5 mm (TWH); no interslice gap; matrix size = 256 × 256; field of view = 22 × 22 cm; nominal voxel size  = 0.85 × 0.85 × 1.2/0.85 × 0.85 × 1.5 mm; flip angle = 8 / 20°; TE = 2.3/3 ms; TR = 7.8/9.5 ms] and BOLD fMRI using a T2*-weighted echoplanar imaging gradient echo sequence [slice thickness = 3.0/5.0 mm; field of view = 24 × 24 cm; matrix size = 64 × 64; nominal voxel size = 3.75 × 3.75 × 3/3.75 × 3.75 × 5 mm; flip angle = 85/90°; TE = 30 ms; TR = 2000 ms].
+ Open protocol
+ Expand
4

High-Resolution Structural and Functional Brain Imaging

Check if the same lab product or an alternative is used in the 5 most similar protocols
All subjects were scanned on a 3-Tesla GE system MRI scanner (Signa HDx platform, GE Healthcare, Milwaukee, WI, USA), using an eight-channel phased array head coil at Toronto Western Hospital.
Each subject had a whole-brain high-resolutionT1-weighted 3D spoiled gradient echo (FAST-SPGR) sequence acquired first with the following parameters: TI = 450 ms, TR = 7.88 ms, TE = 3 ms, flip angle = 12°, voxel size = 0.859 × 0.859 × 1 mm, matrix size = 256 × 256, 146 slices, field of view = 24 × 24 cm, no interslice gap.
After the anatomical scan, a BOLD fMRI T2*-weighted echoplanar imaging gradient echo (EPI-GRE) sequence was acquired with the following parameters: TR = 2400 ms, TE = 30 ms, flip angle = 70°, 41 slices, voxel size = 3.5 mm3, matrix size = 64 × 64, number of frames = 335, field of view = 24 × 24 cm.
+ Open protocol
+ Expand
5

BOLD Cerebrovascular Reactivity Imaging

Check if the same lab product or an alternative is used in the 5 most similar protocols
All studies were performed at the Toronto Western Hospital on a 3-Tesla GE MRI system (Signa HDx platform, GE Healthcare, Milwaukee, WI, USA) using an eight-channel phased array head coil. A third generation RespirAct TM gas blender was employed for control of P ET CO 2 during the BOLD CVR sequence. All patients underwent T1-weighted structural imaging, followed by a T2*-weighted axial single-shot BOLD CVR image, 2D FLAIR image, and a proton density/T2-weighted sequence. Full imaging parameters are included in Supplement 1.
+ Open protocol
+ Expand
6

Multimodal Brain Imaging with Respiratory Manipulation

Check if the same lab product or an alternative is used in the 5 most similar protocols
The scans were acquired on a 3-Tesla scanner (HDx Signa platform, GE healthcare, Milwaukee, WI, USA) with an 8-channel head coil. The same fast spoiled gradient echo (FSPGR) T1-weigthed scan and two BOLD sequences with identical scanning parameters that were each 13 minutes and 20 seconds long, were acquired for all participants. The FSPGR scan was a high-resolution T1-weighted scan with a 3D spoiled gradient echo sequence. The following parameters were used: TI = 450 ms, TR 7.88 ms, TE = 3 ms, flip angle = 12°, voxel size = 0.859 × 0.859 × 1 mm, matrix size = 256 × 256, 146 slices, field of view =24 × 24 cm, no interslice gap. Next, the two BOLD sequences consisted of a T2*-weighted echoplanar imaging gradient during the PetCO2 and PetO2 manipulation. The following sequence parameters were used: TR = 2400 ms, TE = 30 ms, flip angle = 85°, 41 slices, voxel size = 3.5 mm3 and matrix size = 64 × 64.
+ Open protocol
+ Expand
7

Cerebrovascular Reactivity Imaging in Sickle Cell Disease

Check if the same lab product or an alternative is used in the 5 most similar protocols
The images acquired from both the HC and SCD patient groups were identical. The CVR scan was acquired on a 3‐Tesla GE scanner (HDx Signa platform, GE healthcare) with an 8‐channel head coil at Toronto Western Hospital. All participants completed an anatomical scan followed by a BOLD sequence scan. In addition, the SCD patient group was subject to further clinical scans as requested by their physicians including axial T2 flair, 3D ASL, DWI and EPI GRE. First, a whole‐brain coverage high‐resolution T1‐weighted 3D spoiled gradient echo sequence (anatomical images) was acquired with the following parameters: TI = 450 ms, TR = 7.88 ms, TE = 3 ms, flip angle = 12°, voxel size = 0.859 × 0.859 × 1 mm, matrix size = 256 × 256, 146 slices, field of view = 24 × 24 cm and no interslice gap. Second, a BOLD fMRI T2*‐weighted echoplanar imaging gradient echo sequence was attained with the following parameters: TR = 2400 ms, TE = 30 ms, flip angle = 85°, 41 slices, voxel size = 3.5x3.5 mm, matrix size = 64 × 64, number of frames = 335, field of view = 24 × 24 cm.
+ Open protocol
+ Expand
8

3T fMRI Acquisition Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
A 3-Tesla scanner (HDx Signa platform, GE healthcare, Milwaukee, WI, USA) with an 8-channel head coil was used in these experiments. The protocol consisted of a high-resolution T1-weighted scan followed by one BOLD sequence scan. The high-resolution T1-weighted scan was acquired using a 3D spoiled gradient echo sequence with the following parameters: TI = 450 ms, TR 7.88 ms, TE = 3 ms, flip angle = 12°, voxel size = 0.859 × 0.859 × 1 mm, matrix size = 256 × 256, 146 slices, field of view = 24 × 24 cm, no interslice gap. The BOLD scan was acquired during normocapnic PetO2 manipulation using a T2*-weighted gradient echoplanar imaging sequence with the following parameters: TR = 1,500 ms, TE = 30 ms, flip angle = 73°, 29 slices voxel size = 3 mm isotropic voxels and matrix size = 64 × 64.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!