Purpose: To optimize timing parameters in an intermolecular double-quantum coherence (iDQC) imaging pulse sequence for overall image signal-to-noise ratio (SNR) and blood oxygenation level-dependent (BOLD) sensitivity for brain functional imaging.
Material And Methods: Fresh human blood was measured under different oxygenation conditions, and human brain functional magnetic resonance (fMR) images in three normal volunteers were obtained, using iDQC techniques at 1.5 T. The dependence of SNR and BOLD sensitivity was measured as a function of time delays after the iDQC evolution period.
Results: A time delay after the iDQC evolution period tau can be adjusted either to refocus the dephasing accumulated during tau, thus increasing SNR, with full rephasing occurring at delay = +/-2tau (for iDQC order n = +/-2), or to enhance BOLD effects with consequent reduced image SNR at delay = 0.
Conclusion: Image SNR and BOLD sensitivity often impose different requirements for iDQC image sequence design and timing parameter selections. It is therefore important to select properly relevant parameters for different applications.
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http://dx.doi.org/10.1002/jmri.10208 | DOI Listing |
Fluids Barriers CNS
December 2024
C.J. Gorter MRI Center, Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.
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Cognitive Neuroscience Division, Department of Neurology, Columbia University Irving Medical Center, New York, NY.
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Veterinary Diagnostic Laboratory, College of Veterinary Medicine, Kansas State University, Manhattan, KS, USA; Department of Diagnostic Medicine/Pathobiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS, USA. Electronic address:
The emergence of SARS-CoV-2 raised concerns about the potential for interspecies transmission, particularly among domestic animals. We evaluated the seroprevalence of SARS-CoV-2 antibodies in domestic cats from various sites in North America. A total of 216 serum samples collected between December 2019 and February 2022, were analyzed using four different enzyme-linked immunosorbent assays (ELISAs), including a commercial surrogate virus neutralization test (sVNT), a commercial double antigen test (dN ELISA), and two in-house developed indirect ELISAS based on receptor-binding domain (RBD iELISA) and the nucleocapsid (N iELISA) proteins, respectively.
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Program in Advanced Imaging Research and Department of Radiology, Children's Hospital of Philadelphia, Philadelphia, PA, USA (JI Berman, L Bloy, S Ward, TPL Roberts) Department of Radiology, University of Pennsylvania, Philadelphia, PA, USA (JI Berman, TPL Roberts).
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