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10篇 您的检索式:作者名="Debin A"
    题名 作者 年代 出处 被引量
1Purification and characterization of chlorotoxin, a chloride channel ligand from the venom of the scorpion 显示文摘DeBin J A Maggio J E Strichartz G R 1993Am J Physiol1993,264,21:1
2Intranasal immunization with recombinant antigens associated with new cationic particles induces strong mucosal as well as systemic antibody and CTL responses显示文摘Debin A Kravtzoff R Santiago JV 2002Vaccine2002,20,2122:1
3Anti-CD20IgA can protect mice against lymphoma development:evaluation of the direct impact of IgA and cytotoxic effector recruitment on CD20target cells显示文摘Pascal V Laffleur B Debin A 2012Haematologica2012,97,:1
4Intranasal immunization with recombinant antigens associated with new cationic particles induces strong mucosal as well as systemic antibody and CTL responses显示文摘Debin A kravtzoff R Santiago J V 2002Vaccine2002,20,:1
5Intranasal immunization with recombinant antigens associated with new cationic particles induces strong mucosal as well as systemic antibody and CTL responses显示文摘Debin A Kravtzoff R Santiago JV 2002Vaccine2002,20,:1
6Intranasal immunization with recombinant antigens associated with new cationic particles induces strong mucosal as well as systemic antibody and ctl responses显示文摘Debin A Kravtzoff R Santiago JV 2002Vaccine2002,20,2122:1
7Intranasal immunization with recombinant antigens associated with new cationic particles induces strong mucosal as well as systemic antibody and CTL responses显示文摘DEBIN A KRAVTZOFFA R VAZ SANTIAGO J 2002Vaccine2002,20,:1
8Intranasal immunization with recombinant antigens associated with new cationic particles induces strong mucosal as well as systemic antibody and CTL responses 显示文摘Debin A Kravtzoff R Santiago JV 2002Vaccine2002,20,2122:1
9Intranasal immunization with recombinant antigens associated with new cationic particles induces strong mucosal as well as systemic antibody and CTL responses显示文摘Debin A Kravtzoff R Santiago JV 2002Vaccine2002,20,2122:1
10mNGS-based dynamic pathogen monitoring for accurate diagnosis and treatment of severe pneumonia caused by fungal infections显示文摘Metagenomic next-generation sequencing(mNGs)has been widely applied to identify pathogens associated with infectious diseases.However,limited studies have explored the use of mNGs-based dynamic pathogen monitoring in intensive care unit patients with severe pneumonia.Here,we present a clinical case of an 86-year-old male patient with severe pneumonia caused by a fungal infection.During the clinical treatment,four mNGS analyses were performed within two consecutive weeks.Various respiratory fungal pathogens,including Candida orthopsilosis,Candida albicans,and Aspergillus fumigatus were detected by mNGS of bronchoalveolar lavage fluid(BALF).Based on conventional pathogen identification and clinical symptoms,the patient was diagnosed with severe pneumonia caused by a fungal infection.The abundance of fungal species decreased gradually in response to antifungal and empirical therapies,and the fungal infections were effectively con-trolled.In summary,our results demonstrated that mNGS could effectively identify pathogens in patients with severe pneumonia.Additionally,dynamic pathogen monitoring based on mNGS could assist in the precise diag-nosis of complex infections and may facilitate rapid induction of the most appropriate therapy.Zhen Li Changcheng Wu Li-An Tang Yinjie Liang Ruhan A Debin Huang Chuanyi Ning Wenling Wang Wenjie Tan 2023Biosafety and Health2023,5,3:0
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