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Sensitivity of the chosen measurement protocol was sufficient to measure most of the rat urine samples: only concentrations for glucose and lactate were near or below the LLOQ, especially after treatment with furosemide.
The measurement protocol was as follow: the dried sample was introduced in an empty pan and dried at 150°C during 30 min in order to eliminate moisture.
ERPFref error was estimated with 10%, because the blood sample measurement protocol was identical to [15], showing that errors, usually not higher than 10%, mainly arise from the measurement procedure.
The temperature was then decreased at 1 °C/s to the next temperature and pressure condition with the sample remaining in the HADC, and the measurement protocol was repeated.
An identical measurement protocol was followed after MP placement.
The same measurement protocol was undertaken annually throughout the study.
Similar(34)
Modifications for standardization of the measures and measurement protocol were derived from our previous publication [ 25].
The fact that the used measurement protocol is reliable has been proven in former studies [7, 8].
The measurement protocol is an application of the familiar time-lead analysis that assumes the membrane is presaturated with water.
Due to the relative infancy of the area of 3D dental volume segmentation, with a lack of a gold-standard technique, the need to employ and evaluate segmentation techniques to identify which measurement protocol is most superior is a necessity.
To minimize errors in blood pressure measurement, a standardized measurement protocol is needed.
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