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1 ic survival than mucinous adenocarcinoma and nonmucinous adenocarcinoma patients (log-rank, P < 0.001
2  approximately 5 mm; (c) lepidic predominant nonmucinous adenocarcinoma, representing histopathologic
3 mongst the 42 nodules of the 9 patients with nonmucinous adenocarcinoma, the mean tumor-to-background
4              HPV DNA was not detected in any nonmucinous adenocarcinomas including clear cell, serous
5                                              Nonmucinous but not mucinous tumors were significantly a
6 ding 54% (7/13) of mucinous and 63% (5/8) of nonmucinous carcinomas.
7 carcinomas, consisting of 17 mucinous and 11 nonmucinous carcinomas.
8 urate test for differentiating mucinous from nonmucinous cystic lesions.
9 urve (0.79) for differentiating mucinous vs. nonmucinous cystic lesions.
10 accuracy to distinguish between mucinous and nonmucinous cysts.
11  ability to distinguish between mucinous and nonmucinous cysts.
12 p15.1 is strongly associated with high grade nonmucinous epithelial ovarian cancer.
13 nocarcinoma that shows predominantly lepidic nonmucinous growth, which at CT is usually part solid bu
14  0.82-2.52) and 1.90 (95% CI: 0.95-3.80) for nonmucinous histology, respectively.
15 hich 1375 had mucinous histology and 860 had nonmucinous histology.
16 h pathologically proved mucinous (n = 9) and nonmucinous (n = 17) rectal tumors, MR imaging was perfo
17 % are mucinous and have worse prognoses than nonmucinous ones.
18 minimally deleted regions were identified in nonmucinous ovarian cancer.
19                                   Women with nonmucinous ovarian carcinoma (n = 1,001) enrolled onto
20 hould be offered to all women diagnosed with nonmucinous, ovarian carcinoma, regardless of family his
21 ant adenocarcinoma are now described, all as nonmucinous, predominantly invasive, may include a small
22                                 Mucinous and nonmucinous rectal tumors can be differentiated with MR
23 ugh overall CSS was similar for mucinous and nonmucinous subtypes, differences in stage distribution
24 tly higher in the mucinous compared with the nonmucinous tumors (P = .0004, P = .0008, and P = .00002
25 e odds ratio was 0.89 (95% CI 0.85-0.93) for nonmucinous tumors and 0.98 (95% CI 0.93-1.04) for mucin
26 (95% confidence interval (CI) 0.69-0.85) for nonmucinous tumors and 1.03 (95% CI 0.88-1.21) for mucin
27 ) was significantly and inversely related to nonmucinous tumors but not to mucinous tumors.
28 fference in odds ratios between mucinous and nonmucinous tumors).
29                                  The risk of nonmucinous tumors, but not mucinous tumors, was positiv
30                             Among women with nonmucinous tumors, increasing trends in risk of invasiv
31     Overexpression of PAFR was found in most nonmucinous types of ovarian cancer but not in HOSE and

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