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1 ete deficiency in the neutrophil response to oral candidiasis.
2 abrata are predominant fungi associated with oral candidiasis.
3 ed attenuated virulence in a murine model of oral candidiasis.
4 ather than IL-22 is vital in defense against oral candidiasis.
5 bited potent activity in two mouse models of oral candidiasis.
6 d have promise as therapeutic agents against oral candidiasis.
7 promise as therapeutic agents in humans with oral candidiasis.
8 naling hub mediating mucosal defense against oral candidiasis.
9 burning and dysgeusia are common symptoms of oral candidiasis.
10 f human innate immune response in preventing oral candidiasis.
18 ogues for dry mouth, topical antifungals for oral candidiasis, and topical corticosteroids for aphtho
20 n 11.5% (95% CI, 3.6% to 27%) higher risk of oral candidiasis, based on a meta-analysis of 6 observat
21 18% to 28%), placing individuals at risk of oral candidiasis, dental caries, dysgeusia, masticatory/
24 stic fungal pathogen that has been linked to oral candidiasis in AIDS patients, although it has recen
25 lbicans and that is commonly associated with oral candidiasis in human immunodeficiency virus-positiv
28 5-2.1; P jeroveci, IR, 1.3; 95% CI, 1.1-1.6; oral candidiasis, IR, 1.2; 95% CI, 1.0-1.5; cytomegalovi
31 ed findings from this study demonstrate that oral candidiasis may constitute a risk factor for dissem
32 and CXCL9 levels, and remission of alopecia, oral candidiasis, nail dystrophy, gastritis, enteritis,
33 ophil functions and which has been linked to oral candidiasis (OC), the most prevalent oral lesion in
36 next 12-18 months, and patients with either oral candidiasis or hairy leukoplakia and a low CD4:CD8
39 except for tuberculosis, and was largest for oral candidiasis, Pneumocystis pneumonia, and toxoplasmo
40 eveloped to investigate whether the onset of oral candidiasis predisposes the host to secondary staph
41 over 16 and 48 weeks but was associated with oral candidiasis (predominantly mild or moderate as reco
42 mab were upper respiratory tract infections, oral candidiasis (predominantly mild or moderate as reco
43 ults suggest that HIV-infected patients with oral candidiasis should be carefully monitored for subse
44 tease Sap6 is important for virulence during oral candidiasis since it degrades host tissues to relea
46 The findings demonstrated that in mice with oral candidiasis, subsequent exposure to S. aureus resul
48 Although DS is the most prevalent form of oral candidiasis, there are currently no feasible therap
49 ough IL-17, confers the dominant response to oral candidiasis through neutrophils and antimicrobial f
51 patients, summary risk was highest (>5%) for oral candidiasis, tuberculosis, herpes zoster, and bacte
52 species of yeast isolated from patients with oral candidiasis, which is frequently a symptom of human
53 f adverse effects (except for an increase in oral candidiasis with FSC and F) was similar among the t