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The relationships between pS2 and several clinical and biological parameters were evaluated.
After 3 h the final dose was reached and the biological parameters were evaluated at this time point (referred to as 0 h) and after an additional 2-hour postincubation time at 37°C under submerged conditions (referred to as 2 h).
Similar(58)
Clinical background, preoperative and postoperative echocardiographic parameters were evaluated.
Changes in blood perfusion unit (PU) of pancreatic islet microvascular vasomotion parameters were evaluated.
Various binding parameters were evaluated.
Clinical laboratory parameters were evaluated in blood and urine.
Safety and efficacy parameters were evaluated descriptively.
Pharmacokinetic parameters were evaluated using WinNonLin Software®.
Several clinical and pathological parameters were evaluated.
Descriptive parameters were evaluated non-statistically.
Transcript cleavage and response parameters were evaluated.
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