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1 against EHEC O157:H7 using a murine model of gastrointestinal infection.
2 erance in a Caenorhabditis elegans model for gastrointestinal infection.
3 ll surface mucin, is an important barrier to gastrointestinal infection.
4 y response to limit invasive respiratory and gastrointestinal infection.
5 in addition to inlA appear to contribute to gastrointestinal infection.
6 uiring surgical management similar to direct gastrointestinal infection.
7 lmonella enterica serovar Typhimurium during gastrointestinal infections.
8 1917, a human probiotic strain used to treat gastrointestinal infections.
9 or their prophylactic or therapeutic role in gastrointestinal infections.
10 or the development of novel vaccines against gastrointestinal infections.
11 e to the development of new vaccines against gastrointestinal infections.
12 a nosocomial pathogen that can cause severe gastrointestinal infections.
13 otile bacterium, is a leading cause of human gastrointestinal infections.
14 eonates are considered highly susceptible to gastrointestinal infections.
15 prerequisite to protective immunity against gastrointestinal infections.
16 l therapeutic strategies in the treatment of gastrointestinal infections.
17 s), enteritis necroticans, and non-foodborne gastrointestinal infections.
18 sures to new pathogenic organisms that cause gastrointestinal infections.
19 rs (ABO, Lewis, and P) associated with other gastrointestinal infections.
21 er respiratory tract infections (171 [22%]), gastrointestinal infections (64 [8%]), eye, ear, nose, a
22 effect of vitamin A supplementation on viral gastrointestinal infections among young children living
23 To investigate in a cohort with previous gastrointestinal infection and a control group the preva
24 n of inlA is important for cell invasion and gastrointestinal infection and suggest that sigmaB-regul
25 -3 (5-HT3) antagonists, and the treatment of gastrointestinal infections and chronic abdominal pain.
26 a for the treatment of patients with chronic gastrointestinal infections and inflammatory bowel disea
27 All these patients are at similar risk of gastrointestinal infections, and the subsequent morbidit
29 is study, we report the human health risk of gastrointestinal infection associated with inhalation ex
30 ets may be beneficial in the defense against gastrointestinal infections, but their sustained activat
31 stressor exposure can have at the onset of a gastrointestinal infection by its ability to render a re
32 Ysa type III secretion (T3S) system enhances gastrointestinal infection by Yersinia enterocolitica bv
38 risk was higher among children who had had a gastrointestinal infection during the first year of life
41 produced in response to localized Salmonella gastrointestinal infection enable the pathogen to succes
42 es from children with severe respiratory and gastrointestinal infections has generated interest in un
43 d 2006-2007 regarding the development of any gastrointestinal infections, hospitalizations, and presc
45 introduction of surveillance of outbreaks of gastrointestinal infection in England and Wales in 1992.
46 r respiratory tract infection in addition to gastrointestinal infection in gnotobiotic pigs, confirmi
49 ost prevalent cause of antibiotic-associated gastrointestinal infections in health care facilities in
50 serovar Typhimurium (ST), a leading cause of gastrointestinal infections in humans, effects an overal
51 al presentation, diagnosis, and treatment of gastrointestinal infections in immunocompromised hosts i
53 particularly during the past year, regarding gastrointestinal infections in immunocompromised persons
54 orted by the dose-response relationship) and gastrointestinal infections in the first year of life ma
55 al presentation, diagnosis, and treatment of gastrointestinal infections in the immunocompromised hos
56 article reviews what is new in the field of gastrointestinal infections in the immunocompromised hos
57 he pathogenesis, diagnosis, and treatment of gastrointestinal infections in the immunocompromised hos
58 diagnostic and therapeutic skills regarding gastrointestinal infections in the immunocompromised hos
62 This technology can also be used to study gastrointestinal infections, inflammatory bowel disease,
63 sible for causing bronchitis, pneumonia, and gastrointestinal infections, is highly resistant to UV d
65 s in most hosts, then it is very likely that gastrointestinal infection occurs in humans as well.
67 show that following acute Toxoplasma gondii gastrointestinal infection of mice, control of commensal
70 levels of investment relative to burden for gastrointestinal infections ( pound254 million, 9.7%), s
72 pment of vaccines against the most important gastrointestinal infections remains a high priority.
75 cin is far less effective against chlamydial gastrointestinal infection than against genital infectio
80 es isolated from patients with uncomplicated gastrointestinal infection using DNA microarray analysis
81 genes with previously unproven phenotypes in gastrointestinal infection were tested in bovine ligated
85 by acute renal failure, usually occurs after gastrointestinal infection with Shiga toxin 2 (Stx2)-pro
87 although much less than that gained by prior gastrointestinal infection with the wild-type parent str
88 Campylobacter jejuni is a leading cause of gastrointestinal infections worldwide, due primarily to
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