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1 ptibility and improve infectious outcomes in neonatal sepsis.
2 hey are a potential protective agent against neonatal sepsis.
3 e predominantly associated with detection of neonatal sepsis.
4 iotic classes, including those used to treat neonatal sepsis.
5 cribed antibiotics used for the treatment of neonatal sepsis.
6 n is crucial to prevent antibiotic-resistant neonatal sepsis.
7 preventable and among these, 10% are due to neonatal sepsis.
8 agnostic, and prognostic clinical utility in neonatal sepsis.
9 neonates who died from perinatal asphyxia or neonatal sepsis.
10 multiple antibiotic-resistant lineages cause neonatal sepsis.
11 s with very low birth weight from late-onset neonatal sepsis.
12 second-line empiric antibiotic regimens for neonatal sepsis.
13 quisition of S. agalactiae, a major cause of neonatal sepsis.
14 gesting an impaired bactericidal response in neonatal sepsis.
15 mly selected 422 of which 12.8% (n = 54) had neonatal sepsis.
16 ising avenues to prevent and/or treat severe neonatal sepsis.
17 acterial interactions in the early stages of neonatal sepsis.
18 inolyticus may be an underdiagnosed cause of neonatal sepsis.
19 f death and had either perinatal asphyxia or neonatal sepsis.
20 eterm infants are at high risk of developing neonatal sepsis.
21 nts to prevent necrotizing enterocolitis and neonatal sepsis.
22 perbilirubinemia, neonatal hypoglycemia, and neonatal sepsis.
23 ological processes undergo disruption during neonatal sepsis.
24 are non-specific and could be confused with Neonatal sepsis.
25 ciated with the inclusion of only EOS or all neonatal sepsis.
26 ogens when determining antibiotic choice for neonatal sepsis.
27 nes and their relatedness to strains causing neonatal sepsis.
28 owth of pathogens frequently associated with neonatal sepsis.
29 ing efforts designed to reduce the burden of neonatal sepsis.
30 e agent influence the clinical expression of neonatal sepsis.
31 tiae (GBS) is the leading cause worldwide of neonatal sepsis.
32 neumoniae, two pathogens commonly related to neonatal sepsis.
33 specially in the setting of culture-negative neonatal sepsis.
34 nces in the incidence of chorioamnionitis or neonatal sepsis.
35 ality and its mechanism in a murine model of neonatal sepsis.
36 r immune-modulating adjunctive therapies for neonatal sepsis.
37 The primary outcome was the incidence of neonatal sepsis.
38 coccus, the leading pathogens of early-onset neonatal sepsis.
39 neonates can be used to augment survival to neonatal sepsis.
40 is known about the role of MyD88 or TRIF in neonatal sepsis.
41 often shares similar clinical features with neonatal sepsis.
42 c, prognostic and therapeutic strategies for neonatal sepsis.
43 vent a significant proportion of early-onset neonatal sepsis.
44 of their potential to impact mortality from neonatal sepsis.
45 cent literature on novel diagnostic tests in neonatal sepsis.
46 a critical role for CXCL10 signaling during neonatal sepsis.
47 the association between HMOs and late-onset neonatal sepsis.
48 the incidence and mortality associated with neonatal sepsis.
49 noglobulin and colony-stimulating factors in neonatal sepsis.
50 itis and delivered neonates with early-onset neonatal sepsis.
51 sues, and reduced body weight and death from neonatal sepsis.
52 ly reduce both the incidence and severity of neonatal sepsis.
53 s pneumoniae is a rarely recognized cause of neonatal sepsis.
54 r ankle, two had Blount disease, and one had neonatal sepsis.
55 ty contributes to increased mortality during neonatal sepsis.
56 0.8%; RD, 0.04 [95% CI, -0.27 to 0.35]) and neonatal sepsis (1.3% vs 1.3%; RD, 0.02 [95% CI, -0.38 t
58 t preterm birth complication, 128 (45%) with neonatal sepsis, 69 (24%) with lower respiratory infecti
61 find prevalence and factors associated with neonatal sepsis among neonates admitted in Kibungo Refer
63 etermine the incidence and associations with neonatal sepsis and all-cause mortality in facility-born
65 tant (AMR) healthcare-associated infections, neonatal sepsis and community-acquired liver abscess, an
68 val rates from serious infections, including neonatal sepsis and health-care-associated infections, a
69 eading pathogen globally underlying cases of neonatal sepsis and is frequently resistant to antibioti
70 lebsiella pneumoniae is the leading cause of neonatal sepsis and is increasingly difficult to treat o
71 Nevertheless, limited information exists on neonatal sepsis and its associated factors in Rwanda.
72 hydrocephalus with and without a history of neonatal sepsis and meningitis (hydrocephalus cohort) fr
73 B Streptococcus (GBS) is a leading cause of neonatal sepsis and meningitis and an important cause of
74 richia coli K1 is the leading cause of human neonatal sepsis and meningitis and is important in other
75 Streptococcus (GBS) is the leading cause of neonatal sepsis and meningitis in developed countries.
76 Streptococcus (GBS) is the foremost cause of neonatal sepsis and meningitis in the United States.
79 oup B streptococci (GBS), a leading cause of neonatal sepsis and meningitis, are transferred to neona
80 B Streptococcus [GBS]) is a leading cause of neonatal sepsis and meningitis, peripartum infections in
81 Key features of Escherichia coli K1-mediated neonatal sepsis and meningitis, such as a strong age dep
88 New interventions are needed to decrease neonatal sepsis and mortality in regions with highest bu
90 ed coverage of antibiotics for pneumonia and neonatal sepsis and of oral rehydration solution for dia
91 used to investigate factors associated with neonatal sepsis and parametric survival models for facto
92 is 89% and 83% for cut-offs of 10ng/mL (for neonatal sepsis and pelvic inflammatory disease) and 30n
93 ination on cases and deaths of K. pneumoniae neonatal sepsis and project the global effects of routin
94 ognized effector of IL-18-mediated injury in neonatal sepsis and that disruption of the deleterious a
95 model, we used data from 3 global studies of neonatal sepsis and/or mortality-with 2,330 neonates who
96 dhood illnesses (eg, pneumonia, malaria, and neonatal sepsis) and delivery of preventive intervention
97 om perinatal asphyxia, 562 (47.0%) died from neonatal sepsis, and 156 (13.1%) from both conditions.
99 bstantial proportion of neonates who develop neonatal sepsis, and the high mortality rates among neon
103 is one of the most common organisms causing neonatal sepsis as well as serious infections in adults.
105 and South Asia, with perinatal asphyxia and neonatal sepsis being the leading causes of neonatal mor
107 oxygen therapy, the presence of concomitant neonatal sepsis, BPD, IVH, PDA, and NEC further increase
109 or to chorioamnionitis, fetal infection, and neonatal sepsis, but the understanding of specific facto
110 tes an inflammatory cytokine response during neonatal sepsis by directly compromising control of bact
112 deaths and 399,015 [CrI: 334,523 to 485,442] neonatal sepsis cases yearly worldwide, accounting for m
117 siders country-level trends in K. pneumoniae neonatal sepsis deaths and is unable to consider within-
118 n credible interval (CrI): 5.24 to 41.42] of neonatal sepsis deaths are caused by meropenem-resistant
120 neonates who died from perinatal asphyxia or neonatal sepsis determined by postmortem diagnostics.
125 ints, transcriptional interrogation of human neonatal sepsis finds upregulation of many genes involve
126 se and burden of antimicrobial resistance in neonatal sepsis for seven LMICs in Africa and South Asia
131 antibiotic combinations for the treatment of neonatal sepsis in areas with high rates of multidrug-re
133 findings suggest that a large proportion of neonatal sepsis in developing countries could be effecti
134 reptococcus (GBS) remains a leading cause of neonatal sepsis in high-income contexts, despite decline
137 negative bacteria (GNB) are a major cause of neonatal sepsis in low- and middle-income countries (LMI
138 ion could reduce the burden of K. pneumoniae neonatal sepsis in low- and middle-income countries (LMI
139 egative (GN) pathogens are a common cause of neonatal sepsis in low- and middle-income countries.
140 is found to be identical to isolates causing neonatal sepsis in Pakistan over similar time periods.
141 fatality, and underlying comorbidities, and neonatal sepsis incidence and case fatality within the n
142 w of technologies for the rapid diagnosis of neonatal sepsis includes new adaptations of time-honored
143 to identify major biomarkers associated with neonatal sepsis including Serum Amyloid A (SAA), C - rea
144 Considering the fact that the incidence of neonatal sepsis increases dramatically with decreasing g
149 omes (perinatal death, chronic lung disease, neonatal sepsis, intraventricular hemorrhage >grade 2, p
155 tment with a Toll-like receptor 4 agonist to neonatal sepsis is dependent on an endogenous CXCL10 res
156 re efficient and effective identification of neonatal sepsis is needed to target interventions to red
162 ility and clinical data for 916 out of 1,038 neonatal sepsis isolates (97 isolates were not recovered
163 antial progress has been achieved concerning neonatal sepsis, its lethality remains considerably high
164 de range of other acute illnesses, including neonatal sepsis-like disease, acute flaccid paralysis, a
166 up B Streptococcus (GBS) is a major cause of neonatal sepsis, meningitis in early infancy, postpartum
167 e whether Paenibacillus spp is a pathogen in neonatal sepsis, meningitis, and postinfectious hydrocep
170 n in neonatal respiratory distress syndrome, neonatal sepsis, necrotising enterocolitis, and admissio
173 e 17.7% of very low birth weight infants had neonatal sepsis, only 2.1% of low birth weight and 0.6%
175 er, S. bovis is capable of causing fulminant neonatal sepsis or meningitis that is indistinguishable
180 bor, intraamniotic or postpartum infections, neonatal sepsis, or admission of the infant to the neona
181 ect C-reactive protein (CRP)-a biomarker for neonatal sepsis, pelvic inflammatory disease, and inflam
182 es of 150 neonates with possible early-onset neonatal sepsis (pEOS) were obtained at the Hopital Prov
183 most significant bacterial pathogen causing neonatal sepsis, pneumonia and meningitis in the USA des
184 most significant bacterial pathogen causing neonatal sepsis, pneumonia, and meningitis in the United
186 n might be a crucial tolerance mechanism for neonatal sepsis preserving neural control of breathing.
189 ectrum antibiotics for suspected early-onset neonatal sepsis (sEONS) may have pronounced effects on g
190 lk samples from the mother of an infant with neonatal sepsis; sequencing of the enterovirus isolate i
191 l as other extracellular bacterial agents of neonatal sepsis (staphylococci and enterococci) induced
193 lop a severity score predicting mortality in neonatal sepsis to inform future clinical trial design.
194 common causes such as maternal hypertension, neonatal sepsis, twin-twin transfusion, alloimmunization
196 In this nationwide cohort study, early-onset neonatal sepsis was associated with an approximately 2-f
200 an the normative mean, and for children with neonatal sepsis were 0.73 SD lower on average than the n
201 use in lower respiratory tract infection and neonatal sepsis were observed between WHO regions and co
202 entified HLA-DRhiCD83+ gammadelta T cells in neonatal sepsis, which expressed genes related to antige
204 ms were the predominant cause of early-onset neonatal sepsis, with a high prevalence of extended-spec
205 a pneumoniae (n = 258) was the main cause of neonatal sepsis, with Serratia marcescens (n = 151), Kle