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This study was determined exempt from institutional review board approval.
Therefore, the ARTP treatment time applied in this study was determined as 40 s.
This study was determined to be exempt by the Institutional Review Board of Massachusetts General Hospital.
Rationale for conducting this study was determined based on a central composite statistical design.
Results show that the method of cephalometric analysis used in this study was determined to be reliable.
The low-field magnetic susceptibility (χ, mass specific) in this study was determined by mass-normalized K m (mean volume susceptibility).
Since there is no complete data on the conservation structures, the P-factor for this study was determined using an alternative method that utilizes slope (Fig. 7) and land cover (Fig. 6) data as suggested by Wischmeier and Smith (1978).
The PZSE of magnetite used in this study was determined using batch titrations with 0.01, 0.05 and 0.1 M NaNO3, and was approximately 5.63, slightly lower than reported PZSE and PZC values of synthetic magnetite, 6.3 6.8 [19, 19, 20].
As described above, FR (mL/mg/2 h) in this study was determined by the 2-h total urine output (mL) following furosemide administration divided by the dose of furosemide (mg).
The surface elemental composition of the adsorbent used in this study was determined using an EDX detector in combination with a field emission scanning electron microscope (Quanta 650 FEG, ESEM-Fa FEI).
The transmission of the Zeiss Plan-Neofluar 63X/1.4 NA objective used in this study was determined to be 0.68.
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