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In patients with consecutive FGFR3-positive urine samples the risk of developing a recurrence within 39 months was 90% [ 27].
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Respondents were informed of the purpose of the survey, the procedure for obtaining information and blood samples, the risks and benefits in participation, confidentiality of information collected, and their right to refuse.
Within the study sample, the risk taking sub-scale demonstrated adequate internal consistency reliability (α = 0.68), comparable to values observed with other samples (α = 0.71) (Garner et al., 2007).
In the full sample, the risk of elevated HOMA-IR increased by ∼30% across PD quartiles.
In this longitudinal study of a large national sample, the risk of obesity at 5.5 years of age was not associated with maternal-infant relationship quality.
Drawbacks of this technique include: the manual and individual processing of each individual sample, the risk of contamination, the risk of exposure of laboratory technicians to blood and the high cost [ 19].
Among the other non-smoking profiles in the full sample, the risk of mortality was elevated by between 40%, for non-smoking, physically active, non-drinkers, and 90%, for non-smoking, inactive, non-drinkers.
By assigning one point to each variable and using a score from 0 5 (evaluated within the first 72 hrs of a toxin positive stool sample) the risk of death increased as the score increased.
Interestingly, although prescription opioid misuse is on the rise in North America, in our sample, the risk of HCV acquisition from injection of prescription opioids did not exceed that of traditional street drugs, including heroin, cocaine and crystal methamphetamine.
Specifically, symmetric IUGR appears to be independent of preterm delivery due to PAH exposure in our African-American sample: The risk of symmetric IUGR was significant both among all African-American newborns and among those born full term.
However, they do not take into account the possible risk of a positive MTB culture sample being cross-contaminated with another positive sample, or the risk of a positive sample being contaminated with a (multi- drug resistant multi- drug
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