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1 for Lyme disease, giardia, and Valley Fever (coccidioidomycosis).
2 ation of a cellular immune response in human coccidioidomycosis.
3 inclusion in a vaccine candidate to prevent coccidioidomycosis.
4 s as well as from patients with disseminated coccidioidomycosis.
5 ine against C. posadasii in a mouse model of coccidioidomycosis.
6 posadasii) are the causative agents of human coccidioidomycosis.
7 n the donor lungs, leading to posttransplant coccidioidomycosis.
8 be incorporated into a human vaccine against coccidioidomycosis.
9 United States and is the causative agent of coccidioidomycosis.
10 y be useful in the treatment of disseminated coccidioidomycosis.
11 mitis, was investigated in a murine model of coccidioidomycosis.
12 the parental isolate in our murine model of coccidioidomycosis.
13 dies support rAg2/PRA vaccination to prevent coccidioidomycosis.
14 be essential components of a vaccine against coccidioidomycosis.
15 mmitis urease as a candidate vaccine against coccidioidomycosis.
16 e effective therapy for progressive forms of coccidioidomycosis.
17 rational target for therapy of disseminated coccidioidomycosis.
18 t sufficient to make C57BL mice resistant to coccidioidomycosis.
19 munoprotective capacity in a murine model of coccidioidomycosis.
20 nd is a valuable aid in the serodiagnosis of coccidioidomycosis.
21 antigen 2 (Ag2) gene vaccine in experimental coccidioidomycosis.
22 therapy could be used as adjunct therapy for coccidioidomycosis.
23 phic fungal pathogen that causes the disease coccidioidomycosis.
24 PRA as a candidate vaccine for prevention of coccidioidomycosis.
25 s a devastating complication of disseminated coccidioidomycosis.
26 ased the risk for being diagnosed with acute coccidioidomycosis.
27 examining the role of anti-Ag2 antibodies in coccidioidomycosis.
28 in prevention and early recognition of acute coccidioidomycosis.
29 a valuable diagnostic and prognostic aid in coccidioidomycosis.
30 somiasis, histoplasmosis, blastomycosis, and coccidioidomycosis.
31 cavitary pulmonary disease, and disseminated coccidioidomycosis.
32 tibodies and did not meet the definition for coccidioidomycosis.
33 l deaths (95% CrI, 700-1100) associated with coccidioidomycosis.
34 ilitate product development for treatment of coccidioidomycosis.
35 tain immunocompetent patients with pulmonary coccidioidomycosis.
36 r characterization of the natural history of coccidioidomycosis.
37 tigen detection for diagnosis of progressive coccidioidomycosis.
38 ct on outcomes among patients with pulmonary coccidioidomycosis.
39 ngitis (CM) is a devastating complication of coccidioidomycosis.
40 offer improved accuracy for the diagnosis of coccidioidomycosis.
41 olved, and 83% in disseminated and meningeal coccidioidomycosis.
42 gely derived from murine models of pulmonary coccidioidomycosis.
43 r characterization of the natural history of coccidioidomycosis.
44 duced the resistance of B6 mice to pulmonary coccidioidomycosis.
45 involved in MyD88-dependent Th17 immunity to coccidioidomycosis.
46 rst-in-class orphan product for treatment of coccidioidomycosis.
47 ses suggests potential benefit in refractory coccidioidomycosis.
48 e role of V/C salvage therapy for refractory coccidioidomycosis.
49 t report of an epitope-based vaccine against coccidioidomycosis.
50 active or occult infection can also transmit coccidioidomycosis.
51 ccine, are fully protected against pulmonary coccidioidomycosis.
52 immunotherapeutic protocols for treatment of coccidioidomycosis.
53 h prophylaxis did not experience reactivated coccidioidomycosis.
54 ive and IgG-negative EIA result did not have coccidioidomycosis.
55 EIA are thought to have a diagnosis of acute coccidioidomycosis.
56 ts for IgM among persons suspected of having coccidioidomycosis.
57 e in vitro testing of vaccine candidates for coccidioidomycosis.
58 rotects both BALB/c and C57BL/6 mice against coccidioidomycosis.
59 ilitate improved treatment and prevention of coccidioidomycosis.
60 tment course was complicated by disseminated coccidioidomycosis.
61 -month study of patients being evaluated for coccidioidomycosis, 1 or more serum samples were obtaine
62 elve received a diagnosis of acute pulmonary coccidioidomycosis, 17 received other diagnoses, and 17
63 ged > or =60 years with laboratory-confirmed coccidioidomycosis; 2 control groups were selected, the
64 zation (4% vs. 1%, p=0.004) and disseminated coccidioidomycosis (3% vs. 0%, p=0.006) were more freque
67 61 (1.3%) subsequently developed symptomatic coccidioidomycosis; 36/925 (3.9%) had coccidioidomycosis
68 f 47 transplant recipients with a history of coccidioidomycosis, 44 had quiescent infection at transp
70 stomycosis (2.6%), histoplasmosis (5.3%) and coccidioidomycosis (9.4%) than in influenza (18.5%) or p
71 tomycosis (2.6%), histoplasmosis (5.3%), and coccidioidomycosis (9.4%) than in patients with influenz
72 t assays with sera from patients with active coccidioidomycosis, a hyperimmune goat anti-Ag2 serum, a
73 P) antibody present in sera of patients with coccidioidomycosis, a reaction which has been used for s
75 phylaxis effectively suppressed recrudescent coccidioidomycosis after solid organ transplantation for
76 stantially decreased the risk of reactivated coccidioidomycosis after transplantation in these patien
78 action, PBMC from subjects with disseminated coccidioidomycosis also expressed less mRNA for IFN-gamm
80 t of each patient's individual circumstances.Coccidioidomycosis, also known as San Joaquin Valley fev
81 tistically superior efficacy in nonmeningeal coccidioidomycosis, although there is a trend toward sli
83 of this study is to assess the incidence of coccidioidomycosis among lung transplant recipients rece
84 rophylaxis was associated with a low rate of coccidioidomycosis among lung transplant recipients resi
90 /100 000 person-years for histoplasmosis and coccidioidomycosis and 50 cases/100 000 person-years for
91 transplant recipients are at risk of severe coccidioidomycosis and are given prophylaxis to mitigate
92 owed reactivity with sera from patients with coccidioidomycosis and elicited delayed-type footpad hyp
93 Ag nonresponsive patients with disseminated coccidioidomycosis and healthy nonimmune individuals.
94 een used for the diagnosis of other forms of coccidioidomycosis and meningitis caused by other mycose
95 th CD4+ and CD8+ T cells can protect against coccidioidomycosis and that TNF- alpha is a necessary co
96 ts to compare the development of symptomatic coccidioidomycosis and to describe its outcomes for pati
97 romising vaccine candidate for prevention of coccidioidomycosis and warrants further investigation.
98 ibody in 21 (95%) of 22 patients with active coccidioidomycosis and was without reactivity with sera
100 hreshold for histoplasmosis, 69% (35/51) for coccidioidomycosis, and 78% (40/51) for blastomycosis.
102 outcome was the incidence of histoplasmosis, coccidioidomycosis, and blastomycosis for each US county
106 in 5 practices within the areas endemic for coccidioidomycosis (Arizona, California, and Nevada).
107 after antigen stimulation from subjects with coccidioidomycosis as compared to those with another dia
108 be at higher risk for developing symptomatic coccidioidomycosis as compared with those not receiving
110 onse in PBMC from patients with disseminated coccidioidomycosis as well as healthy nonimmune individu
112 omatic coccidioidomycosis; 36/925 (3.9%) had coccidioidomycosis at screening (7, probable infection;
115 ofungin (V/C) salvage therapy for refractory coccidioidomycosis at two children's hospitals between J
116 e respiratory distress syndrome secondary to coccidioidomycosis because of the fear of enhancing fung
117 ed for identifying and managing asymptomatic coccidioidomycosis before patients began TNFi therapy.
120 ar Lv is responsible for early resistance to coccidioidomycosis but not for modulating the IL-10 and
121 cting CF antibody in sera from patients with coccidioidomycosis but was not specific to C. immitis, a
123 ination may be a risk factor for reactivated coccidioidomycosis, but this finding was not statistical
124 dioides sp., the etiological agents of human coccidioidomycosis, but with a travel history including
125 We investigated secondary immunity against coccidioidomycosis by using gene expression microarrays.
129 ctional study developed models incorporating coccidioidomycosis cases reported to the National Notifi
131 Models estimated annual incident symptomatic coccidioidomycosis cases, hospitalizations, and deaths n
132 and March 15, 1994, 203 outbreak-associated coccidioidomycosis cases, including 3 fatalities, were i
137 d in samples from those with acute pulmonary coccidioidomycosis, compared with the other 2 groups (fo
141 on-central nervous system (CNS) disseminated coccidioidomycosis (DCM) has not been previously charact
142 entral nervous system (non-CNS) disseminated coccidioidomycosis (DCM) has not been previously charact
145 blood obtained from patients with pulmonary coccidioidomycosis demonstrated specific cellular immune
147 center to identify factors for recrudescent coccidioidomycosis (despite antifungal prophylaxis) afte
151 patients ages 18-64 with incident pulmonary coccidioidomycosis during 2017-2023 and continuous enrol
153 ecipients who died or received treatment for coccidioidomycosis during the transplant admission, or w
155 variation, and environmental factors impact coccidioidomycosis epidemiology and outcomes in South Am
158 Children's Hospital Central California with coccidioidomycosis from 1 January 2010 to 1 September 20
159 and Drug Administration convened experts in coccidioidomycosis from academia, industry, patient grou
162 Coccidioides posadasii in a murine model of coccidioidomycosis has led to the discovery of potential
164 data suggest that patients with disseminated coccidioidomycosis have a diminished T helper lymphocyte
169 sorbent assays using sera from patients with coccidioidomycosis, histoplasmosis, or blastomycosis.
170 is codes during 2016-2017 for blastomycosis, coccidioidomycosis, histoplasmosis, pneumonia (viral, ba
171 is codes during 2016-2017 for blastomycosis; coccidioidomycosis; histoplasmosis; pneumonia (viral, ba
174 the estimated national burden of symptomatic coccidioidomycosis in 2019 was 10 to 18 times higher tha
175 as defined as laboratory-confirmed, incident coccidioidomycosis in a person infected with HIV for > o
178 (MR) and Dectin-2 in resistance to pulmonary coccidioidomycosis in C57BL/6 (B6) mice and in the inter
180 uary 1995 through 31 June 1997, 153 cases of coccidioidomycosis in human immunodeficiency virus (HIV)
184 ns need to be aware of their higher risk for coccidioidomycosis in order to improve their chances of
187 enic fungus that causes endemic and epidemic coccidioidomycosis in the deserts of North, Central, and
188 cal experience treating medically refractory coccidioidomycosis in the pediatric population with conc
190 rrent epidemics of San Joaquin Valley fever (coccidioidomycosis) in desert regions of the southwester
191 ntal studies indicate that prior symptomatic coccidioidomycosis induces immunity against subsequent i
192 atory distress syndrome owing to a fulminant coccidioidomycosis infection that responded to a short c
210 identification of candidate vaccines against coccidioidomycosis is both efficient and productive.
214 This study suggests that the risk of serious coccidioidomycosis is low among military personnel durin
223 will be unfamiliar with how skin testing for coccidioidomycosis might be useful in patient management
225 Groups were identified as non-disseminated coccidioidomycosis (non-DCM, 462 patients), DCM (44 pati
226 tional recommendations address management of coccidioidomycosis occurring for special at-risk populat
234 nd timing of cases strongly suggest that the coccidioidomycosis outbreak in Ventura County was caused
236 istorical Veterans Affairs (VA)-Armed Forces coccidioidomycosis patient group provides a unique cohor
238 a retrospective study of 531 VA-Armed Forces coccidioidomycosis patients diagnosed between 1955-1958
239 ing the purified rCts1(Ur), 74 out of the 77 coccidioidomycosis patients examined (96.1%) were positi
241 e key topics concerning drug development for coccidioidomycosis presented by speakers and panelists d
242 Northeastern Brazil presents a distinctive coccidioidomycosis profile, with armadillo hunters facin
243 eed for a rapid and safe means of diagnosing coccidioidomycosis prompted us to develop a real-time PC
244 asis to be associated with increased risk of coccidioidomycosis; protease inhibitor therapy was assoc
246 large-volume transplant center in an endemic coccidioidomycosis region to compare outcomes of non-lun
247 eiving other therapies developed symptomatic coccidioidomycosis (relative risk 5.23, 95% confidence i
251 of 0.16 +/- 0.04, patients with disseminated coccidioidomycosis showed a mean response of 0.69 +/- 0.
252 inum, Pleura, Tracheobronchial Tree, Fungus, Coccidioidomycosis, Spherules, Cavity, Nodule, Endemic,
253 of lists of persons with negative serologic coccidioidomycosis tests (laboratory-negative controls,
254 ly higher in DTH-positive donors with active coccidioidomycosis than in healthy, nonimmune controls (
255 d cohort was more likely to have symptomatic coccidioidomycosis than the screened cohort (35/1025 vs
256 sed by all biopsied lesions of patients with coccidioidomycosis that we examined, whether localized t
257 f the 22 men had serologic evidence of acute coccidioidomycosis, the highest attack rate ever reporte
259 ced protective immunity against experimental coccidioidomycosis through the induction of Th1-associat
260 99 and June 2009, 100 patients with previous coccidioidomycosis underwent solid organ transplantation
264 rmation of the importance of B cells against coccidioidomycosis was achieved by demonstrating that va
265 the relative risk of developing symptomatic coccidioidomycosis was calculated in patients with infla
266 Given the patients' lack of recent travel, coccidioidomycosis was not suspected, leading to delays
269 d for 72 h from 8 subjects with disseminated coccidioidomycosis was significantly less than that from
270 going transplantation in an area endemic for coccidioidomycosis, we recommend routine evaluation for
271 are required for vaccine-induced immunity to coccidioidomycosis, we used a temperature-sensitive muta
272 -cause mortality, and mortality secondary to coccidioidomycosis were assessed and compared between gr
273 l-cause mortality and mortality secondary to coccidioidomycosis were assessed and compared between gr
275 idence suggest that 3 individuals with acute coccidioidomycosis were exposed in Washington State, sig
278 tegies, and future diagnostic directions for coccidioidomycosis, which is expected to become more pre
279 ne responses from patients with disseminated coccidioidomycosis who are nonresponsive to coccidioidal
280 a retrospective review of all patients with coccidioidomycosis who underwent solid organ transplanta
281 he medical records of 47 patients with prior coccidioidomycosis who underwent solid organ transplanta
282 s among dogs-which are highly susceptible to coccidioidomycosis, widespread across the US, and have l
283 ent of the ability to control the problem of coccidioidomycosis will require research into the molecu
285 The primary outcome was proven or probable coccidioidomycosis with new asymptomatic seropositivity
286 of TNFi recipients screened for asymptomatic coccidioidomycosis with those of unscreened patients to