STROBE is a system that provides object-oriented programming support tools for INTERLISP. It offers a primitive foundation with which more complex structured object representation schemes can be constructed. STROBE implements multiple resident knowledge bases, tangled generalization hierarchies, flexible inheritance of properties, procedural attachment, and event-sensitive procedure invocation.

UNLABELLED BACKGROUND The Consolidated Standards of Reporting Trials (CONSORT) Statement is intended to facilitate better reporting of randomised clinical trials (RCTs). A systematic review recently published in the Cochrane Library assesses whether journal endorsement of CONSORT impacts the completeness of reporting of RCTs; those findings are summarised here. METHODS Evaluations assessin...

The modern-day population is overexposed to visual stimuli accompanied by contrast and strength changes, such as the television or videogames, beginning early in life. These light stimuli may have an influence on the development of the visual system. The purpose of this study was to examine the effects of light stimuli on retinal development. We reared guinea pigs under a daily 12-h strobe ligh...

The “Internet of Things” (IoT) promises ubiquitous, cheap, connected devices. Unfortunately, most of these devices are hastily developed and will never receive code updates. Part of the IoT’s security problem is cryptographic, but established cryptographic solutions seem too heavy or too inflexible to adapt to new use cases. Here we describe Strobe, a new lightweight framework for building both...

BACKGROUND The CONSORT Statement is a reporting guideline for authors when reporting randomized controlled trials (RCTs). It offers a standard way for authors to prepare RCT reports. It has been endorsed by many high-impact medical journals and by international editorial groups. This study was conducted to assess the endorsement of the CONSORT Statement by high-impact medical journals in China ...

BACKGROUND The CONSORT (Consolidated Standards of Reporting Trials) statement was developed by a group of clinical trialists, biostatisticians, epidemiologists and biomedical editors as a means to improve the quality of reports of randomized controlled trials (RCTs). The purpose of the present study is to assess the reporting quality of published RCTs that compare endoscopic carpal tunnel relea...

BACKGROUND We investigated whether there had been an improvement in the quality of reporting for randomised controlled trials of acupuncture and moxibustion published in Chinese journals. We compared the compliance rate for the quality of reporting following the publication of both the STRICTA and CONSORT recommendations in China. METHODS Four Chinese databases were searched for RCTs of acupu...

BACKGROUND Heart failure with preserved ejection fraction (HFpEF) causes significant cardiovascular morbidity and mortality. Current consensus guidelines reflect the neutral results from randomised controlled trials (RCTs). Adequate trial reporting is a fundamental requirement before concluding on RCT intervention efficacy and is necessary for accurate meta-analysis and to provide insight into ...