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1 At admission, 25% (19/76) of children were afebrile.
2 e initially afebrile and 6 patients remained afebrile.
3 nd 16 (17%) and six (12%), if the patient is afebrile.
4 566 (34%) were febrile, and 1,125 (66%) were afebrile.
5 arum and 36 had P. vivax infections) and 162 afebrile adults (of whom 20 had P. falciparum and 20 had
12 her had neutropenic fever, and the third was afebrile and non-neutropenic at the time of presentation
14 ve therapy (80% v 53%); and (3) treatment of afebrile and uncomplicated febrile neutropenia (30% v 60
18 s and Treg cells using flow cytometry in 168 afebrile children (of whom 15 had P. falciparum and 36 h
20 om both virus-negative afebrile controls and afebrile children with the same viruses present in the f
21 ve febrile children from both virus-negative afebrile controls and afebrile children with the same vi
31 100 mg per kilogram per day until they were afebrile for 48 hours and 3 to 5 mg per kilogram per day
33 exclude febrile HCWs from working, but allow afebrile HCWs with respiratory symptoms to have contact
38 zation ranged between 79.1% and 88.0% in the afebrile malaria and hookworm groups with no significant
41 tion pre- and posttreatment in children with afebrile malaria, hookworm, and Schistosoma haematobium
42 v 4.6%); and (3) secondary prophylaxis after afebrile neutropenia following chemotherapy for germ cel
45 d: development of fever and/or infections in afebrile neutropenic outpatients and recovery without co
47 ividuals presented with febrile and multiple afebrile, often focal seizure types, multifocal epilepti
48 ulocyte colony-stimulating factor (G-CSF) in afebrile outpatients with severe chemotherapy-induced ne
53 gency department patients with septic shock, afebrile patients received lower rates of emergency depa
54 Routine therapeutic application of G-CSF in afebrile patients with severe neutropenia can reduce the
55 ge number of specimens from both febrile and afebrile patients, they were more prevalent in the plasm
56 time of high bacteremia that alternate with afebrile periods of relative well being during low bacte
61 emergency department IV fluids volume, being afebrile remained a significant predictor of in-hospital
67 illnesses are larger than those in normative afebrile subjects but smaller than dimensions in patient
68 nces in clinical characteristics (history of afebrile v febrile neutropenia), drug characteristics (G
69 They are the principal etiologic agents of afebrile viral upper-respiratory-tract infections (the c
70 ation required the patient with asthma to be afebrile with normal chest x-ray and white blood cell co
71 ive clusters, 59.7% were febrile, 20.2% were afebrile with other symptoms, and 20.2% were asymptomati
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