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The tumour volume was calculated using the following formula: 0.5 × (shortest diameter)2 × (longest diameter).
Moreover, it has to be pointed out that these particles are the shortest (diameter near to 0.6 μm).
Tumor size was measured daily by caliper, and volume was determined using the following formula: volume = 0.5 × greatest diameter × (shortest diameter)2.
The smallest pore width of the membranes was set at 0.5 nm and the methane and ethane, whose molecular size in the shortest diameter is approximately 0.37 0.38 nm, were chosen as permeating gases.
The area measured by CT is higher than that of echocardiography since the LVOT is ellipsoid and the echocardiography parasternal long axis projection measures the shortest diameter, resulting in underestimation of valve area and overestimation of stenosis.
Tumour size was measured using electronic calipers and tumour volume determined using the calculation: tumour volume = (a 2 × b)/ 2, where a is the shortest diameter and b is the longest diameter of the tumour.
To evaluate the efficacy, sensitivity and specificity of confocal microscopy (CM) parameters: meibomian gland (MG) acinar longest diameter (MGALD), MG acinar shortest diameter (MGASD), inflammatory cell density (ICD), and MG acinar unit density (MGAUD) in the diagnosis of MG dysfunction (MGD).
The longest and shortest diameter of neuronal profiles with a clearly visible nucleus were determined and the average diameter calculated.
(lymph node shortest diameter > 10 mm).
The tumor volume (mm) was estimated by measuring the longest and shortest diameter of the tumor and calculating as follows: volume = (shortest diameter) × (longest diameter) × 3.14/6.
Tumor volume was measured every three days using the formula: (shortest diameter) x longest diameter × 0.5.
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