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1 EBOV-GP vaccine in persons at risk for Ebola virus disease.
2 preventive vaccines to protect against Zika virus disease.
3 ulate the inflammatory response during Ebola virus disease.
4 odies meeting the case definitions for Ebola virus disease.
5 bola virus disease, Lassa fever, and Marburg virus disease.
6 interferons (IFNs) in animal models of Ebola virus disease.
7 the prevention of laboratory confirmed Ebola virus disease.
8 the confirmation of the first case of Ebola virus disease.
9 clinical development for treatment of Ebola virus disease.
10 cted non-human primates (NHPs) against Ebola virus disease.
11 stexposure prophylaxis; none developed Ebola virus disease.
12 ases, such as Zika virus infection and Ebola virus disease.
13 (TEG) in the management of 2 cases of Ebola virus disease.
14 rst licensed vaccine for prevention of Ebola virus disease.
15 elae seen in West African survivors of Ebola virus disease.
16 safely provide care for patients with Ebola virus disease.
17 ae persist for more than 2 years after Ebola virus disease.
18 s are the most common complications of Ebola virus disease.
19 de insight into the pathophysiology of Ebola virus disease.
20 with increased likelihood of confirmed Ebola virus disease.
21 ly used hollow-bore needles, developed Ebola virus disease.
22 and virological follow-up of a case of Ebola virus disease.
23 ort, and investigational therapies for Ebola virus disease.
24 d a wide range of diagnoses other than Ebola virus disease.
25 clinical characteristic for confirmed Ebola virus disease.
26 may contribute to the severity of influenza virus disease.
27 uld play a role in vaccination against Ebola virus disease.
28 o inflammation during human immunodeficiency virus disease.
29 accine (FILORAB3) to protect against Marburg virus disease.
30 or the efficient monitoring and treatment of virus diseases.
31 approved drugs to treat both Lassa and Ebola virus diseases.
32 ical signs and symptoms associated with Zika virus disease, 133 (94%) children had rash, 104 (74%) fe
36 and younger with laboratory-confirmed Ebola virus disease admitted to EMCs between June and December
37 t focus has been on the recognition of Ebola virus disease among travelers from West Africa, cases of
38 manifestations and adverse outcomes of Zika virus disease among travelers infected in the Americas a
39 manifestations and adverse outcomes of Zika virus disease among travelers infected in the Americas a
40 or use of post-exposure prophylaxis in Ebola virus disease and identify the priorities for future pre
41 98) and age-matched patients with acute Zika virus disease and no neurological symptoms (control grou
42 o decrease the risk of transmission of Ebola virus disease and report pilot data demonstrating no det
43 cination platform in a rodent model of Ebola virus disease and that GP1 N-glycan loss does not influe
45 e information about the pathogenesis of Zika virus disease and the mechanism by which candidate preve
46 was high in people who recovered from Ebola virus disease and were discharged from Ebola treatment u
48 re and symptoms of sexually transmitted Zika virus disease, and results of semen testing for Zika vir
50 cohort study, consecutive survivors of Ebola virus disease attending Kerry Town survivor clinic (Free
52 ed by recognizing the fascinating puzzles of virus diseases, being in good places at the right time,
53 , most assays used in the detection of Ebola virus disease by more than 44 diagnostic laboratories yi
54 ll 28 patients who tested positive for Ebola virus disease by RT-PCR were also positive by fingerstic
61 tion of health consequences related to Ebola virus disease could improve patient care for survivors a
62 assays and the urgent need for a rapid Ebola virus disease diagnosis precluded development of validat
64 Inadequate access to rapid testing for Ebola virus disease during the 2014-to-2016 outbreak led to an
65 arch 2016, the West Africa epidemic of Ebola virus disease (Ebola) had resulted in a total of 28,646
66 In 2014, a major epidemic of human Ebola virus disease emerged in West Africa, where human-to-hum
67 dicator across three time periods: pre-Ebola virus disease epidemic (January, 2013, to February, 2014
71 work were delayed for months until the Ebola virus disease epidemic was officially declared an emerge
73 case management in the context of the Ebola-virus-disease epidemic and document the effect of the Eb
75 cells from four survivors treated for Ebola virus disease (EVD) 1 or 3 months after discharge from t
78 n the characteristics of patients with Ebola virus disease (EVD) and clinical management of EVD in se
79 lth, trauma, and personal exposures to Ebola virus disease (EVD) and health behaviors in post-conflic
80 l hemorrhagic fevers (VHFs), including Ebola virus disease (EVD) and Lassa fever (LF), highlight the
81 rsonnel (HCP) caring for patients with Ebola virus disease (EVD) are at increased risk for infection
82 Animal models recapitulating human Ebola virus disease (EVD) are critical for insights into virus
84 e current West African outbreak of the Ebola virus disease (EVD) began in Guinea in December 2013 and
86 occurrence of previously undocumented Ebola virus disease (EVD) cases and infections, and to reconst
88 ned dramatically, sporadic clusters of Ebola virus disease (EVD) continue well beyond the double incu
90 we developed a compartmental model for Ebola virus disease (EVD) dynamics, which includes three diffe
101 sticks of patients suspected of having Ebola virus disease (EVD) for field diagnostics during an outb
102 ans to manage a patient with confirmed Ebola virus disease (EVD) for the full duration of illness and
103 m the 2013-16 west African outbreak of Ebola virus disease (EVD) has raised several new issues: long-
104 several experimental therapeutics for Ebola virus disease (EVD) have been developed, the safety and
108 nical and virologic characteristics of Ebola virus disease (EVD) in children have not been thoroughly
110 didates.IMPORTANCE The pathogenesis of Ebola virus disease (EVD) in humans is complex, and the mechan
112 In the wake of the recent outbreak of Ebola virus disease (EVD) in several African countries, the Wo
113 scent plasma (CP) for the treatment of Ebola virus disease (EVD) in the current outbreak, predominant
114 y being used to combat the outbreak of Ebola virus disease (EVD) in the Democratic Republic of the Co
118 emen of a large number of survivors of Ebola virus disease (EVD) in Western Africa may contribute to
120 aracterize epidemiological patterns of Ebola virus disease (EVD) infections during the West African 2
127 apid, accurate, and early diagnosis of Ebola virus disease (EVD) is critical to public health contain
133 c information at the start of the 2018 Ebola virus disease (EVD) outbreak in North Kivu Province.
135 , all known transmission chains of the Ebola virus disease (EVD) outbreak in west Africa had been sto
136 int-of-care instruments in the ongoing Ebola virus disease (EVD) outbreak in West Africa would have d
140 of the Congo (DRC) recorded its eighth Ebola virus disease (EVD) outbreak, approximately 3 years afte
141 e late phase of the large West-African Ebola virus disease (EVD) outbreak, the majority of patients w
143 The unprecedented 2014 epidemic of Ebola virus disease (EVD) prompted an international response t
145 persistence in asymptomatic humans and Ebola virus disease (EVD) sequelae have emerged as significant
147 In this study, serum antibodies from Ebola virus disease (EVD) survivors from Sierra Leone were pro
150 ditory, and visual complications among Ebola Virus Disease (EVD) survivors; however, little is known
151 unparalleled West African outbreak of Ebola virus disease (EVD) that began in late 2013, the lack of
153 trials and used to treat patients with Ebola virus disease (EVD) toward the end of the epidemic.
154 (EMLab) consortium was deployed to the Ebola virus disease (EVD) treatment unit in Gueckedou, Guinea,
156 ty and efficacy of vaccines to prevent Ebola virus disease (EVD) were unknown when the incidence of E
159 as been developed for the treatment of Ebola virus disease (EVD), but its efficacy and safety in huma
161 For highly contagious diseases such as Ebola virus disease (EVD), interpersonal contact plays the mos
162 than 30 000 individuals have acquired Ebola virus disease (EVD), the medical and scientific communit
163 ce of subclinical and paucisymptomatic Ebola Virus Disease (EVD), the prevalence and associated risk
165 ontributor to outcome in patients with Ebola virus disease (EVD), with high values leading to a fatal
166 frequently recommended intervention in Ebola virus disease (EVD), yet its impact on patient outcomes
180 history of fever and risk factors for Ebola virus disease exposure do not have sufficient sensitivit
181 ccination group there were 16 cases of Ebola virus disease from seven clusters, showing a vaccine eff
182 neral Guinean population, survivors of Ebola virus disease had a more than five-times increased risk
186 We regarded samples to be positive for Ebola virus disease if the cycle threshold was 40 or lower.
187 gans contributes to the development of Ebola virus disease.IMPORTANCE Ebola virus (EBOV) remains a hi
188 is a promising vaccine candidate for Marburg virus disease.IMPORTANCE Marburg virus (MARV) is a virus
189 ytokine response that is a hallmark of Ebola virus disease.IMPORTANCE Understanding how the host resp
190 the effect of rVSV-ZEBOV in preventing Ebola virus disease in contacts and contacts of contacts of re
191 ary analysis compared the incidence of Ebola virus disease in eligible and vaccinated individuals ass
192 protocol and compared the incidence of Ebola virus disease in eligible and vaccinated individuals in
199 vided no benefit for the prevention of Ebola virus disease in rhesus macaques with regards to reducti
200 alence and severity of respiratory syncytial virus disease in the first few weeks of life, whereas ma
201 ical manifestations and epidemiology of Zika virus disease in travelers exposed in the Americas.
202 ical manifestations and epidemiology of Zika virus disease in travelers exposed in the Americas.
208 CT]) for all contacts of patients with Ebola virus disease (in terms of administration and averted ET
209 For an SWCT, regional variation in Ebola virus disease incidence trends produced increased false-
210 the provision of care to patients with Ebola virus disease, including absence of pre-existing isolati
212 and June 16, 2015, of 151 survivors of Ebola virus disease invited to participate, 112 (74%) provided
217 n Sierra Leone, where the incidence of Ebola virus disease is spatiotemporally heterogeneous, and is
218 ica, Crimean-Congo haemorrhagic fever, Ebola virus disease, Lassa fever, and Marburg virus disease.
219 the mechanisms of evolution is important for virus disease management and controlling the emergence o
220 o-friendly strategies is required to advance virus disease management in diverse agricultural croppin
221 showed therapeutic efficacy in this Marburg virus disease model with treatment initiation 5 days pos
222 n medically evacuated for treatment of Ebola virus disease, more commonly they were evacuated after p
225 identified in a human survivor of Bundibugyo virus disease, neutralizes both Bundibugyo virus and Ebo
226 l 117 clusters showed that no cases of Ebola virus disease occurred 10 days or more after randomisati
230 sought to quantify the consequences of Ebola virus disease on maternal and child health services in t
238 at a human survivor of the 1995 Kikwit Ebola virus disease outbreak maintained circulating antibodies
242 geting EBOV.IMPORTANCE The most recent Ebola virus disease outbreak, from 2014 to 2016, resulted in a
243 been historically used to investigate Ebola virus disease outbreaks and how new technologies allow f
244 ublic health officials when addressing Ebola virus disease outbreaks in countries and seasons where m
246 tion that has been applied to Ebola and Zika virus disease outbreaks, among others, and is currently
248 escription of the clinical features of Ebola virus disease over the duration of illness in children a
249 r safe and effective vaccines against dengue virus disease, particularly for individuals who are deng
251 critical role for the delta peptide in Ebola virus disease pathology and as a possible target for nov
252 t may be a novel, targetable aspect of Ebola virus disease pathology.IMPORTANCE During the unparallel
253 pment (PPE) during care activities for Ebola virus disease patients has not yet been characterized.
254 The 2014 west African epidemic of Ebola virus disease posed a major threat to the health systems
258 dengue, chikungunya, yellow fever, and Zika virus disease) resulting from the triad of the modern wo
259 e, or clinically suspected diagnosis of Zika virus disease seen between January 2013 and 29 February
260 e, or clinically suspected diagnosis of Zika virus disease seen between January 2013 and 29 February
262 treatment to contacts of patients with Ebola virus disease should be considered by public health offi
268 Health Screening Program (MHSP) offers Ebola virus disease survivors semen testing for Ebola virus.
269 's Health Screening Program helps male Ebola virus disease survivors understand their individual risk
270 virus, despite never having developed Ebola virus disease symptoms, highlighting an important and po
271 most commonly reported symptom of post-Ebola virus disease syndrome in survivors is arthralgia, yet i
273 y and clinical data from patients with Ebola virus disease to better inform clinical management algor
274 tment to all contacts of patients with Ebola virus disease, to prevent the onset of febrile malaria a
275 n of ACTs to contacts of patients with Ebola virus disease was cost saving for contacts of all ages i
276 , the characteristic histopathology of Ebola virus disease was not observed, and this absence of seve
279 m optimal care in a future outbreak of Ebola virus disease, we employed the Grading of Recommendation
280 c 8, 2014, 850 patients with suspected Ebola virus disease were admitted to the holding unit, of whom
286 efit could be obtained.Twelve cases of Nipah virus disease were treated in the emergency department o
287 rVSVDeltaG-ZEBOV-GP vaccine prevented Ebola virus disease when used at 2 x 107 plaque-forming units
289 to gain information about survivors of Ebola virus disease who subsequently died from their closest f
290 contact and follow-up all survivors of Ebola virus disease who were discharged from Ebola treatment u
292 ributed to our better understanding of Ebola virus disease with a paper underlying the crucial role o
293 atient who had been treated for severe Ebola virus disease with high viral load (peak cycle threshold
294 ome was a laboratory confirmed case of Ebola virus disease with onset 10 days or more from randomisat
295 cination group, there were no cases of Ebola virus disease with symptom onset at least 10 days after
296 offers substantial protection against Ebola virus disease, with no cases among vaccinated individual
297 offers substantial protection against Ebola virus disease, with no cases among vaccinated individual
298 ed surveillance systems for symptomatic Zika virus disease (ZVD) and birth defects provided complemen