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Magnetom avanto mri system

Manufactured by Siemens
Sourced in Germany

The Magnetom Avanto MRI system is a magnetic resonance imaging (MRI) scanner developed by Siemens. It is designed to generate high-resolution images of the body's internal structures using strong magnetic fields and radio waves. The Magnetom Avanto is capable of capturing detailed images of various organs and tissues, which can aid in the diagnosis and monitoring of various medical conditions.

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3 protocols using magnetom avanto mri system

1

Structural and Functional MRI Preprocessing

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Images were acquired on a 1.5 T Siemens Magnetom Avanto MRI system (Siemens, Erlangen, Germany). A high-resolution structural image was created using a T1-weighted sequence (TR = 2.25 s, TE = 2.95 ms, 1 × 1 × 1 mm in-plane resolution). Functional images were acquired using a 2D EPI sequence (TR = 2.02 s, TE = 40 ms, 3 × 3 × 3.5 mm, 26 sagittal slices). Data were pre-processed using SPM8 (Wellcome Trust Centre for Neuroimaging, London, UK). We discarded the first four volumes of every run in order to allow for initial equilibrium. Functional images were first spatially realigned to the mean and then corrected for slice timing. The mean functional image was brought in register with the T1. The T1 was furthermore segmented using SPM8’s segment function, which yielded normalization parameters into MNI space. Finally, functional images were normalized into MNI space, and smoothed (6 × 6 × 6 mm FWHM).
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2

Magnetic Resonance Imaging after MCAO

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MRI was performed on days 1 and 84 post-MCAO on a Siemens 3.0 Tesla Magnetom Avanto MRI system. Utilizing the previously described surgical anesthesia protocol [35 (link)], MRI of the cranium was performed using a 12-channel head coil, 25 cm in diameter, with the pig positioned in supine recumbency. Standard multiplanar magnetic resonance (MR) brain imaging sequences were acquired including T2FLAIR, T2W, DWI, and DTI. T2FLAIR, T2W, DWI, and ADC maps were analyzed using Osirix software (version 5.8.5, Pixme, Geneva, Switzerland). DTI and computed FA values were analyzed using ImageJ software. Analysis of MLS was performed by two trained blinded independent raters on coronal and axial planes on T2-weighted MR images at the level of the septum pellucidum. To determine inter-rater reliability, Pearson’s correlation was conducted on MLS measurements in axial and coronal planes by two raters in both NSC EV–treated and non-treated animals. Pearson’s correlation of raters’ measurements showed a NSC EV axial of R2 = 0.679 (p = 0.0228), NSC EV coronal of R2 = 0.841 (p = 0.0036), non-treated axial of R2 = 0.970 (p < 0.0001), and non-treated coronal of R2 0.936 (p < 0.001) indicating that their measurements were significantly related. Average MLS values of both raters per animal were utilized for all correlation analysis.
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3

Neonatal Brain MRI Imaging Protocol

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MRI (T1- and T2-weighed imaging) scans were obtained within the 4–7 days after birth [34 (link)–36 (link)] when the vital sign of the children was relatively stable. All infants were scanned with a 1.5-T Magnetom Avanto MRI system (Siemens, Erlangen, Germany), including MRI plain0 T1WI and T2WI scans. T1WI sequence parameters: RF pulse repetition time 585 ms, echo time 15 ms. T2WI sequence parameters: RF pulse repetition time 4000 ms, echo time 102 ms, a layer thickness of 4 mm, layer spacing of 0.4 mm, and field of view of 20 × 20 cm. All MRIs in this study were read independently by two radiologists who specialized in neuroimaging, and they discussed their findings together. The basal ganglia/watershed scores were determined as proposed by Barkovich et al. [37 (link)]: 0 = no abnormalities in the basal ganglia or cortex; 1 = an abnormal signal in the basal ganglia or thalamus; 2 = an abnormal signal in the cortex; 3 = an abnormal signal in the cortex and basal nuclei (basal ganglia or thalami); 4 = an abnormal signal in the entire cortex and basal nuclei. All images and qualitative scores were assessed by an experienced radiologist, who was blinded to the serum NSE levels and clinical data.
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