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About 40 percent of children ages 12 to 15 had dental fluorosis, mostly very mild or mild cases, from 1999 to 2004.
Cox proportional hazard models assessed the ability of baseline biomarkers to predict conversion from cognitive normalcy (CDR 0) to very mild or mild dementia (CDR 0.5 and 1).
In addition to the small sample size, this inclusion criterion may have selected against patients who would likely have self-reported very mild or mild disease.
Over a quarter of young people reported pain during botulinum injections; 11% reported very mild or mild pain, 4% moderate pain and 11% severe or very severe pain.
Most programs seek to be able to demonstrate a 25%to33%3% slowing of progression of mild or mild to moderate AD.
Almost half of young people who could self-report and who had received physiotherapy in the previous year reported pain during therapy; 30% reported very mild or mild pain, 9% moderate pain and 6% severe or very severe pain.
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It was diagnosed that 33% of the AGE1 and 64% of the AGE2 Cs users had mild or mild-to-moderate DEs, as confirmed by the anatomic and functional eye probes.
Of the 33 patients with reduced RV function, 8 (24%) had no or minimal, 21 (64%) had mild or mild-to-moderate, and 4 (12%) had moderate or severe TR/PR.
Severity was designated as follows: 0, none: no impairment from or problem with that system; 1, mild: current mild or past significant problem; 2, moderate: impairment interferes with normal activity; 3, severe: severe problems and/or disabling impairment and/or hard-to-control chronic problems; 4, extremely severe: life threatening.
Subsequently, by evaluating a subset of these candidate biomarkers by ELISA, this study validated the utility of four candidate biomarkers for distinguishing groups with mild, very mild, or no dementia (CDR 1, 0.5, 0, respectively).
The Cases were preterm infants who had MRB; that is to say, either isolated or with mild clinical (mild abdominal distention, elevated pre-gavage residuals or emesis) or radiological (intestinal dilatation, mild ileus) signs, different from NEC stage 2 which is characterized by specific radiological signs such as pneumatosis intestinalis [ 3].
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