[1] Basurko C,Carles G,Youssef M,et al. Maternal and foetalconsequences of dengue fever during pregnancy [J]. Eur J ObstetGyn R B,2009,147(1):29-32.
[2] 王芹,殷文武,窦丰满,等. 2006年中国登革热疫情监测分析 [J].疾病监测,2009,24(1):22-24.
[3] 李雪莲,武峰,王莹. 登革病毒组织培养技术 [J]. 河南医学研究,2002,11(3):217-219.
[4] 严菊英,卢亦愚,翁景清,等. 浙江省登革热暴发疫情的病原学和分子生物学研究 [J]. 病毒学报,2006,22(5):339-344.
[5] Levi JE,Tateno AF,Machado AF,et al. Evaluation of a commercialreal-time PCR kit for detection of Dengue virus in samples collectedduring an outbreak in Goiania,Central Brazil,in 2005 [J]. J ClinMicrobiol,2007,45(6):1893-1897.
[6] 陈端,谢剑锋,赵珠英,等. 用乳鼠分离及鉴定登革热病毒 [J]. 海峡预防医学杂志,2008,14(6):47-48.
[7] 卢业成,陈万山,张复春,等. 3种登革热抗体检测方法的临床对比研究 [J]. 热带医学杂志,2005,5(5):586-588.
[8] 姜理平,林君芬,龚震宇,等. 间接免疫荧光法检测浙江省输入性登革热疫情 [J]. 中国媒介生物学及控制杂志,2006,17(2):97-98.
[9] Vazquez S,Acosta N,Ruiz D,et al. Immunoglobulin G antibodyresponse in children and adults with acute dengue 3 infection [J]. JVirol Methods,2009,159(1):6-9.
[10] 徐华,郝卫,潘玉先,等.Ⅰ型登革病毒NS1抗原捕获ELISA的建立和初步临床诊断应用 [J]. 中华微生物学和免疫学杂志,2006,26(9):850-854.
[11] Zainah S,Wahab AHA,Mariam M,et al. Performance of acommercial rapid dengue NS1 antigen immunochromatography testwith reference to dengue NS1 antigen-capture ELISA [J]. J VirolMethods,2009,155(2):157-160.
[12] Ramirez AH,Moros Z,Comach G,et al. Evaluation of dengue NS1antigen detection tests with acute sera from patients infected withDengue virus in Venezuela [J]. Diagn Micr Infec Dis,2009,65(3):247-253.
[13] McBride WJH. Evaluation of denude NS1 test kits for the diagnosisof dengue fever [J]. Diagn Micr Infec Dis,2009,64(1):31-36.
[14] 朱玉兰,王佃鹏,甄胜西,等. 登革热病毒RNA实时荧光定量RT-PCR 检测方法的建立 [J]. 热带医学杂志,2009,9(11):1244-1246.
[15] Lai YL,Chung YK,Tan HC,et al. Cost-effective real-time reversetranscriptase PCR(RT-PCR)to screen for Dengue virus followedby rapid single-tube multiplex RT-PCR for serotyping of the virus [J]. J Clin Microbiol,2007,45(3):935-941.
[16] 蒋力云,吴新伟,何丽娟,等. 血清登革热病毒NEST-PCR检测 [J]. 预防医学情报杂志,2006,22(3):265-266.
[17] Klungthong C,Gibbons RV,Thaisomboonsuk B,et al. Dengue virusdetection using whole blood for reverse transcriptase PCR and virusisolation [J]. J Clin Microbiol,2007,45(8):2480-2485.
[18] Das S,Pingle MR,Munoz-Jordán J,et al. Detection and serotypingof Dengue virus in serum samples by multiplex reverse transcriptasePCR-ligase detection reaction assay [J]. J Clin Microbiol,2008,46(10):3276-3284.
[19] Parida M, Horioke K, Ishida H, et al. Rapid detection and differentiationof Dengue virus serotypes by a real-time reverse transcription-loop-mediated isothermal amplification assay [J]. J Clin Microbiol,2005,43(6):2895-2903.
[20] Kang XP,Li YQ,Sun QG,et al. Development of a consensusmicroarray method for identification of some highly pathogenicviruses [J]. J Med Virol,2009,81(11):1945-1950.
[21] 张海燕,马文丽,黄吉城,等. 寡核苷酸芯片技术在甲型流感及登革热病毒检测分型中的初步应用 [J]. 山东医药,2008,48(4):22-23.
[22] Chunhakan S, Butthep P, Yoksan S, et al. Early diagnosis of Denguevirus infection by detection of dengue viral antigen in peripheralblood mononuclear cell [J]. Pediatr Infect Dis J,2009,28(12):1085-1088.
[23] Huhtamo E,Hasu E,Uzcátegui NY,et al. Early diagnosis of denguein travelers:Comparison of a novel real-time RT-PCR,NS1 antigendetection and serology [J]. J Clin Virol,2010,47(1):49-53.
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