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1 EBOV-GP vaccine in persons at risk for Ebola virus disease.
2 (TEG) in the management of 2 cases of Ebola virus disease.
3 elae seen in West African survivors of Ebola virus disease.
4 safely provide care for patients with Ebola virus disease.
5 ae persist for more than 2 years after Ebola virus disease.
6 de insight into the pathophysiology of Ebola virus disease.
7 with increased likelihood of confirmed Ebola virus disease.
8 ly used hollow-bore needles, developed Ebola virus disease.
9 and virological follow-up of a case of Ebola virus disease.
10 ort, and investigational therapies for Ebola virus disease.
11 d a wide range of diagnoses other than Ebola virus disease.
12 clinical characteristic for confirmed Ebola virus disease.
13 of these health-care workers developed Ebola virus disease.
14 ied this additional indirect burden of Ebola virus disease.
15 AKI has been observed in cases of Ebola virus disease.
16 e the incubation and latent periods of Ebola virus disease.
17 tic testing of patients with suspected Ebola virus disease.
18 model for severe human respiratory syncytial virus disease.
19 l practice guidelines for acute RRT in Ebola virus disease.
20 required for the care of patients with Ebola virus disease.
21 preventive vaccines to protect against Zika virus disease.
22 aling responses in the pathogenesis of Ebola virus disease.
23 ulate the inflammatory response during Ebola virus disease.
24 odies meeting the case definitions for Ebola virus disease.
25 bola virus disease, Lassa fever, and Marburg virus disease.
26 interferons (IFNs) in animal models of Ebola virus disease.
27 the prevention of laboratory confirmed Ebola virus disease.
28 the confirmation of the first case of Ebola virus disease.
29 clinical development for treatment of Ebola virus disease.
30 stexposure prophylaxis; none developed Ebola virus disease.
31 ases, such as Zika virus infection and Ebola virus disease.
32 and younger with laboratory-confirmed Ebola virus disease admitted to EMCs between June and December
33 t focus has been on the recognition of Ebola virus disease among travelers from West Africa, cases of
34 manifestations and adverse outcomes of Zika virus disease among travelers infected in the Americas a
35 manifestations and adverse outcomes of Zika virus disease among travelers infected in the Americas a
37 or use of post-exposure prophylaxis in Ebola virus disease and identify the priorities for future pre
38 Because of the overlap of symptoms of Ebola virus disease and malaria, the care delivery of malaria
39 98) and age-matched patients with acute Zika virus disease and no neurological symptoms (control grou
40 o decrease the risk of transmission of Ebola virus disease and report pilot data demonstrating no det
41 the four prefectures most affected by Ebola virus disease and selected four randomly from prefecture
42 cination platform in a rodent model of Ebola virus disease and that GP1 N-glycan loss does not influe
43 e information about the pathogenesis of Zika virus disease and the mechanism by which candidate preve
46 hly efficacious and safe in preventing Ebola virus disease, and is most likely effective at the popul
47 re and symptoms of sexually transmitted Zika virus disease, and results of semen testing for Zika vir
49 r experience of treating patients with Ebola virus disease at Emory University in the United States.
50 cohort study, consecutive survivors of Ebola virus disease attending Kerry Town survivor clinic (Free
52 mbination increased the probability of Ebola virus disease by 3.2-fold (95% CI 2.3-4.4), but the sens
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
58 clinical characteristics of suspected Ebola virus disease cases admitted to Connaught Hospital's Ebo
60 e subsequently classified as confirmed Ebola virus disease cases or non-cases according to the result
61 oup analysis, 15 (9%) of 161 confirmed Ebola virus disease cases reported neither a history of fever
64 tion of health consequences related to Ebola virus disease could improve patient care for survivors a
65 pitalization of the first patient with Ebola virus disease diagnosed in the United States on 28 Septe
66 assays and the urgent need for a rapid Ebola virus disease diagnosis precluded development of validat
68 Inadequate access to rapid testing for Ebola virus disease during the 2014-to-2016 outbreak led to an
69 arch 2016, the West Africa epidemic of Ebola virus disease (Ebola) had resulted in a total of 28,646
70 In 2014, a major epidemic of human Ebola virus disease emerged in West Africa, where human-to-hum
71 dicator across three time periods: pre-Ebola virus disease epidemic (January, 2013, to February, 2014
73 vaccines could help to end the ongoing Ebola virus disease epidemic in parts of west Africa, and miti
75 work were delayed for months until the Ebola virus disease epidemic was officially declared an emerge
76 case management in the context of the Ebola-virus-disease epidemic and document the effect of the Eb
79 elivery of malaria care because of the Ebola-virus-disease epidemic threatens malaria control in Guin
82 and renal failure may occur in severe Ebola virus disease, especially in patients burdened with high
84 n the characteristics of patients with Ebola virus disease (EVD) and clinical management of EVD in se
85 lth, trauma, and personal exposures to Ebola virus disease (EVD) and health behaviors in post-conflic
86 rsonnel (HCP) caring for patients with Ebola virus disease (EVD) are at increased risk for infection
87 Animal models recapitulating human Ebola virus disease (EVD) are critical for insights into virus
88 e current West African outbreak of the Ebola virus disease (EVD) began in Guinea in December 2013 and
92 2014 and February 2015, the number of Ebola virus disease (EVD) cases reported in Sierra Leone decli
94 ned dramatically, sporadic clusters of Ebola virus disease (EVD) continue well beyond the double incu
110 sticks of patients suspected of having Ebola virus disease (EVD) for field diagnostics during an outb
111 ans to manage a patient with confirmed Ebola virus disease (EVD) for the full duration of illness and
112 m the 2013-16 west African outbreak of Ebola virus disease (EVD) has raised several new issues: long-
115 nical and virologic characteristics of Ebola virus disease (EVD) in children have not been thoroughly
120 In the wake of the recent outbreak of Ebola virus disease (EVD) in several African countries, the Wo
121 scent plasma (CP) for the treatment of Ebola virus disease (EVD) in the current outbreak, predominant
124 emen of a large number of survivors of Ebola virus disease (EVD) in Western Africa may contribute to
125 aracterize epidemiological patterns of Ebola virus disease (EVD) infections during the West African 2
131 apid, accurate, and early diagnosis of Ebola virus disease (EVD) is critical to public health contain
138 , all known transmission chains of the Ebola virus disease (EVD) outbreak in west Africa had been sto
140 int-of-care instruments in the ongoing Ebola virus disease (EVD) outbreak in West Africa would have d
145 present, there is a major emphasis on Ebola virus disease (EVD) preparedness training at medical fac
146 The unprecedented 2014 epidemic of Ebola virus disease (EVD) prompted an international response t
148 The 2013-2015 West African epidemic of Ebola virus disease (EVD) reminds us of how little is known ab
149 persistence in asymptomatic humans and Ebola virus disease (EVD) sequelae have emerged as significant
153 unparalleled West African outbreak of Ebola virus disease (EVD) that began in late 2013, the lack of
155 l transmission from a male survivor of Ebola virus disease (EVD) to his female partner (the patient i
156 (EMLab) consortium was deployed to the Ebola virus disease (EVD) treatment unit in Gueckedou, Guinea,
157 ty and efficacy of vaccines to prevent Ebola virus disease (EVD) were unknown when the incidence of E
160 as been developed for the treatment of Ebola virus disease (EVD), but its efficacy and safety in huma
164 than 30 000 individuals have acquired Ebola virus disease (EVD), the medical and scientific communit
172 ction of nonhuman primates from deadly Ebola virus disease, even when treatment was begun as late as
173 history of fever and risk factors for Ebola virus disease exposure do not have sufficient sensitivit
175 e selection of patients with suspected Ebola virus disease for admission by identifying presenting cl
176 nd therapy development, and control of Ebola virus disease for noninfectious disease physicians.
177 ccination group there were 16 cases of Ebola virus disease from seven clusters, showing a vaccine eff
180 e limited data available for long-term Ebola virus disease health outcomes suggest that sequelae pers
181 We regarded samples to be positive for Ebola virus disease if the cycle threshold was 40 or lower.
182 ytokine response that is a hallmark of Ebola virus disease.IMPORTANCE Understanding how the host resp
183 vaccination trial, suspected cases of Ebola virus disease in Basse-Guinee (Guinea, west Africa) were
184 the effect of rVSV-ZEBOV in preventing Ebola virus disease in contacts and contacts of contacts of re
185 ary analysis compared the incidence of Ebola virus disease in eligible and vaccinated individuals ass
186 protocol and compared the incidence of Ebola virus disease in eligible and vaccinated individuals in
193 vided no benefit for the prevention of Ebola virus disease in rhesus macaques with regards to reducti
194 provision of care of two patients with Ebola virus disease in the biocontainment unit at the Universi
195 alence and severity of respiratory syncytial virus disease in the first few weeks of life, whereas ma
196 ical manifestations and epidemiology of Zika virus disease in travelers exposed in the Americas.
197 ical manifestations and epidemiology of Zika virus disease in travelers exposed in the Americas.
202 CT]) for all contacts of patients with Ebola virus disease (in terms of administration and averted ET
204 For an SWCT, regional variation in Ebola virus disease incidence trends produced increased false-
205 and 26% for an SWCT, depending on the Ebola virus disease incidence within the trial population.
206 the provision of care to patients with Ebola virus disease, including absence of pre-existing isolati
207 ed for the prevention and treatment of Ebola virus disease, including following a potentially high-ri
209 and June 16, 2015, of 151 survivors of Ebola virus disease invited to participate, 112 (74%) provided
213 n Sierra Leone, where the incidence of Ebola virus disease is spatiotemporally heterogeneous, and is
215 ica, Crimean-Congo haemorrhagic fever, Ebola virus disease, Lassa fever, and Marburg virus disease.
216 In the severe form, patients with Ebola virus disease may require life-sustaining therapy, inclu
217 n medically evacuated for treatment of Ebola virus disease, more commonly they were evacuated after p
219 l 117 clusters showed that no cases of Ebola virus disease occurred 10 days or more after randomisati
224 n Freetown were screened for suspected Ebola virus disease on arrival and, if necessary, were admitte
226 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
241 ulation level when delivered during an Ebola virus disease outbreak via a ring vaccination strategy.
243 ublic health officials when addressing Ebola virus disease outbreaks in countries and seasons where m
246 escription of the clinical features of Ebola virus disease over the duration of illness in children a
248 critical role for the delta peptide in Ebola virus disease pathology and as a possible target for nov
249 t may be a novel, targetable aspect of Ebola virus disease pathology.IMPORTANCE During the unparallel
250 pment (PPE) during care activities for Ebola virus disease patients has not yet been characterized.
251 The 2014 west African epidemic of Ebola virus disease posed a major threat to the health systems
253 es from 106 individuals with suspected Ebola virus disease presenting at two clinical centres in Sier
258 fe and effective care of patients with Ebola virus disease requires significant communication and pla
262 dengue, chikungunya, yellow fever, and Zika virus disease) resulting from the triad of the modern wo
263 e, or clinically suspected diagnosis of Zika virus disease seen between January 2013 and 29 February
264 e, or clinically suspected diagnosis of Zika virus disease seen between January 2013 and 29 February
266 treatment to contacts of patients with Ebola virus disease should be considered by public health offi
271 Health Screening Program (MHSP) offers Ebola virus disease survivors semen testing for Ebola virus.
272 's Health Screening Program helps male Ebola virus disease survivors understand their individual risk
274 n the concern about potentially lethal Ebola virus disease, the patient was offered, and provided his
275 y and clinical data from patients with Ebola virus disease to better inform clinical management algor
276 tment to all contacts of patients with Ebola virus disease, to prevent the onset of febrile malaria a
277 quent renal recovery in a patient with Ebola virus disease treated at Emory University Hospital, in A
279 n of ACTs to contacts of patients with Ebola virus disease was cost saving for contacts of all ages i
280 , the characteristic histopathology of Ebola virus disease was not observed, and this absence of seve
283 m optimal care in a future outbreak of Ebola virus disease, we employed the Grading of Recommendation
284 c 8, 2014, 850 patients with suspected Ebola virus disease were admitted to the holding unit, of whom
289 rVSVDeltaG-ZEBOV-GP vaccine prevented Ebola virus disease when used at 2 x 107 plaque-forming units
291 ents, alive on arrival, with confirmed Ebola virus disease who were admitted to the Kerry Town Ebola
292 s report describes three patients with Ebola virus disease who were treated in the United States and
293 ributed to our better understanding of Ebola virus disease with a paper underlying the crucial role o
294 atient who had been treated for severe Ebola virus disease with high viral load (peak cycle threshold
295 ome was a laboratory confirmed case of Ebola virus disease with onset 10 days or more from randomisat
296 imary outcome was laboratory-confirmed Ebola virus disease with onset of symptoms at least 10 days af
297 cination group, there were no cases of Ebola virus disease with symptom onset at least 10 days after
298 offers substantial protection against Ebola virus disease, with no cases among vaccinated individual
299 offers substantial protection against Ebola virus disease, with no cases among vaccinated individual
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