コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ncy were reclassified as benign (thymoma and histoplasmosis).
2 is, chronic herpes simplex, and disseminated histoplasmosis).
3 ncover how innate immunity modulation alters histoplasmosis.
4 nction, resulting in an inability to control histoplasmosis.
5 e existence a regulatory IL-17/IL-23 axis in histoplasmosis.
6 ectious complications including disseminated histoplasmosis.
7 y represents a strategy of immunotherapy for histoplasmosis.
8 capsulatum, a pathogenic fungus that causes histoplasmosis.
9 ct on host resistance in mice with secondary histoplasmosis.
10 aling has on host defenses against pulmonary histoplasmosis.
11 The same is true for histoplasmosis.
12 surgery, one had arm cellulitis, and one had histoplasmosis.
13 IL-4 in the lung on the course of pulmonary histoplasmosis.
14 and mycological tests to accurately diagnose histoplasmosis.
15 , subverted protective immunity in secondary histoplasmosis.
16 rapy are at risk for developing disseminated histoplasmosis.
17 similar role to play in the pathogenesis of histoplasmosis.
18 igen to protect mice in a model of pulmonary histoplasmosis.
19 n the lungs of C57BL/6 mice with reinfection histoplasmosis.
20 en these receptors for regulation reexposure histoplasmosis.
21 means of diagnosing the more severe forms of histoplasmosis.
22 he course of primary and secondary pulmonary histoplasmosis.
23 ferences in control of primary and secondary histoplasmosis.
24 with sera of healthy patients or those with histoplasmosis.
25 ntinued in 1 patient because of disseminated histoplasmosis.
26 of a protective immune response in pulmonary histoplasmosis.
27 opment of specific serodiagnostic assays for histoplasmosis.
28 se with different clinical manifestations of histoplasmosis.
29 s agent as a possible adjunctive therapy for histoplasmosis.
30 a frequently relied-on approach to diagnose histoplasmosis.
31 ion of the fungal diseases blastomycosis and histoplasmosis.
32 nt visit) and suspected (1 outpatient visit) histoplasmosis.
33 etween length of time on IMT and the risk of histoplasmosis.
34 for ocular inflammation but did not develop histoplasmosis.
35 x-matched control cohort who did not develop histoplasmosis.
36 ients died, and there were no recurrences of histoplasmosis.
37 herapy may develop pulmonary or disseminated histoplasmosis.
38 eeded for pneumocystosis, talaromycosis, and histoplasmosis.
39 imal method for diagnosis of acute pulmonary histoplasmosis.
40 e most sensitive and rapid means to diagnose histoplasmosis.
41 locker therapy after successful treatment of histoplasmosis.
42 a virulence in a murine model of respiratory histoplasmosis.
43 UAg) detection is an important biomarker for histoplasmosis.
44 r during lung infection in a murine model of histoplasmosis.
45 ility of Cfp4 as a diagnostic exoantigen for histoplasmosis.
46 after SOT is the period of highest risk for histoplasmosis.
47 series of patients undergoing treatment for histoplasmosis.
48 ere disease were risk factors for death from histoplasmosis.
49 the interplay between TNF-alpha and CCR5 in histoplasmosis.
50 reactions occurred in 96.3% of patients with histoplasmosis, 100% of patients with paracoccidioidomyc
51 cidioidomycosis (31.4%) and less common with histoplasmosis (14.0%) and blastomycosis (13.1%) versus
52 cidioidomycosis (31.4%) and less common with histoplasmosis (14.0%) and blastomycosis (13.1%) vs. inf
53 t reactivity with sera from 20 patients with histoplasmosis, 15 patients with blastomycosis, and 14 h
55 We immunologically characterized 10 cases of histoplasmosis, 4 of whom developed histoplasmosis IRIS.
56 ver was less common in blastomycosis (2.6%), histoplasmosis (5.3%) and coccidioidomycosis (9.4%) than
57 ver was less common in blastomycosis (2.6%), histoplasmosis (5.3%), and coccidioidomycosis (9.4%) tha
59 above the clinically relevant threshold for histoplasmosis, 69% (35/51) for coccidioidomycosis, and
64 ent, diagnosis, and outcomes associated with histoplasmosis after solid organ transplant (SOT), we re
65 onal study examining patients that developed histoplasmosis after the initiation of systemic immunomo
67 ed blastomycosis and one from a patient with histoplasmosis (also positive by the MiraVista Blastomyc
69 to provide the first prevalence estimates of histoplasmosis among individuals with advanced HIV in Co
70 the development of disseminated or pulmonary histoplasmosis among patients who are receiving systemic
71 des for symptoms or findings consistent with histoplasmosis and 35% had >=2 healthcare visits in the
74 amed after the etiologic agent, for example, histoplasmosis and aspergillosis, while this should not
75 efined as 100 cases/100 000 person-years for histoplasmosis and coccidioidomycosis and 50 cases/100 0
76 of serum from patients with acute pulmonary histoplasmosis and controls in the MVista Histoplasma an
77 specimens from patients with culture-proven histoplasmosis and controls were tested using both metho
78 neovascularization caused by presumed ocular histoplasmosis and demonstrated stabilization of the cho
79 rement can be useful for diagnosing systemic histoplasmosis and for monitoring treatment response, es
80 ing the initial host-pathogen interaction in histoplasmosis and have revealed an important mechanism
81 f participants with progressive disseminated histoplasmosis and respiratory symptoms had a positive B
82 choroidal neovascular membrane due to ocular histoplasmosis and to provide a treatment algorithm.
84 ns (cryptococcosis), Histoplasma capsulatum (histoplasmosis), and Talaromyces (Penicillium) marneffei
86 arget of the cellular immune response during histoplasmosis, and immunization with this protein is pr
87 diate protection in a murine model of lethal histoplasmosis, and it suggests a new candidate antigen
89 0 confers a salutary effect on the course of histoplasmosis, and the beneficial effects of IL-10 defi
91 3%) had any fungal-specific laboratory test: histoplasmosis antibody test (n = 349 [18%]), Histoplasm
92 is, and Histoplasma capsulatum, the agent of histoplasmosis, are known to form meiotic (sexual) stage
93 will likely be of benefit in presumed ocular histoplasmosis associated choroidal neovascularization.
96 histoplasmosis has a worldwide distribution, histoplasmosis-associated immune reconstitution inflamma
97 ed to describe the incidence and features of histoplasmosis-associated IRIS in a cohort of PLHIV.
100 detection in patients with culture-confirmed histoplasmosis at Mayo Clinic (Rochester, MN) over a 10-
101 equently developed pulmonary or disseminated histoplasmosis at the Mayo Clinic in Rochester, Minnesot
103 ide (25.0%) versus outside (28.7%) the U.S. "histoplasmosis belt." Aggregate sensitivity was 96.5% fo
106 strongyloidiasis, malaria, schistosomiasis, histoplasmosis, blastomycosis, and coccidioidomycosis.
107 tion against use of AmB+Flu for treatment of histoplasmosis, but studies of the effect of treatment o
108 ing regulates pathogen persistence in murine histoplasmosis by regulating Tregs exiting from the thym
112 We identified incident blastomycosis and histoplasmosis cases from 2013 to 2023 within Oracle EHR
115 cid sensor that can identify the presence of histoplasmosis causing fungal genes, in whole blood or b
117 The primary outcome was the incidence of histoplasmosis, coccidioidomycosis, and blastomycosis fo
120 nd from biopsy specimens from a patient with histoplasmosis contained fungal cells that were labeled
121 ed stored urine from patients diagnosed with histoplasmosis during an outbreak in Indianapolis which
122 and may indicate higher risk of disseminated histoplasmosis, especially in HIV infected patients.
123 pdate on findings concerning presumed ocular histoplasmosis etiology, epidemiology, and pathophysiolo
128 stating vision loss that may occur in ocular histoplasmosis from the development of an atrophic scar
129 mine if IFN-gamma is necessary in reexposure histoplasmosis, GKO and WT mice were inoculated with 10(
132 zoster virus (HR, 1.49 [95% CI, 1.18-1.89]), histoplasmosis (HR, 3.55 [95% CI, 1.10-11.42]), and Pneu
133 e limited data regarding the pathogenesis of histoplasmosis immune reconstitution inflammatory syndro
134 y with L-AmB versus control for disseminated histoplasmosis in AIDS, followed by oral itraconazole th
136 with acquired immunodeficiency syndrome and histoplasmosis in Brazil and United States were compared
141 fy all reports received through July 2001 of histoplasmosis in patients treated with either inflixima
142 modulates the protective immune response to histoplasmosis in SCID mice and also suggests that IL-12
144 Itraconazole is the preferred azole for histoplasmosis in the current Infectious Diseases Societ
147 te has one of the highest death rates due to histoplasmosis in the world, where the mortality rate va
148 es in 88.8% of patients with acute pulmonary histoplasmosis in this assay, while immunodiffusion, com
150 de a framework for the early pathogenesis of histoplasmosis in which yeast cell invasion of lung MPhi
151 ularization in patients with presumed ocular histoplasmosis, in particular that of subfoveal localiza
152 cases of opportunistic infection, including histoplasmosis, in patients treated with these products.
154 four significant adverse events: a suspected histoplasmosis infection; two Tenchkoff dialysis cathete
155 Research Databases to identify patients with histoplasmosis (International Classification of Diseases
173 gal meningitis, its role in the treatment of histoplasmosis is hampered by reduced activity and poten
177 nazole is increasingly used as treatment for histoplasmosis; it has in vitro activity against Histopl
178 nazole is increasingly used as treatment for histoplasmosis; it has in-vitro activity against Histopl
180 sent a rare case of primary gastrointestinal histoplasmosis manifesting with acute granulomatous hepa
181 illance suggests that acute life-threatening histoplasmosis may complicate immunotherapy with TNFalph
184 osis: Illinois, Kentucky, and West Virginia; histoplasmosis: Missouri, Iowa, and Oklahoma) that do no
186 ar manifestations of malaria, cysticercosis, histoplasmosis, mucormycosis, subacute sclerosing panenc
187 diasis (n = 10), cryptococcosis (n = 9), and histoplasmosis (n = 11) revealed three antigens with rel
188 s treated with infliximab, manifestations of histoplasmosis occurred within 1 week to 6 months after
190 ted histoplasmosis, primary gastrointestinal histoplasmosis of the liver in absence of lung involveme
191 on three patients who developed disseminated histoplasmosis on therapy with TNF-alpha inhibitors.
196 a valuable asset to support the diagnosis of histoplasmosis, particularly when direct detection metho
197 vestigate its potential for the follow-up of histoplasmosis patients during treatment, antigen titers
199 cognized by antibodies in 18 of 18 sera from histoplasmosis patients, but not by antibodies in sera f
201 elayed diagnosis of progressive disseminated histoplasmosis (PDH) results in high mortality rates.
202 -2017 for blastomycosis, coccidioidomycosis, histoplasmosis, pneumonia (viral, bacterial, Streptococc
203 -2017 for blastomycosis; coccidioidomycosis; histoplasmosis; pneumonia (viral, bacterial, Streptococc
204 Herein, we report a case of isolated CNS histoplasmosis presenting with pontine stroke and mening
205 liver involvement is common in disseminated histoplasmosis, primary gastrointestinal histoplasmosis
207 e the understanding of genetic influences on histoplasmosis, reveal how shifts in the composition of
210 c areas, screening for latent or subclinical histoplasmosis should be implemented before antiretrovir
211 Sera from four patients with disseminated histoplasmosis showed falls in antigen levels; three of
215 MD) (12), macular hole (10), presumed ocular histoplasmosis syndrome (6), proliferative diabetic reti
217 streaks, and idiopathy, and presumed ocular histoplasmosis syndrome is still under investigation.
218 roidal neovascularization in presumed ocular histoplasmosis syndrome or age-related macular degenerat
219 macular degeneration or the presumed ocular histoplasmosis syndrome or retinal neovascularization fr
223 al for patients with angioid streaks, ocular histoplasmosis syndrome, and idiopathic causes of choroi
225 n Histoplasma capsulatum and presumed ocular histoplasmosis syndrome, other reports document nearly i
226 ed debate on the etiology of presumed ocular histoplasmosis syndrome, there have been significant adv
227 shown to be associated with Presumed Ocular Histoplasmosis Syndrome-related choroidal neovasculariza
231 s), endemic fungal infections (mucormycosis, histoplasmosis, talaromycosis, sporotrichosis), and ende
232 insurance claims data to better characterize histoplasmosis testing and treatment practices and its b
233 usly shown in a murine model of disseminated histoplasmosis that IL-12, IFN-gamma, and TNF-alpha were
237 Assay performance as an aid for diagnosing histoplasmosis was assessed in a prospective cohort of 8
241 herapy while she was living in an area where histoplasmosis was endemic was thought to be the most li
242 terleukin (IL)-12 on the course of pulmonary histoplasmosis was examined in naive and immune mice.
244 was comparable to that of tuberculosis, and histoplasmosis was potentially responsible for preventab
250 vision loss in patients with presumed ocular histoplasmosis, well defined extrafoveal or juxtafoveal
252 individuals with culture- and antigen-proven histoplasmosis were evaluated using the LAMP assay.
254 presenting with different clinical forms of histoplasmosis were monitored at regular intervals for u
257 ated macular degeneration or presumed ocular histoplasmosis, whereas both alpha v beta 3 and alpha v
258 HPH mutant was avirulent in a mouse model of histoplasmosis, whereas the vma1/VMA1 strain was as path
259 to develop either disseminated or pulmonary histoplasmosis while receiving systemic immunosuppressiv
261 ublished cases of biopsy-proven disseminated histoplasmosis with cholestatic jaundice to highlight hi
262 rrently available laboratory diagnostics for histoplasmosis, with an emphasis on complexities of test
263 reasing incidence rates of blastomycosis and histoplasmosis, with increasing diagnoses outside of his
264 esented by PLHIV who presented an episode of histoplasmosis within 6 months after antiretroviral ther