Time-of-flight scatter rejection in x-ray radiography.

Time-of-flight (TOF) scatter rejection allows for identifying and discarding scattered photons without the use of an anti-scatter grid (ASG). Although TOF scatter rejection was initially presented for cone-beam computed tomography, we propose, herein, to extend this approach to x-ray radiography. This work aims to evaluate with simulations if TOF scatter rejection can outperform ASGs for radiography.

Time-of-flight computed tomography - proof of principle.

Computed tomography has greatly improved over the last decade, especially through x-ray dose exposure reduction while maintaining image quality. Herein, a new concept is proposed to improve the contrast-to-noise ratio (CNR) by including the time-of-flight (TOF) information of individual photons to obtain further insight on the photon's trajectory and to reject scatter contribution. The proof of the concept relies on both simulation and experimental measurements in a cone-beam computed tomography arrangement.

Evaluation of a convenient enzyme immunoassay to assess the quality of genital specimens submitted for the detection of human papillomavirus DNA by consensus PCR.

Background: In the PGMY-line blot assay, a human beta-globin fragment is co-amplified with human papillomavirus (HPV) DNA, and both analytes are detected by hybridization with probes fixed on a strip in a linear array. The beta-globin DIG-MWP test also detects beta-globin amplicons, but in a microtiter plate-based enzyme immunoassay format. Although the PGMY-line blot assay detected 50 cells per test, the beta-globin DIG-MWP test generated a signal above the detection cut-off with five cells per test.

The concentration of immunoreactive prostate specific antigen is not decreased in viscous semen samples.

The concentration of immunoreactive prostate specific antigen (PSA) was determined in the seminal plasma of 79 men who were classified into 4 groups according to sperm characteristics: there were 3 groups with low viscosity sperm (normal, large or small volume) and one group with high viscosity and normal volume. PSA concentrations in the group with high viscosity were not significantly different from the group with low viscosity and normal or large volume. PSA was significantly increased only in the "small volume group" (p less than 0.