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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
8                      Efficacy is retained in neutropenic and corticosteroid-treated mice.
9 it(W/W-v) mice are MC-deficient, anemic, and neutropenic and have normal T cell compartments.
10                                      In both neutropenic and neutrophil-replete animals, the local re
11 terization revealed that these patients were neutropenic and NK cell deficient.
12  (DC) induced by intravenous infection among neutropenic and nonimmunosuppressed mice, as well as in
13 (levofloxacin) had 100% survivorship in both neutropenic and nonneutropenic groups.
14          There was no difference between the neutropenic and nonneutropenic patients in need of inten
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
19            Median age was 59 years; 19% were neutropenic, and 22% were in an intensive care unit on t
20                Among these, 88% (22/25) were neutropenic, and 76% (19/25) had leukemia.
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
23                                              Neutropenic animals and liver macrophage (Kupffer cell)
24                                 Infection of neutropenic animals resulted in increased levels of viru
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
27 mice with adhesion molecule deletions and in neutropenic animals.
28 he optimal exposures initially identified in neutropenic animals.
29 ork was undertaken in neutropenic versus non-neutropenic animals.
30 e to greatly elevated lung TNF expression in neutropenic as compared with nonneutropenic animals.
31 em cell transplantation and 640 (31.0%) were neutropenic at ICU admission.
32 seases, including infective endocarditis and neutropenic bacteremia.
33 inyl alcohol sponge wound model in mice made neutropenic by anti-Gr-1 Ab, as well as in cell culture.
34                            Abdominal pain in neutropenic cancer patients presents a unique clinical c
35                   This included 66,106 adult neutropenic cancer patients with 88,074 hospitalizations
36  Thromboembolism is frequent in hospitalized neutropenic cancer patients, including in perceived low-
37                                              Neutropenic colitis is characterized by right-sided colo
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
41                                              Neutropenic complications including febrile neutropenia
42 nd cost of these agents in the prevention of neutropenic complications including febrile neutropenia.
43 rade 3 to 4 toxicities were hematologic, few neutropenic complications resulted.
44 t variables that increase individual risk of neutropenic complications.
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
47               In patients treated in a PE, a neutropenic diet did not prevent major infection or deat
48                                            A neutropenic diet is often used to prevent infection in p
49 ichia mikurensis" infection in a chronically neutropenic dog from Germany was confirmed by DNA sequen
50                                Patients were neutropenic during a median of 14 days (9-22 d).
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
53                                              Neutropenic enterocolitis (NEC) is a life-threatening di
54  to describe the population of patients with neutropenic enterocolitis admitted to an ICU and to inve
55       Data from critically ill patients with neutropenic enterocolitis are scarce.
56 s of this entity that can help differentiate neutropenic enterocolitis from other gastrointestinal co
57                                              Neutropenic enterocolitis is a serious, potentially leth
58                                              Neutropenic enterocolitis occurs in about 5.3% of patien
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
61                                              Neutropenic enterocolitis, also referred to as typhlitis
62 sis, leukemic meningitis, neutropenic fever, neutropenic enterocolitis, and transfussion-associated G
63 , diagnosis, and management of patients with neutropenic enterocolitis.
64 ient treatment is standard to manage febrile neutropenic episodes, although carefully selected patien
65         Acute toxicities during TPE included neutropenic fever (10%) and during XPE, grade 3 or 4 ora
66 de >/=3 adverse events were pneumonia (20%), neutropenic fever (11%), and diarrhea (6%).
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
69 ), thrombocytopenia (12%), anemia (12%), and neutropenic fever (2%).
70 rade 3 hypersensitivity reaction (n = 1) and neutropenic fever (n = 1), both at 10 mg/kg.
71 common grade 3-4 adverse events overall were neutropenic fever (n=27) and pneumonia (n=18).
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
74  microg/kg did not reduce the probability of neutropenic fever after high-dose paclitaxel.
75                             The incidence of neutropenic fever after the first cycle of paclitaxel 25
76 ohort, these infections were associated with neutropenic fever from an enteric source, and most isola
77 ogic or electrolyte abnormalities, including neutropenic fever in 18%.
78 ppression was the major adverse effect, with neutropenic fever in 28 (23%) of 124 courses of therapy.
79                          Major infections or neutropenic fever occurred in 13% of patients.
80                                 There was no neutropenic fever or neutropenic sepsis.
81                                      All had neutropenic fever with symptoms of mucositis and/or ente
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
90                  There was only 1 episode of neutropenic fever.
91 ncluded one grade 4 diarrhea and one grade 4 neutropenic fever.
92 nd 3% of patients receiving TAP experiencing neutropenic fever.
93 ms commonly used in the empiric treatment of neutropenic fever.
94 3, n = 20 [33%]; grade 4, n = 2 [3%]) but no neutropenic fever.
95  adverse events that was most pronounced for neutropenic fever/infections and gastrointestinal events
96                                 Grade 3 or 4 neutropenic fevers (P=0.01), nausea and vomiting (P<0.00
97 es were observed in 10% of patients, with no neutropenic fevers or treatment-related death.
98  transfusion of conditioned neutrophils in a neutropenic guinea pig model increased bacterial clearan
99                               An established neutropenic guinea pig model of IPA caused by Aspergillu
100 llin/tazobactam alone in febrile, high-risk, neutropenic hematologic patients with cancer.
101  as crucial innate cellular effectors in the neutropenic host after active immunization.
102 lera toxin was found to be protective to the neutropenic host, and this phenotype can be replicated b
103 lethal bacterial infection in the profoundly neutropenic host.
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
106                       TRAIL-based therapy in neutropenic hosts may represent a novel antibacterial tr
107        The mechanism of this accumulation in neutropenic hosts was found to be augmented influx of DC
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
110  DC traffic and phenotype and is specific to neutropenic hosts.
111 or the treatment of refractory infections in neutropenic hosts.
112  strategy for the prevention of infection in neutropenic hosts.
113 minated candidiasis as once-daily therapy in neutropenic hosts.
114 g following low dose spore inhalation in non-neutropenic hosts.
115 ctable in mouse lungs, serum and BALF during neutropenic IA, suggesting that GT may be useful to diag
116 n alveolus bilayer model and in the lungs of neutropenic immunocompromised mice.
117                             However, not all neutropenic individuals develop infections, so the abili
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
120 cal management in well-appearing nonseverely neutropenic individuals.
121 rcellular adhesion molecule (ICAM)-1-/-, and neutropenic-induced mice were subjected to 70% hepatecto
122                               Mice were made neutropenic; infected or not with Staphylococcus aureus,
123 ged grade 4 neutropenia (n = 4), and grade 5 neutropenic infection (n = 1).
124  < .001), hand-foot syndrome (P < .001), and neutropenic infection (P < .001).
125 h 25 mg lenalidomide developed a grade 4 non-neutropenic infection and died.
126 ns controversial for patients at low risk of neutropenic infection.
127 rse events were leukopenia (eight [32%]) and neutropenic infections (five [20%]).
128  of 1.9% (64 of 3,402) was mainly related to neutropenic infections (n = 56; 87.5%).
129 icant difference in toxicities was decreased neutropenic infections in patients treated with nelarabi
130 pecific defense mechanisms in the context of neutropenic infections is limited.
131 in source of early IFN-gamma in the lungs in neutropenic invasive aspergillosis, and this is an impor
132                   Finally, in the context of neutropenic invasive aspergillosis, depletion of DCs res
133                 In the particular setting of neutropenic leukemia patients with pulmonary infection,
134     Enrichment of GT in Aspergillus-infected neutropenic lung correlated with fungal burden and hypha
135                               Interestingly, neutropenic lysozyme 2-diphtheria toxin A mice exhibited
136                 Anti-PMN-treated mice became neutropenic (mean, 349 cells/microL), experiencing an 84
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
142                                    Wounds in neutropenic mice contained 100-fold fewer neutrophils th
143                            Wound fluids from neutropenic mice contained 68% more TNF-alpha, 168% more
144 f granulocytes yielded 90% survivorship; all neutropenic mice died after the termination of treatment
145 48 mg/kg every 24 h in cohorts of normal and neutropenic mice for 5 days.
146                                           In neutropenic mice infected with wild-type A. fumigatus, i
147  alpha, suggesting the decreased survival in neutropenic mice is due to systemic shock.
148                            Most importantly, neutropenic mice lacking neutrophil-derived TRAIL were p
149 An adoptive transfer of dendritic cells into neutropenic mice provided a protective effect during inv
150         Because identical ischemic injury in neutropenic mice resulted in milder renal insufficiency
151                              At a high dose, neutropenic mice showed increased rates of survival comp
152                                          Non-neutropenic mice that were immunosuppressed with cortiso
153 n mutants in the lungs of wild-type (WT) and neutropenic mice using transposon sequencing (Tn-seq).
154           However, the bacterial load in the neutropenic mice was comparable to that of the saline-pr
155                   Simulation of this dose in neutropenic mice was highly effective in methicillin-sen
156 res of lung injury in wild-type mice whereas neutropenic mice were protected from such injury.
157               We found that, in the lungs of neutropenic mice with invasive aspergillosis, NK cells w
158 rked induction of MCP-1/CCL2 in the lungs of neutropenic mice with invasive aspergillosis.
159 ciated with airway eosinophil recruitment in neutropenic mice with invasive pulmonary aspergillosis (
160          ATAK cells improved the survival of neutropenic mice with lethal disseminated candidiasis an
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
163                                In uninfected neutropenic mice, ATAK cells spread from the mesentery i
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
166                                           In neutropenic mice, intranasal (i.n.) doses of P. aerugino
167                                           In neutropenic mice, the LPS-induced NF-kB activation and T
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
170 sponse in the skin and was fully virulent in neutropenic mice.
171 utrophil-depleting antibodies or genetically neutropenic mice.
172 sing ace2Delta Candida glabrata infection in neutropenic mice.
173  abscesses and decreased disease severity in neutropenic mice.
174  that effectively treat lethal infections in neutropenic mice.
175 , like wild-type bacteria, it was lethal for neutropenic mice.
176  Ag-specific T cells and DCs was improved in neutropenic mice.
177  protective during invasive aspergillosis in neutropenic mice.
178 corticosteroids, but had normal virulence in neutropenic mice.
179 % for normal mice and 80%, 100%, and 70% for neutropenic mice.
180 , during pulmonary invasive aspergillosis in neutropenic mice.
181 rimental invasive pulmonary aspergillosis in neutropenic mice.
182  antifungal response against A. fumigatus in neutropenic mice.
183 s disease (CGD), hydrocortisone-treated, and neutropenic mice.
184 fit in the lungs of WT mice than in those of neutropenic mice.
185  protective during invasive aspergillosis in neutropenic mice.
186 s detected in 71% of sera and 50% of BALF of neutropenic mice; neither was detected in serum/BALF of
187 increased in adiponectin-deficient mice in a neutropenic model of invasive aspergillosis.
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
191 ted and reduced pulmonary fungal burden in a neutropenic mouse model of invasive aspergillosis.
192                                         In a neutropenic mouse model of IPA, treatment with posaconaz
193                           Here, we show in a neutropenic mouse model that immunity induced by mucosal
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
196 active against MRSA than free mupirocin in a neutropenic murine lung infection model.
197  aspergillosis, we used a well-characterized neutropenic murine model.
198                              Subsequently, a neutropenic murine pneumonia model with simulated clinic
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
201                 In the Staphylococcus aureus neutropenic murine thigh-infection model, the ratio of t
202  constructed and found to be attenuated in a neutropenic, murine model of pulmonary infection.
203            Statistical analysis compared the neutropenic (n = 159) and nonneutropenic (n = 2421) pati
204 r WT thymocytes correct neutrophil counts in neutropenic nude mice.
205                        Athymic nude mice are neutropenic or have near-normal neutrophil counts, depen
206 ad attenuated virulence, unless animals were neutropenic or lysozyme deficient.
207 idence of death related to port infection in neutropenic or nonneutropenic populations.
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
211 mplications and overall mortality in febrile neutropenic outpatients.
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
219                                              Neutropenic patients continue to be at increased risk fo
220               Abdominal pain as a symptom in neutropenic patients continues to be a diagnostic and th
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
224                                      Febrile neutropenic patients should receive initial doses of emp
225 associated with more diverse taxa within the neutropenic patients than the healthy subjects.
226  For example, the profound susceptibility of neutropenic patients to infection marks neutrophils (the
227                         STR occurred only in neutropenic patients transfused with high bacterial load
228 al infections are accordingly encountered in neutropenic patients undergoing chemotherapy.
229 e compare two healthy individuals with seven neutropenic patients undergoing hematopoietic stem cell
230                                              Neutropenic patients were excluded.
231                                              Neutropenic patients were less likely to have a single p
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
234 oral combination therapy in low-risk febrile neutropenic patients with cancer.
235                                              Neutropenic patients with fever and abdominal symptoms (
236                              Furthermore, in neutropenic patients with lung injury, deterioration of
237                                           In neutropenic patients with severe sepsis or septic shock,
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
241 c infections in immunocompetent and severely neutropenic patients, respectively.
242                                           In neutropenic patients, we identified PRDM5 protein sequen
243 velopment of improved treatment regimens for neutropenic patients.
244 in the gastrointestinal tract, especially in neutropenic patients.
245 mbined remaining species to be isolated from neutropenic patients.
246 ause considerable morbidity and mortality in neutropenic patients.
247 s that causes life-threatening infections in neutropenic patients.
248  streptococcal endocarditis and infection in neutropenic patients.
249 e bacteria causing bloodstream infections in neutropenic patients.
250 ting that GT may be useful to diagnose IA in neutropenic patients.
251 n VGS causing bloodstream infection (BSI) in neutropenic patients.
252  of AFI, which was successfully treated in a neutropenic pediatric patient.
253 ssary antibiotic use in febrile, nonseverely neutropenic pediatric patients with cancer.
254      Prophylaxis was administered during the neutropenic period following each chemotherapy cycle.
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
257 g placebo for seven days during the expected neutropenic period.
258 f the cathelicidin gene, Cnlp, were rendered neutropenic prior to cutaneous infection.
259 cultures in experiments using BAL fluid from neutropenic rabbits with experimentally induced IPA defi
260 sive pulmonary aspergillosis in persistently neutropenic rabbits.
261 sive pulmonary aspergillosis in persistently neutropenic rabbits.
262  and protect against microbial invasion in a neutropenic rat model of gram-negative sepsis.
263                                       In the neutropenic rat model, daily administration of WAY-20219
264  tested in the murine listeriosis model, the neutropenic rat Pseudomonas aeruginosa infection, and th
265         When the proteins were injected into neutropenic rats, the group injected with PEG-GCSF showe
266 was not as efficient as PEG-GCSF in treating neutropenic rats.
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
269  XT was associated with higher GI, skin, and neutropenic-related toxicities.
270            Dose limiting toxicity comprising neutropenic sepsis (one patient) and grade 3 fatigue (on
271 n the phase 2 combination cohort (one due to neutropenic sepsis and one due to Escherichia coli sepsi
272 n the treatment of physician's choice group (neutropenic sepsis and septic shock).
273 y dosing scheme; 2 of these patients died of neutropenic sepsis complications.
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
276                  One elderly patient died of neutropenic sepsis in the first brentuximab-AVD cycle.
277                           One fatal event of neutropenic sepsis was reported in a patient allocated r
278 n the COMBO study, the MTD was 22 microg/kg (neutropenic sepsis).
279 b emtansine group [metabolic encephalopathy, neutropenic sepsis, and acute myeloid leukaemia]).
280 amethasone group (one each of unknown cause, neutropenic sepsis, myocarditis, and Stevens-Johnson syn
281                      One fatal toxic effect, neutropenic sepsis, occurred in the primary-chemotherapy
282                        One death, related to neutropenic sepsis, occurred on study.
283 were three treatment-related deaths owing to neutropenic sepsis.
284            There was no neutropenic fever or neutropenic sepsis.
285 CX group died of suspected treatment-related neutropenic sepsis.
286 ) robustly lowered the bacterial burden in a neutropenic Staphylococci murine infection model.
287 mpound 63 showed notable efficacy in a mouse neutropenic Staphylococcus aureus infection model.
288                                  The initial neutropenic state fostered an environment of increased d
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.
291 ioavailability and shows efficacy in a mouse neutropenic thigh infection model.
292 o PK/PD comparison of 5x and PMB in a murine neutropenic thigh model against P. aeruginosa strains wi
293         In vivo mouse systemic infection and neutropenic thigh model experimental results confirmed t
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
296                     GT levels were higher in neutropenic versus CGD or steroid-treated lungs.
297               Further work was undertaken in neutropenic versus non-neutropenic animals.
298  chest port removal in adults when placed in neutropenic versus nonneutropenic patient groups.
299                     MAGP2-deficient mice are neutropenic, which contrasts with monocytopenia describe
300  staining was greater in cells isolated from neutropenic wounds than in those from control wounds.

 
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