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1 us, idiopathic pulmonary fibrosis and dengue haemorrhagic fever).
2 s: filamentous, enveloped viruses that cause haemorrhagic fever.
3 ging pathogens and causative agents of viral haemorrhagic fever.
4 usly efficient vectors of malaria and Dengue haemorrhagic fever.
5 arburg filoviruses cause deadly outbreaks of haemorrhagic fever.
6 s a model for the treatment of ZEBOV-induced haemorrhagic fever.
7 rmly lethal non-human primate model of ZEBOV haemorrhagic fever.
8 ephalitis, Kyasanur Forest disease, and Omsk haemorrhagic fever.
9 rovides a paradigm for the treatment of MARV haemorrhagic fever.
10 loped clinical symptoms consistent with MARV haemorrhagic fever.
11 respiratory syndrome), avian influenza, and haemorrhagic fever.
12 (rVSV), as a postexposure treatment for MARV haemorrhagic fever.
13 athway could ameliorate the effects of Ebola haemorrhagic fever.
14 lance and response capacity to contain viral haemorrhagic fevers.
15 haemorrhagic fever in man, designated Ebola haemorrhagic fever, and are endemic in regions of centra
16 onse syndromes in bacterial sepsis and viral haemorrhagic fevers, and anticoagulants can be effective
21 haemorrhagic fevers in Africa, Crimean-Congo haemorrhagic fever, Ebola virus disease, Lassa fever, an
23 nd Marburg filoviruses cause a rapidly fatal haemorrhagic fever in humans for which no approved antiv
25 e causative agents of a severe form of viral haemorrhagic fever in man, designated Ebola haemorrhagic
26 ubnational pandemic potential for four viral haemorrhagic fevers in Africa, Crimean-Congo haemorrhagi
30 vary within Africa, with regions where viral haemorrhagic fever outbreaks have previously occurred (e
33 ses like Rift Valley fever and Crimean-Congo haemorrhagic fever viruses continue to emerge in new geo
34 arito, Junin and Sabia viruses are New World haemorrhagic fever viruses that do not use alpha-dystrog
35 of tick-borne encephalitis and Crimean-Congo haemorrhagic fever viruses, have changed their geographi
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