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| 1 | Non-invasive neuroimaging using near-infrared light 显示文摘 | STRANGMAN G BOAS D A SUTTON J P | 2002 | Biological Psychia- try2002，52，7： | 1 |
| 2 | Monte Carlo Simulation of Pho- ton Migration in 3D Turbid Media Accelerated by Graphics Processing Units 显示文摘 | Fang Q Boas D A | 2009 | Optics Express2009，17，20： | 1 |
| 3 | Non-invasive neuroimaging using near-infrared light显示文摘 | Strangman G Boas D A Sutton J P | 2002 | Biological Psychiatry2002，52，7： | 1 |
| 4 | Three dimensional Monte Carlo code for photon migration through complex heterogeneous media including the adult human head显示文摘 | Boas D A Culver J P Stott J J | 2002 | Opt Exp2002，10，3： | 1 |
| 5 | Direct object localization and characterization from diffuse photon density wave data显示文摘 | Kilmer M E Miller E L Boas D A | 1999 | Proc SPIE 35971999，4554，： | 1 |
| 6 | Further improvement in reducing superficial contamination in NIRS using double short separation measurements显示文摘 | GAGNON L YCEL M A BOAS D A | 2014 | Neuroimage2014，85，1： | 1 |
| 7 | Monte Carlo simulation of photon mi- gration in 3D turbid media accelerated by graphics process- ing units 显示文摘 | Fang Q Boas D A | 2009 | Optics Express2009，17，20： | 1 |
| 8 | Monte Carlo simulation of photon migration in 3D turbid media accelerated by graphics processing units显示文摘 | FANG Q BOAS D A | | 0，，22： | 1 |
| 9 | Three dimensionalMonte Carlo code for photon migration through complex heterogeneous media including the adult human head显示文摘 | BOAS D A CULVER J P STOTT J J et at | 2001 | Optics Express2001，10，3： | 1 |
| 10 | Non-invasive neuroimaging using near-infrared light 显示文摘 | Strangman G Boas D A Sutton J P | 2002 | Biological Psychiatry2002，52，7： | 1 |
| 11 | Fluorescence lifetime imaging in turbid media显示文摘 | O'Leary M A Boas D A Li X D | 1996 | Optics Letters1996，21，2： | 1 |
| 12 | Monte Carlo simulation of photon migration in 3D turbid media accelerated by graphics processing units 显示文摘 | Q Fang D A Boas | 2009 | Optics Express2009，17，20： | 1 |
| 13 | Active tuberculosis in inflammatory bowel disease patients under treatment from an endemic area in Latin America显示文摘BACKGROUND There has been an increase in cases of inflammatory bowel disease(IBD)in recent years.There is also greater access and availability of immunosuppressive and biological agents,which increase the risk of opportunistic infection despite improving the quality of life and promoting mucosal healing.Tuberculosis(TB)remains a public health problem,and it has a high incidence in several countries.Therefore,knowledge of the risk of developing TB in patients with IBD is important.AIM To evaluate the risk of active TB in patients with IBD under treatment from an endemic area in Latin America.METHODS A standard questionnaire included demographic variables,clinical aspects of IBD disease,history of active TB during treatment,active TB characteristics and evolution,initial screening and results and time from the start of anti-tumor necrosis factor alpha(TNFα)to TB development.RESULTS Azathioprine,anti-TNFα and the combination of these two drugs were associated with a higher risk of active TB incidence.The TNFα blockers increased the relative risk of developing active TB compared to other treatments.All four multivariable models showed that the use of TNFα blockers alone or in combination with azathioprine was an important risk factor for the incidence of active TB.After adjustment for sex,age,type of IBD and latent TB,anti-TNFα with azathioprine increased the relative risk to 17.8 times more than conventional treatment.Late TB,which was diagnosed 3 mo after the start of anti-TNFα,was the most frequent.CONCLUSION Treatment with anti-TNFα increased the risk of active TB in IBD patients from an endemic area in Latin America.This risk was increased when anti-TNFα was combined with azathioprine.The time from the beginning of the treatment to the active TB diagnosis suggests a new TB infection. | Flora Maria Lorenzo Fortes Ney Boa Sorte Victor D Mariano Laila D Andrade Fernanda A Oliveira Monique CA Santos Claudia Ivanilda N dos Santos Catharina A Passos Mila P Pacheco Valdiana C Surlo Neogelia P de Almeida Jaciane AM Fontes Andrea M Pimentel Raquel Rocha Genoile Oliveira Santana | 2020 | World Journal of Gastroenterology2020，26，44： | 1 |
| 14 | Monte Carlo simulation of photon migration in 3D turbid media accelerated by graphics processing units显示文摘 | Fang Q Q Boas D A | | 0，，22： | 1 |
| 15 | Non-invasive neuroimaging using near-infrared light显示文摘 | STRANGMAN G BOAS D A SUTYON J P | 2002 | Biological psychi- atry2002，52，7： | 1 |
| 16 | Three dimensional Monte Carlo code for photon migration through complex heterogeneous media including the adult human head 显示文摘 | Boas D A Culver J P Stott J | 2002 | Opt Exp2002，10，3： | 1 |
| 17 | Tum or-infiltrating macrophageand microvessel density in oral squamous cell carcinoma显示文摘 | Boas D S Takiya C M Gurgel C A | | B r a z Dent J0，24，3： | 1 |
| 18 | Ima- ging the body with diffuse optical tomography 显示文摘 | BOAS D A BROOKS D H MILLER E L | 2001 | IEEE Signal Processing Magazine2001，18，6： | 1 |
| 19 | Twenty years of functional near-infrared spectroscopy: introduc- tion for the special issue显示文摘 | BOAS D A ELWELL C E FERRARI M | 2014 | Neuroimage2014，85，1： | 1 |
| 20 | Diffuse optical reflection tomography with continuous-wave illumination显示文摘 | BOAS D A | 1998 | Optics Express1998，3，3： | 1 |
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