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1 psy/normal histology and high-grade squamous intraepithelial lesion.
2 sted case-control study of cervical squamous intraepithelial lesions.
3 ed in both low-grade and high-grade squamous intraepithelial lesions.
4 raepithelial lesions, or high-grade squamous intraepithelial lesions.
5 d risk of progression to high-grade squamous intraepithelial lesions.
6 40 participants (6%) had high-grade squamous intraepithelial lesions.
7 .61-1.20) for those with high-grade squamous intraepithelial lesions.
8 in a high proportion of high-grade squamous intraepithelial lesions.
9 women before and after treatment of cervical intraepithelial lesions.
10 ngly associated with detection of a squamous intraepithelial lesions 4-8 months earlier (odds ratio,
11 5 percent of all smears); low-grade squamous intraepithelial lesion, 44 (0.5 percent); high-grade squ
12 esion, 44 (0.5 percent); high-grade squamous intraepithelial lesion, 6 (0.1 percent); and squamous-ce
14 sible the simultaneous screening of cervical intraepithelial lesions and detection of C. trachomatis
16 lain the increased risk of cervical squamous intraepithelial lesions and invasive cervical cancer in
17 with the development of high-grade squamous intraepithelial lesions and invasive cervical cancer.
18 nificance (ASC-US) and patients negative for intraepithelial lesions and malignancy (NILM) (P </= 0.0
19 ad a higher frequency of advanced pancreatic intraepithelial lesions and more foci of invasive cancer
20 ed in SCCs compared with high-grade squamous intraepithelial lesions and normal squamous epithelia.
21 termined significance and low-grade squamous intraepithelial lesion) and CIN1+ was also significant.
22 e, and 17.0% had high- or low-grade squamous intraepithelial lesions) and were significantly associat
23 49 participants (24%) had low-grade squamous intraepithelial lesions, and 40 participants (6%) had hi
24 nfection (HPV), low- and high-grade squamous intraepithelial lesions, and cervical cancer stages I-IV
28 KPC) mice at 4 weeks of age (when pancreatic intraepithelial lesions are histologically evident).
29 val = 2.4-13.4) more likely to have squamous intraepithelial lesions associated with the detection of
30 d significance [ASCUS] or low-grade squamous intraepithelial lesions) because of an ASCUS Papanicolao
32 increased through ASCUS, low-grade squamous intraepithelial lesions, CIN1, and CIN2 (18%-25%), up to
35 ions with either CIN2 or high-grade squamous intraepithelial lesion cytology; cluster 3 included olde
37 rmal cervical tissues and low-grade squamous intraepithelial lesions from cervical cancers and most o
38 elial lesions and 1 of 12 low-grade squamous intraepithelial lesions had abnormal Fhit expression.
39 of primary normal cervix, low grade squamous intraepithelial lesions, high-grade squamous intraepithe
41 PV)-associated precancer high-grade squamous intraepithelial lesion (HSIL) in human immunodeficiency
42 e anal cancer precursor, high-grade squamous intraepithelial lesion (HSIL), frequently regresses spon
43 a higher burden of anal high-grade squamous intraepithelial lesions (HSIL) and anal cancer (AC) comp
44 ions (LSIL, n = 14), and high-grade squamous intraepithelial lesions (HSIL) grade 2 (CIN2, n = 8), an
45 t untreated, a subset of high-grade squamous intraepithelial lesions (HSIL) of the cervix will progre
46 lesions (LSIL), 21 with high-grade squamous intraepithelial lesions (HSIL), and 28 with invasive cer
47 lial neoplasia (CIN2-3), high-grade squamous intraepithelial lesions (HSIL), and invasive cervical ca
48 tances, women with ASC-H, low-grade squamous intraepithelial lesion, HSIL, and atypical glandular cel
49 low-grade and 1282 with high-grade squamous intraepithelial lesions (HSILs) diagnosed cytologically;
50 re than one third of the high-grade squamous intraepithelial lesions (HSILs) in screening populations
54 nvasive cervical cancer, high-grade squamous intraepithelial lesions (HSILs; n=166), or low-grade squ
56 rs and/or progression to high-grade squamous intraepithelial lesions (ie, cervical intraepithelial ne
59 AS mutations, and reliably detect pancreatic intraepithelial lesions in mice despite negative signals
60 cells, cannot exclude a high-grade squamous intraepithelial lesion, low-grade squamous intraepitheli
61 significance (ASCUS) and low-grade squamous intraepithelial lesion (LSIL) triage study (ALTS), who w
62 HPV test, and persistent low-grade squamous intraepithelial lesion (LSIL) were significantly associa
63 HIV-infected women with a low-grade squamous intraepithelial lesion (LSIL; benchmark indication for c
65 significance (ASC-US) or low-grade squamous intraepithelial lesions (LSIL) who were triaged with tes
66 significance (ASC-US) or low-grade squamous intraepithelial lesions (LSIL) who were triaged with tes
67 d 66 women diagnosed with low-grade squamous intraepithelial lesions (LSIL), 21 with high-grade squam
68 including normal cervix, low-grade squamous intraepithelial lesions (LSIL), high-grade SILs (HSIL),
69 amous cells (ASC, n = 5), low-grade squamous intraepithelial lesions (LSIL, n = 14), and high-grade s
71 ned significance (ASCUS), low-grade squamous intraepithelial lesions (LSILs), and high-grade SILs (HS
72 esions (HSILs; n=166), or low-grade squamous intraepithelial lesions (LSILs); were positive for human
73 ble analysis, a history of cervical squamous intraepithelial lesion (odds ratio [OR], 4.2; 95% confid
74 HPV16, HPV18, or both or low-grade squamous intraepithelial lesion or worse cytology had better sens
75 HPV16, HPV18, or both or high-grade squamous intraepithelial lesion or worse cytology had higher sens
77 s intraepithelial lesion, low-grade squamous intraepithelial lesions, or high-grade squamous intraepi
78 maging (BLI), we discovered that microscopic intraepithelial lesions precede the onset of peripheral
80 outcomes: high-risk HPV prevalence; squamous intraepithelial lesion (SIL) or cervical intraepithelial
81 cytologic evidence of a high-grade squamous intraepithelial lesion (SIL) were referred for colposcop
82 h MY09/MY11/HMB01 HPV primers), and squamous intraepithelial lesions (SIL) (by cytological examinatio
83 ions, abnormal cervical smears, and squamous intraepithelial lesions (SIL) among women with systemic
84 orted to be 1.2-83.3% for low-grade squamous intraepithelial lesions (SIL) and to be 13.3-83.3% for h
85 en human papillomavirus (HPV), anal squamous intraepithelial lesions (SIL), and human immunodeficienc
86 A (retinol) deficiency and cervical squamous intraepithelial lesions (SILs) in human immunodeficiency
88 ults, defined as at least low-grade squamous intraepithelial lesions (SILs), in 774 human immunodefic
89 are at increased risk for cervical squamous intraepithelial lesions (SILs), the precursors to invasi
93 ion have a higher risk for cervical squamous intraepithelial lesions than do women without HIV infect
94 e lesions progressed from low-grade squamous intraepithelial lesions to HSILs and finally to cancer.
95 of human papillomavirus-associated squamous intraepithelial lesions to invasive cervical cancer is p
96 preventing the progression of preneoplastic intraepithelial lesions to invasive pancreatic ductal ad
97 ancies in TRAMP mice progress from precursor intraepithelial lesions, to invasive carcinoma that meta
99 Undetermined Significance/Low-Grade Squamous Intraepithelial Lesion Triage Study (ALTS, 1997-2001), t
100 Undetermined Significance/Low-Grade Squamous Intraepithelial Lesion Triage Study provided blood sampl
101 termined Significance and Low-Grade Squamous Intraepithelial Lesion Triage Study who were treated for
102 undetermined significance-low-grade squamous intraepithelial lesion triage study with the use of unsu
103 termined Significance and Low-Grade Squamous Intraepithelial Lesion Triage Study, in which women were
105 Undetermined Significance/Low-Grade Squamous Intraepithelial Lesions Triage Study (ALTS), we determin
106 Undetermined Significance-Low-Grade Squamous Intraepithelial Lesion) Triage Study and who returned 1
107 n elevated risk for high-grade anal squamous intraepithelial lesions was associated with infection by
109 ease (ie, CIN 2 or 3, or high-grade squamous intraepithelial lesion) was 6.09 (3.87-9.60) compared wi
110 seases, compared with the risk of developing intraepithelial lesions, was not related to any of a lar
111 use by their partners, no cervical squamous intraepithelial lesions were detected in 32 patient-year
114 V-infected men with high-grade anal squamous intraepithelial lesions were significantly more likely t
115 on and progression rates of HPV and squamous intraepithelial lesions, were obtained from the literatu
116 in HPV-positive cervical high-grade squamous intraepithelial lesions when compared with normal cervic
117 termined significance and low-grade squamous intraepithelial lesions who are at higher and lower risk
118 untreated, some cervical high-grade squamous intraepithelial lesions will progress to invasive squamo
119 ng the pathological features of higher-grade intraepithelial lesions, yet did not exhibit chromosomal
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