コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 tages; 24 (38%) were diagnosed in primary or secondary syphilis.
2 e and seed new disseminated lesions to cause secondary syphilis.
3 for 70% or more of male cases of primary and secondary syphilis.
4 eral blood mononuclear cells from women with secondary syphilis.
5 ported cases of tuberculosis and primary and secondary syphilis.
6 d soles is a strong clue to the diagnosis of secondary syphilis.
7 tum, and 24/70 urine); in 62/73 clients with secondary syphilis (15/73 peripheral blood, 47/73 oropha
8 ding 8 (36.3%) of 22 persons with primary or secondary syphilis, 2 (20%) of 10 persons with early lat
10 Seventy clients had primary syphilis, 73 secondary syphilis, 86 early latent syphilis, 14 late la
11 luding 3 men with primary infections, 8 with secondary syphilis, 9 with early latent syphilis, 1 with
12 All immunoassays were 100% sensitive for secondary syphilis, 95.2%-100% sensitive for early laten
13 ulation, followed weeks later by the rash of secondary syphilis, a latent period, and in some cases,
14 tly different trends in rates of primary and secondary syphilis: Absolute increases in rates among bl
15 In adjusted models, JHR was associated with secondary syphilis (adjusted odds ratio [AOR], 2.91 [95%
16 f sex partners that describe how primary and secondary syphilis affects men who have sex with men (MS
17 oint, compared with 76%-89% of patients with secondary syphilis and 44%-79% with latent syphilis.
18 n and peripheral blood from 23 patients with secondary syphilis and 5 healthy control subjects recrui
19 detectable in blood and in the skin rash of secondary syphilis and persist in both compartments afte
20 agnosed: 26 (14%) primary syphilis, 54 (29%) secondary syphilis, and 111 (58%) early latent syphilis.
21 tage was 19% with primary syphilis, 47% with secondary syphilis, and 33% with early latent syphilis.
22 nal intercourse more commonly presented with secondary syphilis, and hence in whom the primary stage
23 77 (33%) had primary syphilis, 154 (66%) had secondary syphilis, and two (1%) had early latent syphil
24 thin 3-6 months after therapy for primary or secondary syphilis, and within 12-24 months for latent s
25 nal intercourse more commonly presented with secondary syphilis-and hence, had undetected syphilis du
26 in T. pallidum genomes of 3 individuals with secondary syphilis, associated with diminution of TprK d
28 ve analysis of MSM diagnosed with primary or secondary syphilis at Melbourne Sexual Health Centre bet
29 ve analysis of MSM diagnosed with primary or secondary syphilis at Melbourne Sexual Health Centre bet
30 treponemes to resolve lesions of primary and secondary syphilis, but cannot clear the treponemes that
31 course (AI) were more likely to present with secondary syphilis, compared to men who exclusively prac
32 intercourse were more likely to present with secondary syphilis, compared to MSM who did not practice
33 intercourse were more likely to present with secondary syphilis, compared to MSM who did not practise
37 diagnoses were repeatedly missed, including secondary syphilis, eczema herpeticum, gram-negative fol
38 ic infectious syphilis and relative falls in secondary syphilis for both HIV-positive and HIV-negativ
39 Although the annual incidence of primary and secondary syphilis has dropped to the lowest rate record
42 rend for increasing frequency of primary and secondary syphilis in developed countries, especially in
45 fails to detect a proportion of primary and secondary syphilis infections and may be insufficient in
47 e profiles of cells infiltrating primary and secondary syphilis lesions, reverse transcription and po
50 ntibodies exclusively against TprC(C), while secondary syphilis patients fail to mount a detectable a
51 EP clinic appointments or whether primary or secondary syphilis presented at unscheduled interval vis
53 cluding 135 clinically confirmed primary and secondary syphilis samples, the PCR-LwCas13a assay demon
56 ved JHR symptoms, which were associated with secondary syphilis stage, lack of HIV, and successful tr
58 d FTA-ABS were less sensitive in primary and secondary syphilis than TP-PA; TP-PA is the most specifi
60 ina who had lesions suggestive of primary or secondary syphilis were evaluated using molecular techni