scholarly journals Proton MRI of the Lung: How to Tame Scarce Protons and Fast Signal Decay

Author(s):  
Andreas Voskrebenzev ◽  
Jens Vogel‐Claussen
Keyword(s):  
2020 ◽  
Vol 30 (10) ◽  
pp. 5544-5559 ◽  
Author(s):  
Jonathan D Power ◽  
Charles J Lynch ◽  
Babatunde Adeyemo ◽  
Steven E Petersen

Abstract This article advances two parallel lines of argument about resting-state functional magnetic resonance imaging (fMRI) signals, one empirical and one conceptual. The empirical line creates a four-part organization of the text: (1) head motion and respiration commonly cause distinct, major, unwanted influences (artifacts) in fMRI signals; (2) head motion and respiratory changes are, confoundingly, both related to psychological and clinical and biological variables of interest; (3) many fMRI denoising strategies fail to identify and remove one or the other kind of artifact; and (4) unremoved artifact, due to correlations of artifacts with variables of interest, renders studies susceptible to identifying variance of noninterest as variance of interest. Arising from these empirical observations is a conceptual argument: that an event-related approach to task-free scans, targeting common behaviors during scanning, enables fundamental distinctions among the kinds of signals present in the data, information which is vital to understanding the effects of denoising procedures. This event-related perspective permits statements like “Event X is associated with signals A, B, and C, each with particular spatial, temporal, and signal decay properties”. Denoising approaches can then be tailored, via performance in known events, to permit or suppress certain kinds of signals based on their desirability.


2021 ◽  
Vol 2021 (5) ◽  
Author(s):  
M. Ablikim ◽  
◽  
M. N. Achasov ◽  
P. Adlarson ◽  
S. Ahmed ◽  
...  

Abstract The decays D → K−π+π+π− and D → K−π+π0 are studied in a sample of quantum-correlated $$ D\overline{D} $$ D D ¯ pairs produced through the process e+e− → ψ(3770) → $$ D\overline{D} $$ D D ¯ , exploiting a data set collected by the BESIII experiment that corresponds to an integrated luminosity of 2.93 fb−1. Here D indicates a quantum superposition of a D0 and a $$ {\overline{D}}^0 $$ D ¯ 0 meson. By reconstructing one neutral charm meson in a signal decay, and the other in the same or a different final state, observables are measured that contain information on the coherence factors and average strong-phase differences of each of the signal modes. These parameters are critical inputs in the measurement of the angle γ of the Unitarity Triangle in B− → DK− decays at the LHCb and Belle II experiments. The coherence factors are determined to be RK3π = $$ {0.52}_{-0.10}^{+0.12} $$ 0.52 − 0.10 + 0.12 and $$ {R}_{K{\pi \pi}^0} $$ R K ππ 0 = 0.78 ± 0.04, with values for the average strong-phase differences that are $$ {\delta}_D^{K3\pi }=\left({167}_{-19}^{+31}\right){}^{\circ} $$ δ D K 3 π = 167 − 19 + 31 ° and $$ {\delta}_D^{K{\pi \pi}^0}=\left({196}_{-15}^{+14}\right){}^{\circ} $$ δ D K ππ 0 = 196 − 15 + 14 ° , where the uncertainties include both statistical and systematic contributions. The analysis is re-performed in four bins of the phase-space of the D → K−π+π+π− to yield results that will allow for a more sensitive measurement of γ with this mode, to which the BESIII inputs will contribute an uncertainty of around 6°.


Author(s):  
Samar M. Shehata ◽  
Mohamed I. Amin ◽  
El Sayed H. Zidan

Abstract Background Iron deposition distorts the local magnetic field exerting T2* signal decay. Biopsy, serum ferritin, echocardiography are not reliable to adjust iron chelation therapy. Quantified MRI signal decay can replace biopsy to diagnose iron burden, guide treatment, and follow up. The objective of this study is to evaluate the role of T2* in quantification of the liver and heart iron burden in thalassemia major patients. This cross-sectional study included 44 thalassemia patients who were referred to MRI unit, underwent T2* MRI. Results Twenty-one male (47.7%) and 23 female (52.3%) were included (age range 6–15 years, mean age 10.9 ± 2.9 years). Patients with excess hepatic iron show the following: 11/40 (27.5%) mild, (13/40) 32.5% moderate, and (14/40) 35% severe liver iron overload. High statistical significance regarding association between LIC and liver T2* (p = 0.000) encountered. Cardiac T2* values showed no relationship with age (p = 0.6). Conclusion T2* is a good method to quantify, monitor hepatic and myocardial iron burden, guiding chelation therapy and prevent iron-induced cardiac complications.


2014 ◽  
Vol 27 (12) ◽  
pp. 1461-1467 ◽  
Author(s):  
F. C. Horn ◽  
B. A. Tahir ◽  
N. J. Stewart ◽  
G. J. Collier ◽  
G. Norquay ◽  
...  

1990 ◽  
Vol 25 (12) ◽  
pp. 1355
Author(s):  
S. S. Winkler ◽  
Y. H. Kao ◽  
J. A. Sorenson

Sensors ◽  
2018 ◽  
Vol 18 (11) ◽  
pp. 3684 ◽  
Author(s):  
Yesong Gu ◽  
Po-Yuan Tseng ◽  
Xiang Bi ◽  
Jason Yang

The general clinical procedure for viral DNA detection or gene mutation diagnosis following polymerase chain reaction (PCR) often involves gel electrophoresis and DNA sequencing, which is usually time-consuming. In this study, we have proposed a facile strategy to construct a DNA biosensor, in which the platinum electrode was modified with a dual-film of electrochemically synthesized poly(3,4-ethylenedioxythiophene) (PEDOT) resulting in immobilized gold nanoparticles, with the gold nanoparticles easily immobilized in a uniform distribution. The DNA probe labeled with a SH group was then assembled to the fabricated electrode and employed to capture the target DNA based on the complementary sequence. The hybridization efficiency was evaluated with differential pulse voltammetry (DPV) in the presence of daunorubicin hydrochloride. Our results demonstrated that the peak current in DPV exhibited a linear correlation the concentration of target DNA that was complementary to the probe DNA. Moreover, the electrode could be reused by heating denaturation and re-hybridization, which only brought slight signal decay. In addition, the addition of the oxidized form of nicotinamide adenine dinucleotide (NAD+) could dramatically enhance the sensitivity by more than 5.45-fold, and the limit-of-detection reached about 100 pM.


PLoS ONE ◽  
2018 ◽  
Vol 13 (11) ◽  
pp. e0207015 ◽  
Author(s):  
Sourav Bhaduri ◽  
Patricia Clement ◽  
Eric Achten ◽  
Hacene Serrai

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