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To evaluate trends in diminished ovarian reserve (DOR) assignment in the Society for Assisted Reproductive Technology SARTT) Clinic Outcomes Reporting System database and to evaluate its accuracy in predicting poor ovarian response (POR) as defined in European Society of Human Reproduction and Embryology's Bologna criteria (2011).
The reporting system database consists of data from the health institutions, including hospitals and community healthcare centres in cities, and clinical settings (clinics or dispensaries) in rural areas.
37 The national ambulatory care reporting system database details visits to emergency departments, and the Canadian Institute for Health Information discharge abstract database provides information on hospital admissions.
We identified hospital visits from the national ambulatory care reporting system database and the Canadian Institute for Health information discharge abstract database, which contain detailed diagnostic and procedural information on hospital admissions.
The concern regarding the potential for causing cancer is based on the actions of DPP-4 in tumor suppression and the fact that the Food and Drug Administration FDAadverserseventnt reporting system database found an apparent increase in the reports of pancreatitis and pancreatic cancer among patients receiving sitagliptin or exenatide (GLP-1 receptor agonist).
The Vaccine Adverse Event Reporting System database was utilized to conduct a hypothesis testing case-control study by evaluating 3486 total adverse event reports reported following Haemophilus influenza type b (Hib) vaccination.
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We searched the Adverse Events Reporting System, a database of drug side effects maintained by the Food and Drug Administration FDAA).
For example, 17 patients with rheumatoid arthritis developed neurologic events identified from the Adverse Events Reporting System FDA database.
The vaccine adverse event reporting system (VAERS) database was examined for adverse event reports associated with vaccines administered from January 2006 through December 2012 to recipients between 18 and 39 years old with a listed residence in the USA and a specified female gender.
As this was routine epidemiological analysis on the non-nominal data within a standard public-health database reporting system, ethical approval of an institutional review board was not required.
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CEO of Professional Science Editing for Scientists @ prosciediting.com