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چکیده
Findings We found differences of between 20-fold and 60-fold between centres in the prevalence of symptoms of asthma, allergic rhinoconjunctivitis, and atopic eczema, with four-fold to 12-fold variations between the 10th and 90th percentiles for the different disorders. For asthma symptoms, the highest 12-month prevalences were from centres in the UK, Australia, New Zealand, and Republic of Ireland, followed by most centres in North, Central, and South America; the lowest prevalences were from centres in several Eastern European countries, Indonesia, Greece, China, Taiwan, Uzbekistan, India, and Ethiopia. For allergic rhinoconjunctivitis, the centres with the highest prevalences were scattered across the world. The centres with the lowest prevalences were similar to those for asthma symptoms. For atopic eczema, the highest prevalences came from scattered centres, including some from Scandinavia and Africa that were not among centres with the highest asthma prevalences; the lowest prevalence rates of atopic eczema were similar in centres, as for asthma symptoms.
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Explaining Symbolic Trajectory Evaluation by Giving It a Faithful Semantics
Symbolic Trajectory Evaluation (STE) is a formal verification technique for hardware. The current STE semantics is not faithful to the proving power of existing STE tools, which obscures the STE theory unnecessarily. In this paper, we present a new closure semantics for STE which does match the proving power of STE model-checkers, and makes STE easier to understand.
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