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| 1 | Immunologic studies in subjects with a serum sickness-like illness after immunization with human diploid cell rabies vaccine 显示文摘 | Richard J Warrington MB Catheryn J | 1987 | J Allergy Clin Immunol1987，79，4： | 1 |
| 2 | 显示文摘 | Barry J B Liu Da-Wei Catheryn L | 1996 | Polymers for Advanced Technologies1996，7，： | 1 |
| 3 | Epoxy/SiO2 interpenetrating polymer networks显示文摘 | Barry J B Da Wei Liu Catheryn L J | 1996 | Polymers for advanced technologies1996，，7： | 1 |
| 4 | Normal Tissue Complication Probability Analysis of Acute Gastrointestinal Toxicity in Cervical Cancer Patients Undergoing Intensity Modulated Radiation Therapy and Concurrent Cisplatin显示文摘 | Daniel R. Simpson William Y. Song Vitali Moiseenko Brent S. Rose Catheryn M. Yashar Arno J. Mundt Loren K. Mell | 2012 | International Journal of Radiation Oncology Biology Physics2012，，1： | 1 |
| 5 | Effects of freezing and thawing on the microstructure of latex paints显示文摘 | Manish Mittal John A. Roper Catheryn L. Jackson Gregory G. Monaghan Lorraine F. Francis | 2012 | Journal of Colloid And Interface Science2012，，： | 1 |
| 6 | Normal Tissue Complication Probability Modeling of Acute Hematologic Toxicity in Cervical Cancer Patients Treated With Chemoradiotherapy显示文摘 | Brent S. Rose Bulent Aydogan Yun Liang Mete Yeginer Michael D. Hasselle Virag Dandekar Rounak Bafana Catheryn M. Yashar Arno J. Mundt John C. Roeske Loren K. Mell | 2011 | International Journal of Radiation Oncology Biology Physics2011，，3： | 1 |
| 7 | ACR Appropriateness Criteria? on Advanced Cervical Cancer Expert Panel on Radiation Oncology—Gynecology显示文摘 | David K. Gaffney Beth A. Erickson-Wittmann Anuja Jhingran Nina A. Mayr Ajmel A. Puthawala David Moore Gautam G. Rao William Small Mahesh A. Varia Aaron H. Wolfson Catheryn M. Yashar William Yuh Higinia Rosa Cardenes | 2011 | International Journal of Radiation Oncology, Biology, Physics2011，，： | 1 |
| 8 | Dendrimer templates for the formation of gold nanoclusters显示文摘 | GROHN F B AKPALU Y A CATHERYN J L | 2000 | Macromolecules2000，33，16： | 1 |
| 9 | Perinatal transmission in infants of mothers with chronic hepatitis B in California显示文摘AIM To evaluate maternal hepatitis B virus(HBV) DNA as risk for perinatal HBV infection among infants of HBVinfected women in California.METHODS Retrospective analysis among infants born to hepatitis B surface antigen(HBs Ag)-positive mothers who received post vaccination serologic testing(PVST) between 2005 and 2011 in California. Demographic information was collected from the California Department of Public Health Perinatal Hepatitis B Program databaseand matched to birth certificate records. HBV DNA level and hepatitis B e antigen(HBe Ag) status were obtained from three large commercial laboratories in California and provider records if available and matched to mother infant pairs. Univariate analysis compared infected and uninfected infants. Multivariate analysis was restricted to infected infants and controls with complete maternal HBV DNA results using a predefined high HBV DNA level of > 2 × 107 IU/ml,a 5:1 ratio of cases to controls and a two-sided confidence level of 95%.RESULTS A total of 17687 infants were born to HBs Ag positive mothers in California between Jan 1 2005 and Dec 31,2011. Among 11473 infants with PVST,only 125(1.1%) were found to be HBV infected. Among these infected infants,lapses in Advisory Committee on Immunization Practices recommended post exposure prophylaxis(PEP) occurred in only 9 infants. However,PEP errors were not significantly different between infected and uninfected infants. Among the 347 uninfected and infected infants who had maternal HBe Ag and HBV DNA level,case-control analysis found HBe Ag positivity(70.4% vs 28.9%,OR = 46.76,95%CI: 6.05-361.32,P < 0.001) and a maternal HBV DNA level ≥ 2 × 107 IU/ml(92.6% vs 18.5%,OR = 54.5,95%CI: 12.22-247.55,P < 0.001) were associated with perinatal HBV infection. In multivariate logistic regression,maternal HBV DNA level ≥ 2 × 107 IU/ml was the only significant independent predictor of perinatal HBV infection. CONCLUSION In California,transmission is low and most infected infants receive appropriate PEP and vaccination. Maternal HBV DNA ≥ 2 × 107 IU/ml is associated with high risk of perinatal infection. | Jennifer C Burgis Darryl Kong Catheryn Salibay Jennifer Zipprich Kathleen Harriman Samuel So | 2017 | World Journal of Gastroenterology2017，23，27： | 1 |
| 10 | Clinical Outcomes of Intensity-Modulated Pelvic Radiation Therapy for Carcinoma of the Cervix显示文摘 | Michael D. Hasselle Brent S. Rose Joel D. Kochanski Sameer K. Nath Rounak Bafana Catheryn M. Yashar Yasmin Hasan John C. Roeske Arno J. Mundt Loren K. Mell | 2011 | International Journal of Radiation Oncology, Biology, Physics2011，，5： | 1 |
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