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1 nfirmed chronic Trypanosoma cruzi infection (Chagas disease).
2 tion have been used to study heart damage in Chagas disease.
3 in these areas that aid in the management of Chagas disease.
4 Trypanosoma cruzi, the parasite that causes Chagas disease.
5 yme, can cure the acute and chronic forms of Chagas disease.
6 of Trypanosoma cruzi, the etiologic agent of Chagas disease.
7 ites in the hearts of those who succumbed to Chagas disease.
8 liant squaramides as candidates for treating Chagas disease.
9 te Trypanosoma cruzi, the causative agent of Chagas disease.
10 o capture the TcVac2-induced protection from Chagas disease.
11 Trypanosoma cruzi is the etiologic agent of Chagas disease.
12 the clinical and epidemiological aspects of Chagas disease.
13 factor to prevent myocardial damage in human Chagas disease.
14 ty on parasitemia in a murine model of acute Chagas disease.
15 Trypanosoma cruzi is the causative agent of Chagas disease.
16 vidence of its effectiveness against chronic Chagas disease.
17 nsible for human African trypanosomiasis and Chagas disease.
18 an Trypanosoma cruzi, the causative agent of Chagas disease.
19 ore attention and efforts towards control of Chagas disease.
20 an Trypanosoma cruzi, the causative agent of Chagas disease.
21 st Trypanosoma cruzi, the causative agent of Chagas disease.
22 logy in both the acute and chronic phases of Chagas disease.
23 rocycles can lead to useful cidal agents for Chagas disease.
24 an adjuvant therapy for treatment of chronic Chagas disease.
25 cellular parasite and the causative agent of Chagas disease.
26 e an important factor in the pathogenesis of Chagas disease.
27 merica and often leads to the development of Chagas disease.
28 leads for the development of drugs to treat Chagas disease.
29 pathomechanism of sustained inflammation in Chagas disease.
30 drugs to develop an efficient treatment for Chagas disease.
31 ction and oxidative stress may contribute to Chagas disease.
32 r efficacy studies in a mouse model of acute Chagas disease.
33 luding Trypanosoma cruzi, the agent of human Chagas disease.
34 4.4%) patients, 2 of them in early stages of Chagas disease.
35 and is efficacious in a mouse model of acute Chagas disease.
36 African sleeping sickness, leishmaniasis and Chagas disease.
37 tential to lead to new chemotherapeutics for Chagas disease.
38 onsible for prominent systemic congestion in Chagas disease.
39 tion, management, and etiologic treatment of Chagas disease.
40 of multinational control initiatives against Chagas disease.
41 refore an important target cell during acute Chagas disease.
42 kinetoplastid protozoan pathogen that causes Chagas disease.
43 e whole-blood transcriptome of patients with Chagas disease.
44 erminant in transmission and pathogenesis of Chagas disease.
45 om Trypanosoma cruzi, the causative agent of Chagas disease.
46 hen trying to understand the pathogenesis of Chagas disease.
47 f digestive pathologies of clinical forms of Chagas disease.
48 omen of childbearing age prevents congenital Chagas disease.
49 and CD1d by CD14(+) cells from patients with Chagas disease.
50 ac pathology in a BALB/c mouse model of live Chagas disease.
51 m of human African trypanosomiasis (HAT) and Chagas disease.
52 worse ventricular function in patients with Chagas disease.
53 Benznidazole is the drug of choice for Chagas disease.
54 Trypanosoma cruzi, the etiological agent of Chagas disease.
55 kg/day for 60 days in 30 adults with chronic Chagas disease.
56 ypanosomal activity in patients with chronic Chagas' disease.
57 nd more effective drugs for the treatment of Chagas' disease.
58 istry efforts to develop drug candidates for Chagas' disease.
59 dioprotective role during the acute stage of Chagas' disease.
60 an Trypanosoma cruzi, the causative agent of Chagas' disease.
61 utaneous infection in a mouse model of acute Chagas' disease.
62 e events in nervous tissues of patients with Chagas' disease.
63 Trypanosoma cruzi is the etiologic agent of Chagas' disease.
64 nctions and be important in the pathology of Chagas' disease.
65 present in the sera of patients with chronic Chagas' disease.
66 re released into the plasma of patients with Chagas' disease.
67 contribute to increased protein nitration in Chagas' disease.
68 stress may be important in the pathology of Chagas' disease.
69 odified proteins may be useful biomarkers of Chagas' disease.
70 st Trypanosoma cruzi, the causative agent of Chagas' disease.
71 tochondrial decay and oxidative pathology in Chagas' disease.
72 of mitochondrial functional decline in acute Chagas' disease.
73 of Trypanosoma cruzi, the causative agent of Chagas' disease.
74 ssion of parasite burden in a mouse model of Chagas' disease.
75 in Trypanosoma cruzi, the causative agent of Chagas' disease.
76 were uninfected control patients and 120 had Chagas disease (1 group had asymptomatic disease, and 2
77 atients with indeterminate/digestive form of Chagas disease (35.7%) compared with those with Chagas c
78 83%), 38 of 88 leishmaniasis (43%), 18 of 31 Chagas disease (58%), 7 of 28 SA blastomycosis (25%), an
79 0 million people in Latin America and causes Chagas disease, a chronic inflammatory disease with fata
80 cruzi parasites are the causative agents of Chagas disease, a leading infectious form of heart failu
82 rypanosoma cruzi is the etiological agent of Chagas disease, a neglected and emerging tropical diseas
84 zi is a protozoan parasite that causes human Chagas' disease, a leading source of congestive heart fa
85 Trypanosoma cruzi (the etiological agent of Chagas disease) adapting via trade-off among three diffe
87 suicide, liver cancer, diabetes, cirrhosis, Chagas disease, African trypanosomiasis, melanoma, and o
88 asite-derived protein, PDNF, produced by the Chagas' disease agent Trypanosoma cruzi, functionally mi
89 t patients diagnosed in the chronic phase of Chagas disease already exhibit heart involvement, and th
93 ct physiology, but also is a major vector of Chagas disease, an illness that affects approximately se
94 runcated into fragments that are specific to Chagas disease and have the potential to be used as diag
95 BIA platform for in situ diagnosis of human (Chagas disease and human brucellosis) and animal (bovine
96 osoma cruzi, which is the causative agent of Chagas disease and is a promising target for the develop
97 nt and severe manifestation of human chronic Chagas disease and is characterized by heart failure, ve
99 associated with activation of DN T cells in Chagas disease and that CD1d blocking leads to downregul
100 he role of adipocytes in the pathogenesis of Chagas disease and the associated metabolic alterations.
101 e indeterminate or cardiac clinical forms of Chagas disease and whether IL-17 expression can be corre
102 e associated with microthrombus formation in Chagas' disease and a known activator of iPLA2, increase
103 Trypanosoma brucei are parasites that cause Chagas' disease and African sleeping sickness, respectiv
105 Schistosomiasis, malaria, leishmaniasis, Chagas disease, and African sleeping sickness affect hun
107 Trypanosoma cruzi is the causative agent of Chagas disease, and infects 5-8 million people in Latin
109 kungunya, zika, yellow fever, leishmaniasis, chagas disease, and malaria, with highest incidences in
110 a cruzi ( T. cruzi ), the causative agent of Chagas disease, and the results of structure-activity in
111 al diseases (11 with schistosomiasis, 5 with Chagas' disease, and 10 with cutaneous leishmaniasis), a
112 t in vivo behavior during the acute phase of Chagas disease; and (iii) neither nonspecific toxicity n
113 peutic strategies for the treatment of acute Chagas disease are feasible and that this approach may w
117 evidenced by recent microepidemics of acute Chagas disease attributed to the consumption of parasite
118 Trypanosoma cruzi, the etiological agent of Chagas disease, bears primary responsibility for produci
120 on, AhR influences the development of murine Chagas disease by modulating ROS production and regulati
122 e to another, and present case estimates for Chagas disease came from various sources, including WHO
123 e events described in human and experimental Chagas disease can contribute to, or aggravate, this pat
124 Chagas disease occur annually due to chronic Chagas disease cardiomyopathy (CCC), an inflammatory car
137 Cardiomyopathy is a serious complication of Chagas' disease, caused by the protozoan parasite Trypan
140 IC50 at 11.9 and 17.2 muM against neglected Chagas' disease causing Trypanosoma cruzi, respectively.
141 age with benznidazole to prevent congenital Chagas disease (CCD), as well as the usefulness of polym
143 of only 2 medications available for treating Chagas disease (CD) and currently the only drug availabl
145 rs for Disease Control and Prevention (CDC), Chagas disease (CD) may affect 1.31% of Latin American i
147 e findings suggest that during the course of Chagas disease, CD8(+) T cells undergo a gradual loss of
153 Trypanosoma cruzi, the causative agent of Chagas disease, contains exclusively iron-dependent supe
155 icular (human African trypanosomiasis (HAT), Chagas disease, cutaneous leishmaniasis, and malaria) ha
156 in toxicity of benznidazole in patients with Chagas disease, determine the serum cytokine profile, an
157 se and conclude with a view of the future of Chagas disease diagnosis, pathogenesis, therapy, and pre
159 Trypanosoma cruzi, the causative agent of Chagas disease, encodes for an alpha-carbonic anhydrase
160 etiologic agent of American trypanosomiasis (Chagas disease), exhibiting IC(50) values in the nanomol
161 man parasite Trypanosoma cruzi, the agent of Chagas' disease, expresses a membrane-bound neuraminidas
162 in the pathogenesis of experimental chronic Chagas disease, favoring inflammation and fibrogenesis.
167 n the USA (Lyme disease $2.5 billion), where Chagas disease has not been traditionally endemic, sugge
169 by Trypanosoma cruzi, the causative agent of Chagas disease, has recently been described, with differ
170 cardiomyopathy, the main clinical problem in Chagas' disease, has been extensively studied but is sti
173 of Trypanosoma cruzi, the etiologic agent of Chagas disease, have been highly inefficient, and no end
174 ected Trypanosoma cruzi, the causal agent of Chagas disease, implying the existence of evasion or tol
175 substantially ameliorates symptoms of acute Chagas disease in a mouse model with no apparent toxicit
178 ritic cell-based immunotherapeutic for acute Chagas disease in an attempt to delay or prevent the car
181 e have been major advances in the control of Chagas disease in most of the countries endemic for this
182 s as means of identifying new drugs to treat Chagas disease in the acute phase with greater activity,
183 , there are approximately 8 million cases of Chagas disease in the southern cone of South America alo
185 the blood of various tetrapods and vector of Chagas' disease in humans, carries in its genome four di
188 zi, the protozoan parasite that causes human Chagas' disease, induces a type I interferon (IFN) (IFN-
193 revent the deadly cardiac pathology in human Chagas disease is a desirable and currently unattained g
207 nd mortality in areas of Latin America where Chagas disease is endemic and among infected individuals
214 oximately 8 million people in Latin America, Chagas disease is now becoming a serious global health p
222 Trypanosoma cruzi infection (which causes Chagas disease) is typically undiagnosed and persists if
223 Trypanosoma cruzi, the etiological agent of Chagas disease, is a protozoan parasite with a complex l
224 infection, which is the etiological agent of Chagas disease, is associated with intense inflammation
225 fection, schistosomiasis, leishmaniasis, and Chagas disease, is being led by nonprofit product develo
226 Trypanosoma cruzi, a parasite that causes Chagas' disease, is endemic in parts of Mexico, South Am
227 olvement of MBL/MASP2-associated pathways in Chagas' disease, it is currently unknown whether MBL pla
228 Trypanosoma cruzi, the causing agent of Chagas disease, leads to an activation of the immune sys
229 s against other protozoal species: T. cruzi (Chagas disease), Leishmania major (cutaneous leishmanias
231 ive agents of human African trypanosomiasis, Chagas disease, leishmaniasis, and malaria, respectively
232 ding malaria, human African trypanosomiasis, Chagas disease, leishmaniasis, filariasis, and schistoso
233 in eastern Burma and vector-borne diseases (Chagas' disease, leishmaniasis, and yellow fever) in Col
234 Whether asymptomatic individuals at risk of Chagas disease living in Europe should be screened and t
235 against cruzain, a thiol protease target for Chagas disease, looking for reversible, competitive inhi
236 with at least three different techniques for Chagas disease, maintained at controlled low temperature
238 Trypanosoma cruzi, the protozoan that causes Chagas' disease, modulates the extracellular matrix netw
239 gest that galectin-3 is strongly involved in Chagas disease, not only in the immune response against
240 Approximately 12000 deaths attributable to Chagas disease occur annually due to chronic Chagas dise
241 OS] in the Treatment of Asymptomatic Chronic Chagas Disease [P05267] [STOP CHAGAS]: NCT01377480).
242 d neurotrophic factor (PDNF) produced by the Chagas' disease parasite Trypanosoma cruzi binds nerve g
246 verall, this work provides new insights into Chagas disease pathogenesis and presents an analytical c
247 >100 years ago, much has been learned about Chagas disease pathogenesis; however, the outcome of T.
248 Prospective observational study where adult Chagas disease patients accepting to receive benznidazol
253 ls with chronic indeterminate (asymptomatic) Chagas' disease potently blocked invasion of Trk-bearing
259 ted therapeutic options to prevent and treat Chagas disease put 8 million people infected with T. cru
260 mended for all cases of acute and congenital Chagas disease, reactivated infection, and chronic T cru
261 role of autoimmunity in the pathogenesis of Chagas disease remain unanswered, the development of aut
264 Trypanosoma cruzi, the etiologic agent of Chagas disease, resists extreme fluctuations in osmolari
265 panosomes are causative agents of Nagana and Chagas disease respectively, and speciated about 300 mil
267 investigated include malaria, leishmaniasis, Chagas' disease, roundworm, whipworm, pinworm, Chinese l
269 rformed an economic evaluation of systematic Chagas disease screening of the Latin American populatio
271 A potential drug target for treatment of Chagas disease, sterol 14alpha-demethylase from Trypanos
272 since the 1990s, but symptomatic congenital Chagas disease still represents a significant, albeit ch
273 iomyocytes, as well as in the mouse model of Chagas disease, supporting the involvement of TcAPx-CcP
274 eir partnership in the immunopathogenesis of Chagas disease, the chronic infection caused by the intr
275 Trypanosoma cruzi, the parasite that causes Chagas disease, the elongated, flagellated trypomastigot
276 azole are the front-line drugs used to treat Chagas disease, the most important parasitic infection i
277 te the possibility of using RDTs to diagnose Chagas disease, thereby decreasing the time to treatment
278 or Trypanosoma cruzi, the causative agent of Chagas' disease, to escape from the host immune system a
279 a cruzi parasite is the etiological agent of Chagas disease, treatment is still plagued by limited ef
280 ganisms, including the etiological agents of Chagas disease (Trypanosoma cruzi) and African sleeping
281 date tipifarnib kills the causative agent of Chagas disease, Trypanosoma cruzi, by blocking ergostero
282 of genomic DNA from the parasite that causes Chagas disease, Trypanosoma cruzi, directly in whole, un
283 e: Trypanosoma cruzi, the causative agent of Chagas disease; Trypanosoma brucei, the causative agent
285 o cross-sectional data of infestation by the Chagas disease vector Triatoma infestans in the city of
289 that the sylvatic (animal-infected) cycle of Chagas' disease was probably well established at the tim
290 with Rhodnius prolixus, the insect vector of Chagas disease, we show that an ovary dual oxidase (Duox
292 ne bug Rhodnius prolixus is a main vector of Chagas disease, which affects several million people, mo
295 study included 158 individuals with chronic Chagas disease who underwent cardiac magnetic resonance.
296 an heart samples obtained from subjects with Chagas disease who underwent heart transplantation showe
297 cellular experiments, cures the experimental Chagas disease with 100% efficacy, and suppresses viscer
298 HF) with reduced ejection fraction caused by Chagas' disease, with other etiologies, in the era of mo
299 ical aspects of the disease, such as chronic Chagas disease without detectable cardiac pathology, as
300 soma cruzi leads to the development of human Chagas' disease, yet the functional contributions of the
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