Additionally, a T1 BRAVO ‘ex vivo’ acquisition (TR = , TE = , TI = 450 , FA = 12°) of the brain placed inside the 3D-printed slicer (see below) was performed on a 3T Signa PET/MR scanner (GE Healthcare, Chicago, IL, USA) right before slicing. It should, however, be noted that brain fixation has caused convergence of the T1 values of white and gray matter, as reported in [17 (link),18 (link)]. Consequently, the acquired ex vivo T1 image rather has a proton-density (PD) contrast. Furthermore, note that drainage of the extracellular fluid made it impossible to delineate edema regions on postmortem T2-FLAIR images, motivating the use of a registered antemortem T2-FLAIR image for edema delineation hereafter.
3t signa pet mr scanner
The 3T Signa PET/MR scanner is a hybrid medical imaging device that combines positron emission tomography (PET) and magnetic resonance imaging (MRI) technologies. It enables simultaneous acquisition of both PET and MRI data, providing comprehensive information about the structure and function of the examined body part.
4 protocols using 3t signa pet mr scanner
Multimodal MRI Registration for Brain Edema Delineation
Additionally, a T1 BRAVO ‘ex vivo’ acquisition (TR = , TE = , TI = 450 , FA = 12°) of the brain placed inside the 3D-printed slicer (see below) was performed on a 3T Signa PET/MR scanner (GE Healthcare, Chicago, IL, USA) right before slicing. It should, however, be noted that brain fixation has caused convergence of the T1 values of white and gray matter, as reported in [17 (link),18 (link)]. Consequently, the acquired ex vivo T1 image rather has a proton-density (PD) contrast. Furthermore, note that drainage of the extracellular fluid made it impossible to delineate edema regions on postmortem T2-FLAIR images, motivating the use of a registered antemortem T2-FLAIR image for edema delineation hereafter.
Multimodal Imaging of Sinonasal Pathologies
Dopamine D2/3 Receptor and Fear Conditioning
Participants were positioned supine in the combined Signa 3T PET/MR scanner (GE Healthcare) with their heads lightly fixated inside the head coil. A bolus (20 s) of the selective dopamine D2/3 receptor antagonist [11C]raclopride was injected through a venous catheter and followed by constant infusion during the 90 min of PET data acquisition. Following 50 min of resting PET data collection, participants underwent a differential fear conditioning paradigm during collection of blood-oxygenation-level dependent (BOLD) fMRI and skin conductance. The PET scanning continued 20 min after the fear conditioning paradigm.
Deuterated Glucose Imaging in CNS Lesions
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