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Table 1 Characteristics of included studies Study Design Patients Device Dose and frequency Inclusion criteria Exclusion criteria TMS Sham Richard et al. [39] Randomized, double-blind, sham-controlled 82 82 Portable sTMS over occiput 2 pulses about 30s MA: diagnosis according to ICHD(2 edition) MA: aura > 60 min; metal implants; headache due to trauma or over use of drug.
Here an overview of the approaches taken for LC MS-based metaboLC MS-basedarch is given, describing critical steps in the realisation of such studies: study design and its needs, specific technological problemetabolomicsresearchnd major obstacles is data treatment and biomarker identification.
Box 1 Inclusion criteria for eligible studies Study design: randomised controlled trials and observational studies.
These conflicting results on the meta-analysis are because of a number of included studies, study design, quality of study and adjustment for potential confounding factors.
Clinical studies – study design, classification and etiology of AVN, SC dosage and treatment protocol, incidence of disease progression, patient reported outcomes, volume of necrotic lesion and hip survivorship.
The subgroups defined a priori were, newer versus older studies, study design, mortality versus morbidity outcome, adjustment for smoking, geographic area, and sex.
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Furthermore, among case control studies, study designs have included both hospital-based and population-based studies like ours.
SVD is the secondary investigator; contributed to the conception of the study, study design, and spring design; and overlooked the study and manuscript overview.
Table 2 Summary of studies assessing CMV disease in ICU patients Year of publication Study Study design Patient population Patients no.
AW conceived the study, study design and coordination, article revision.
AH-B participated in drafting the study, study design, and conceiving the study.
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