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| 1 | Identification of phases in zinc alloy powders using electron backscatter diffraction显示文摘 | Martin G Perez Edward A Kenik Matthew J O'Keefe F Scott Miller Benedict Johnson | 2006 | Mater Sci Eng A2006，424，： | 1 |
| 2 | Neurocongnition in depression:patients on and off medication versus healthy comparison subjects显示文摘 | Gualtieri CT Johnson LG Benedict KB | | 0，，： | 1 |
| 3 | Neurocognition in depres- sion patients on and off medication versus healthy comparison sub- jects 显示文摘 | Gualtieri C T Johnson L G Benedict KB | 2006 | J Neuropsyehiatry Clin Neurosei2006，18，2： | 1 |
| 4 | Neurocognition in depression:patients on and off medication versus healthy comparison subjects显示文摘 | Gualtieri C T Johnson L G Benedict K B | 2006 | J Neuropsychiatry Clin Neurosci2006，8，2： | 1 |
| 5 | Neurocognition in depres- sion: patients on and off medication versus healthy comparison sub- jects显示文摘 | Gualtieri CT Johnson LG Benedict KB | 2006 | J Neuropsychiatry Clin Neurosci2006，18，2： | 1 |
| 6 | Neurocognition in depression: patients on and off medication versus healthy comparison subjects 显示文摘 | Gualtieri C T Johnson L G Benedict K B | 2006 | J Neuropsychiatry Clin Neurosci2006，18，2： | 1 |
| 7 | Neurocognition in de pression:patients on and off medication versus healthy com- parison subjeets显示文摘 | Gualtieri CT Johnson LG Benedict KB | 2006 | J Neuropsychiatry Clin Neurosci2006，18，2： | 1 |
| 8 | 显示文摘 | Rivera Berny F Johnson Benedict Y Keefe MatthewJ O' | 2004 | Surface and Coatings Technology2004，176，： | 1 |
| 9 | Neurocognition in depression:patients on and off medication versus healthy comparison subjects显示文摘 | Gualtieri TC Johnson LG Benedict KB | | 0，，： | 1 |
| 10 | Neurocognition in depression:patients on and off medication versus healthy comparison subjects显示文摘 | Gualtieri CT Johnson LG Benedict KB | 2006 | J Neuropsychiatry Clin Neurosci2006，18，2： | 1 |
| 11 | 蒂姆·马洛显示文摘要让金钱来追逐艺术,而非艺术去追逐金钱。
21CBR:如何看待近年来画廊业的生存环境,拍卖行给画廊的压力在增加? | 谭璐 Benedict Johnson | 2014 | 21世纪商业评论2014，，14： | 0 |
| 12 | Probabilistic modeling for an integrated temporary acquired immunity with norovirus epidemiological data显示文摘Integration of acquired immunity into microbial risk assessment for illness incidence is of no doubt essential for the study of susceptibility to illness.In this study,a probabilistic model was set up as dose response for infection and a mathematical derivation was carried out by integrating immunity to obtain probability of illness models.Temporary acquire immunity from epidemiology studies which includes six different Norovirus transmission scenarios such as symptomatic individuals infectious,pre-and post-symptomatic infectiousness(low and high),innate genetic resistance,genogroup 2 type 4 and those with no immune boosting by asymptomatic infection were evaluated.Simulated results on illness inflation factor as a function of dose and exposure indicated that high frequency exposures had immense immunity build up even at high dose levels;hence minimized the probability of illness.Using Norovirus transmission dynamics data,results showed,and immunity included models had a reduction of 2e6 logs of magnitude difference in disease burden for both population and individual probable illness incidence.Additionally,the magnitude order of illness for each dose response remained largely the same for all transmission scenarios;symptomatic infectiousness and no immune boosting after asymptomatic infectiousness also remained the same throughout.With integration of epidemiological data on acquired immunity into the risk assessment,more realistic results were achieved signifying an overestimation of probable risk of illness when epidemiological immunity data are not included.This finding supported the call for rigorous integration of temporary acquired immunity in dose-response in all microbial risk assessments. | Emmanuel de-Graft Johnson Owusu-Ansah Benedict Barnes Robert Abaidoo Hald Tine Anders Dalsgaard Anders Permin Torben Wilde Schou | 2019 | Infectious Disease Modelling2019，4，1： | 0 |
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