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1 differently modulated in men and women with Q fever.
2 ver but are lacking in patients with chronic Q fever.
3 a lions may be a risk factor for contracting Q fever.
4 l pathogen responsible for acute and chronic Q fever.
5 ich is associated with a case of human acute Q fever.
6 oonotic bacterial pathogen that causes human Q fever.
7 r bacterium and the causative agent of human Q fever.
8 he design of new generation vaccines against Q fever.
9 d the etiological agent of the human disease Q fever.
10 iella burnetii, the causative agent of human Q fever.
11 the clinical illness seen in human cases of Q fever.
12 he etiological agent of the zoonotic disease Q fever.
13 differential diagnosis of acute and chronic Q fever.
14 lular bacterium and the etiological agent of Q fever.
15 rnetii, the rickettsial organism that causes Q fever.
16 iphospholipid dosages in patients with acute Q fever.
17 sorders have been described in patients with Q fever.
18 4 at the French National Referral Center for Q fever.
19 ith predisposition to development of chronic Q fever.
20 iella burnetii can lead to acute and chronic Q fever.
21 n an increased likelihood to develop chronic Q fever.
22 e bacterium that causes the zoonotic disease Q fever.
23 MYD88 (-938C>A) were associated with chronic Q fever.
24 contribute to the increased risk of chronic Q fever.
25 f developing a peptide mimic vaccine against Q fever.
26 eloping a safe and effective vaccine against Q fever.
28 ar Gram-negative bacterium that causes human Q fever, a flu-like disease that can progress to chronic
30 Coxiella burnetii is the causative agent of Q fever, a zoonotic disease that threatens both human an
31 suspected patient-to-patient transmission of Q fever among pregnant women in a high-risk pregnancy un
32 ellular bacterial pathogen that causes human Q fever, an acute debilitating flu-like illness that can
33 lla burnetii is the bacterial agent of human Q fever, an acute, flu-like illness that can present as
37 a valuable technique in diagnosis of chronic Q fever and during follow-up, often leading to a change
38 nt aortic vegetation in a patient with acute Q fever and high levels of IgG anticardiolipin antibodie
39 were genotyped in 139 patients with chronic Q fever and in 220 controls with cardiovascular risk-fac
40 ligate intracellular bacterium, causes human Q fever and is considered a potential agent of bioterror
43 ntibiotic prophylaxis in patients with acute Q fever and valvulopathy has never been validated in a c
44 important in the pathophysiology of clinical Q fever and/or the induction of protective immunity.
45 ma, were up-regulated in patients with acute Q fever, and the expression levels of the late genes ALO
50 omas are present in patients with resolutive Q fever but are lacking in patients with chronic Q fever
54 Linking a single dairy-goat farm to a human Q-fever cluster, we show widespread transmission, massiv
57 e, we sought to determine how commonly acute Q fever could cause valvular vegetations associated with
58 igate intracellular bacterial agent of human Q fever, Coxiella burnetii, has a remarkable ability to
61 -5% of all acute Q fever infections, chronic Q fever develops, mostly manifesting as endocarditis, in
64 tes of Coxiella burnetii, the cause of human Q fever, display different phenotypes with respect to in
66 fevers for 14 months who was diagnosed with Q fever endocarditis based on an extremely high antibody
67 of clinical and epidemiological features of Q fever endocarditis collected through passive surveilla
73 ults, 9 (1.2%) were considered to have acute Q fever endocarditis, none of whom had a previously know
78 onsidered in the management of patients with Q fever, especially those with persistent focalized infe
79 Coxiella burnetii, the causative agent of Q fever, establishes a unique lysosome-derived intracell
82 uman cases and occurred in a region that was Q-fever free before 2009, providing a unique quasi-exper
83 d in the French National Referral Center for Q fever from January 2007 to December 2011 were included
84 iella burnetii, the causative agent of human Q fever, has been considered a prototypical obligate int
88 haride (LPS), is highly virulent, and causes Q fever in humans and pathology in experimental animals.
89 rRNA gene of Coxiella burnetii, the agent of Q fever in humans, contains an unusually high number of
90 , the etiological agent of acute and chronic Q fever in humans, is a naturally intracellular pathogen
91 Coxiella burnetii, the etiological agent of Q fever in humans, is an intracellular pathogen that rep
94 s is considered to be a late complication of Q fever in patients with preexisting valvular heart dise
97 ignificant disabilities, related to an acute Q fever infection, without other somatic or psychiatric
99 a, Coxiella burnetii, the etiologic agent of Q fever, inhabits a spacious acidified intracellular vac
111 Coxiella burnetii, the etiological agent of Q fever, is a gram-negative obligate intracellular bacte
112 Coxiella burnetii, the causative agent of Q fever, is a human intracellular pathogen that utilizes
113 Coxiella burnetii, the etiological agent of Q fever, is a small, Gram-negative, obligate intracellul
114 Coxiella burnetii, the causative agent of Q fever, is a zoonotic disease with potentially life-thr
116 Coxiella burnetii, the etiological agent of Q fever, is an obligate intracellular bacterium prolifer
118 Growth of Coxiella burnetii, the agent of Q fever, is strictly limited to colonization of a viable
119 were comparable to those seen in human acute Q fever, making this an accurate and valuable animal mod
121 lla burnetii, the etiological agent of human Q fever, occupies a unique niche inside the host cell, w
122 lar survival are poorly defined and a recent Q fever outbreak in the Netherlands emphasizes the need
123 Successful host cell colonization by the Q fever pathogen, Coxiella burnetii, requires translocat
124 ected biomarkers were assessed in blood from Q fever patients by real-time reverse transcription poly
125 An excess risk of DLBCL and FL was found in Q fever patients compared with the general population (S
130 urately identifies patients with low risk of Q fever pneumonia and may help physicians to make more r
131 bjectives were to estimate the prevalence of Q fever pneumonia and to build a prediction rule to iden
132 a prediction rule to identify patients with Q fever pneumonia for empirical antibiotic guidance.
133 -one patients with CAP were included and the Q fever pneumonia prevalence was 24.4% (95% confidence i
134 th a predictive score </=3 had a low risk of Q fever pneumonia with a negative predictive value of 0.
139 ogenesis and genetics and aid development of Q fever preventatives such as an effective subunit vacci
143 ion by Coxiella burnetii, the cause of human Q fever, requires pathogen-directed biogenesis of a larg
145 human patients who had recovered from acute Q fever, respectively, revealed both unique SCV/LCV anti
146 llular pathogens that cause diseases such as Q fever, rickettsioses, brucelloses, tularemia, and othe
147 is, with directed serological testing (i.e., Q fever serology, Bartonella serology) in culture-negati
150 We observed a lymphoma in a patient with Q fever that prompted us to investigate the association
156 single-nucleotide polymorphisms and chronic Q fever were assessed by means of univariate logistic re
160 ll adult Dutch patients suspected of chronic Q fever who were diagnosed since 2007 were retrospective
161 Approximately 20% of patients with acute Q fever will develop chronic fatigue, referred to as Q f
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