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 Most patients (90%) were not neutropenic.
2 Four patients were neutropenic.
3 tients developed evidence of infection while neutropenic.
4 transcriptional repressor protein GFI-1 are neutropenic.
5 repressor oncoprotein Gfi1 are unexpectedly neutropenic.
6 PM was diagnosed, all patients but one were neutropenic.
7 We find no role in virulence, however, among neutropenic and corticosteroid-suppressed mice with DC r
12 (DC) induced by intravenous infection among neutropenic and nonimmunosuppressed mice, as well as in
15 e risk groups, the most vulnerable hosts are neutropenic and patients who are mechanically ventilated
16 t androgen receptor knockout (ARKO) mice are neutropenic and susceptible to acute bacterial infection
17 that gene-targeted Gfi-1-deficient mice are neutropenic and that Gfi-1 mutations cause human neutrop
18 dels were that the animals were not rendered neutropenic and they did not receive porcine mucin with
21 r syngeneic BMT, B6D2F(1) mice are no longer neutropenic, and by 3 wk, they demonstrate complete reco
22 d mice was decreased; however, mice were not neutropenic, and there was no difference in absolute blo
25 of lung dendritic cells was more immature in neutropenic animals than in nonneutropenic mice exposed
26 These findings coincided with the fact that neutropenic animals were more susceptible to A. hydrophi
30 e to greatly elevated lung TNF expression in neutropenic as compared with nonneutropenic animals.
33 inyl alcohol sponge wound model in mice made neutropenic by anti-Gr-1 Ab, as well as in cell culture.
36 Thromboembolism is frequent in hospitalized neutropenic cancer patients, including in perceived low-
38 litaxel, and carboplatin (lung infection and neutropenic colitis); two were considered to be related
39 he myeloid growth factors reduce the risk of neutropenic complications and may facilitate delivered d
40 myeloid growth factors to reduce the risk of neutropenic complications and sustain dose intensity con
42 nd cost of these agents in the prevention of neutropenic complications including febrile neutropenia.
45 bacterial concentration is very high, under neutropenic conditions or when there is neutrophil dysfu
46 Thus, targeting IL-4 might be beneficial in neutropenic conditions with increased susceptibility to
49 ichia mikurensis" infection in a chronically neutropenic dog from Germany was confirmed by DNA sequen
51 more age-dependent, associated with a modest neutropenic effect (9%, P = .012), demonstrated familial
52 t frequent causes of the abdominal pain were neutropenic enterocolitis (28%) and small bowel obstruct
54 to describe the population of patients with neutropenic enterocolitis admitted to an ICU and to inve
56 s of this entity that can help differentiate neutropenic enterocolitis from other gastrointestinal co
59 fungal disease reaches 20% in patients with neutropenic enterocolitis when enteritis is considered.
60 cally discussed in ICU patients admitted for neutropenic enterocolitis with radiologically assessed e
62 sis, leukemic meningitis, neutropenic fever, neutropenic enterocolitis, and transfussion-associated G
64 ient treatment is standard to manage febrile neutropenic episodes, although carefully selected patien
67 related to neutropenia present at baseline: neutropenic fever (13 of 25 subjects) and septic death (
68 (3.3% v 0.0%; P =.004), hospitalizations for neutropenic fever (13.4% v 1.5%; P <.001), hospitalizati
72 had serious adverse events, most frequently neutropenic fever (n=63, 38%), followed by pneumonia (n=
73 he most common grade 3-4 adverse events were neutropenic fever (seven patients [25%] in the 5-day gro
76 ohort, these infections were associated with neutropenic fever from an enteric source, and most isola
78 ppression was the major adverse effect, with neutropenic fever in 28 (23%) of 124 courses of therapy.
82 c: grade 3/4 neutropenia, four patients (one neutropenic fever); two patients had grade 3 thrombocyto
83 well tolerated with anticipated cytopenias, neutropenic fever, and disease-related fever, diarrhea,
84 herapy was well tolerated, with transfusion, neutropenic fever, and infection remaining the most freq
85 ient (4%) died from sepsis in the context of neutropenic fever, infection, and haemorrhage in the 5-d
86 -associated thrombosis, leukemic meningitis, neutropenic fever, neutropenic enterocolitis, and transf
87 with bleeding, grade 3 or 4 renal toxicity, neutropenic fever, or mucositis) was observed in 9.3% of
88 e 3 type 2 diabetes mellitus, mucositis, and neutropenic fever, were seen at the 2.2 mg/kg dose; ther
89 tment breaks were mediport complications and neutropenic fever, which occurred mostly at that dose le
95 adverse events that was most pronounced for neutropenic fever/infections and gastrointestinal events
98 transfusion of conditioned neutrophils in a neutropenic guinea pig model increased bacterial clearan
102 lera toxin was found to be protective to the neutropenic host, and this phenotype can be replicated b
104 the disease burden in immunocompromised and neutropenic hosts and causes serious congenital complica
105 ts, were found to accumulate in the lungs of neutropenic hosts challenged with killed or live-attenua
108 sis, a prototypic opportunistic infection in neutropenic hosts, is associated with marked accumulatio
109 negative patients, including pregnant women, neutropenic hosts, solid-organ or stem cell transplant r
115 ctable in mouse lungs, serum and BALF during neutropenic IA, suggesting that GT may be useful to diag
118 The SIGNIFICANT (Simple Investigation in Neutropenic Individuals of the Frequency of Infection af
119 s and elevated expression of ELA2 in vivo in neutropenic individuals that GFI1 represses ELA2, linkin
121 rcellular adhesion molecule (ICAM)-1-/-, and neutropenic-induced mice were subjected to 70% hepatecto
129 icant difference in toxicities was decreased neutropenic infections in patients treated with nelarabi
131 in source of early IFN-gamma in the lungs in neutropenic invasive aspergillosis, and this is an impor
134 Enrichment of GT in Aspergillus-infected neutropenic lung correlated with fungal burden and hypha
137 ony-stimulating factor increased survival of neutropenic mice after i.n. P. aeruginosa inoculation.
138 rmal mice but was outcompeted by MGAS2221 in neutropenic mice and had enhancements in expression of v
139 whereas the differences observed between the neutropenic mice and the saline-pretreated controls were
140 ion, myelin loss, and AQP4 loss in brains of neutropenic mice at 24 hours and 7 days, and increased s
141 e virulence defect was partially restored in neutropenic mice by adding gentamicin, an antibiotic tha
144 f granulocytes yielded 90% survivorship; all neutropenic mice died after the termination of treatment
149 An adoptive transfer of dendritic cells into neutropenic mice provided a protective effect during inv
153 n mutants in the lungs of wild-type (WT) and neutropenic mice using transposon sequencing (Tn-seq).
159 ciated with airway eosinophil recruitment in neutropenic mice with invasive pulmonary aspergillosis (
161 hen administered to diabetic ketoacidotic or neutropenic mice with mucormycosis, deferasirox signific
162 or only the first 24 h, or using genetically neutropenic mice), the cellular responses increased seve
164 mAb-induced tumor reduction, abolished in neutropenic mice, could be restored in FcgammaR-deficien
165 mutational analysis, we demonstrate that, in neutropenic mice, elimination of the A. nidulans pH-resp
168 accessory toxins in virulence is negated in neutropenic mice, which is consistent with a role of acc
169 in 51 genes still had significant defects in neutropenic mice, while mutants with insertions in 52 ge
186 s detected in 71% of sera and 50% of BALF of neutropenic mice; neither was detected in serum/BALF of
188 ltayaaA, and DeltaycgE mutants was higher in neutropenic mouse lungs, indicating that these genes enc
189 ced neutrophils (AINs) either in vitro or in neutropenic mouse model displayed strong bactericidal ac
190 enesis by A fumigatus both in vitro and in a neutropenic mouse model is mediated through secondary me
194 coccus pneumoniae septicemia mouse model and neutropenic mouse thigh infection model using methicilli
195 al experiments (n = 6, including 5 using the neutropenic mouse thigh infection model), and clinical s
199 ted combinations were further validated in a neutropenic murine pneumonia model, using human-like dos
200 dynamically linked variable in the S. aureus neutropenic murine pneumonia model; the fAUC/MIC ratio r
208 leukocytes; to produce disease in wild-type, neutropenic, or lysozyme-deficient rodents; and to induc
209 pment of fever and/or infections in afebrile neutropenic outpatients and recovery without complicatio
210 Secondary outcomes included: in afebrile neutropenic outpatients, infection-related mortality; in
212 ut when to begin empirical treatment after a neutropenic patient becomes febrile, whether and how to
213 gh-dose daptomycin (DAP) therapy failed in a neutropenic patient with bloodstream infection caused by
214 superiority trial, adult, febrile, high-risk neutropenic patients (FhrNPs) with hematologic malignanc
215 of A. fumigatus without developing disease, neutropenic patients and those receiving immunosuppressi
216 eages, and a partial response was defined in neutropenic patients as 100% increase in the absolute ne
217 ing of anti-gram-positive therapy to febrile neutropenic patients at risk of serious beta-lactam-resi
218 response to the invading fungi, not only in neutropenic patients but also in patients with normal or
221 Data from 569 unique cases of VGS BSI in neutropenic patients from 2000 to 2010 at the MD Anderso
222 miting empiric anti-gram-positive therapy to neutropenic patients having at least 1 of these 3 risk f
223 is efficacious and safe in low-risk febrile neutropenic patients identified with the help of the MAS
226 For example, the profound susceptibility of neutropenic patients to infection marks neutrophils (the
229 e compare two healthy individuals with seven neutropenic patients undergoing hematopoietic stem cell
232 and PCT levels were significantly higher in neutropenic patients with BSIs than in those without doc
233 idered the standard of treatment for febrile neutropenic patients with cancer, but this approach may
238 Granulocyte transfusions are beneficial in neutropenic patients with severe uncontrolled infection.
239 tions, especially among immunosuppressed and neutropenic patients, as well as a source of bacterial c
240 ntamination of platelets resulting in STR in neutropenic patients, failure of passive surveillance to
255 the risk of infection is greatest during the neutropenic period immediately following transplant, pat
256 G-CSF shortened the posttransplantation neutropenic period, but did not affect days +30 and +100
259 cultures in experiments using BAL fluid from neutropenic rabbits with experimentally induced IPA defi
264 tested in the murine listeriosis model, the neutropenic rat Pseudomonas aeruginosa infection, and th
267 g capability (decreased bacterial burden) in neutropenic recipient mice in both peritonitis and bacte
268 e effects for TH and TCH, respectively, were neutropenic-related complications, 29% and 23%; thromboc
271 n the phase 2 combination cohort (one due to neutropenic sepsis and one due to Escherichia coli sepsi
274 itabine plus cisplatin, but after two cycles neutropenic sepsis developed, which required a prolonged
275 tment-related deaths occurred; one caused by neutropenic sepsis in a patient with concurrent cytokine
280 amethasone group (one each of unknown cause, neutropenic sepsis, myocarditis, and Stevens-Johnson syn
289 nts was inhibited, without rendering animals neutropenic, suggesting an effect of G-CSF receptor bloc
290 of inflammatory cytokines, and when rendered neutropenic the mortality difference was abrogated.
292 o PK/PD comparison of 5x and PMB in a murine neutropenic thigh model against P. aeruginosa strains wi
294 th infectious risk, it permits assessment of neutropenic timepoints that were previously inaccessible
295 re quite common, whereas emergencies such as neutropenic typhlitis, pancreatitis, and acute haemolysi
300 staining was greater in cells isolated from neutropenic wounds than in those from control wounds.