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Poor glycemic control was defined as HbA1c > 9%.
Meanwhile, the value for LDH release from untreated cells (negative control) was defined as 0%.
The value for the positive control was defined as 100%; the value for negative control as 0%.
Good glycemic control was defined as 70-180mg/dL in the first 24h postoperatively.
Poor glucose control was defined as HbA1c≥7%; poor blood pressure control as SBP≥130/DBP≥80; and poor lipid control as total cholesterol:HDL ratio≥4.0.
In a further exploratory analysis, optimal control was defined as LDL-C <70 mg per deciliter, HDL-C >50 mg per deciliter, triglycerides <150 mg per deciliter, and SBP/DBP <120/80 mm Hg.
The kinase activity in the vehicle control was defined as 1.
A control was defined as a laboratory-positive patient who did not meet criteria for DHF but was evaluated for thrombocytopenia, plasma leakage and hemorrhage.
A failed positive control was defined as less than 100 sPBMC/106 PBMC in the phytohaemagglutinin (PHA) positive control wells [19].
A control was defined as 1) a participant who continued to be on study medication and 2) last seen within the expected visit window.
Poor glycemic control was defined as A1C of ≥8% (16).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com