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1 reduced risk of breast cancer among pre- and postmenopausal women.
2 e vulnerabilities for ER(+) breast cancer in postmenopausal women.
3 trogen action and frequently occurs in older postmenopausal women.
4 C-reactive protein in both premenopausal and postmenopausal women.
5 have high rates of recurrence, especially in postmenopausal women.
6 is promising for preexposure prophylaxis in postmenopausal women.
7 ted with worsened breast cancer prognosis in postmenopausal women.
8 but not consistently in oestrogen-deficient postmenopausal women.
9 f hormone receptor-positive breast cancer in postmenopausal women.
10 vels of parathyroid hormone (PTH) in healthy postmenopausal women.
11 isk of death as a result of breast cancer in postmenopausal women.
12 primary preventive measures for, insomnia in postmenopausal women.
13 itable for application in this population of postmenopausal women.
14 sociations of ESH and T2D were based only in postmenopausal women.
15 increases the risk of endometrial cancer in postmenopausal women.
16 ial effect on bone turnover markers (BTM) in postmenopausal women.
17 primary prevention of chronic conditions in postmenopausal women.
18 eased risk of incident HF hospitalization in postmenopausal women.
19 eased breast cancer incidence in a cohort of postmenopausal women.
20 tive as a screening tool for osteoporosis in postmenopausal women.
21 has a negative impact on quality of life of postmenopausal women.
22 itable for application in this population of postmenopausal women.
23 idence and mortality among premenopausal and postmenopausal women.
24 compared with continuous use of letrozole in postmenopausal women.
25 d motivate programs for weight loss in obese postmenopausal women.
26 ciated with increased risk of diabetes among postmenopausal women.
27 opausal women and 61.7 (7.2) years among the postmenopausal women.
28 cancer risk factors among premenopausal and postmenopausal women.
29 women and 54.7% (95% CI, 46.5%-54.7%) among postmenopausal women.
30 nondairy, and vegetable origins) in healthy postmenopausal women.
31 higher compared to 13.8 +/- 11.8 pmol/L for postmenopausal women.
32 dence of and mortality by race/ethnicity for postmenopausal women.
33 th an increased risk of bladder cancer among postmenopausal women.
34 ine are not risk factors for hypertension in postmenopausal women.
35 in gallate (EGCG) on blood lipids in healthy postmenopausal women.
36 ted with risk of CRC in this large cohort of postmenopausal women.
37 LS mortality associated with strenuous PA in postmenopausal women.
38 were inversely associated with T2D in these postmenopausal women.
39 nal microbial communities of Black and White postmenopausal women.
40 end points in perimenopausal, menopausal, or postmenopausal women.
41 one-receptor-positive early breast cancer in postmenopausal women.
42 to determine the skeletal benefits of SCF in postmenopausal women.
43 servational Study (1993-2012), a US study of postmenopausal women.
44 her risk factors for CTS identified in these postmenopausal women.
45 ism for the increased ovarian cancer risk in postmenopausal women.
46 n on the risk of cancer in a large cohort of postmenopausal women.
47 premenopausal women but an increased risk in postmenopausal women.
48 , non-Hodgkin lymphoma, and breast cancer in postmenopausal women.
49 %, for women with no family history, and for postmenopausal women.
50 sion of the gene encoding NKB is elevated in postmenopausal women.
51 stance in black compared with white pre- and postmenopausal women.
52 is independently associated with CHIP among postmenopausal women.
53 diets could be a risk factor for insomnia in postmenopausal women.
54 ive protein levels in both premenopausal and postmenopausal women.
55 development of asthma in perimenopausal and postmenopausal women.
56 stratified by male, premenopausal women, and postmenopausal women.
57 (P = 0.01) and trochanter BMD (P = 0.007) in postmenopausal women.
58 4-wk intervention periods in 20 overweight, postmenopausal women.
59 ne (DPV) vaginal ring (VR) versus placebo in postmenopausal women.
60 efully considered before starting therapy in postmenopausal women.
61 ase were investigated in this study on older postmenopausal women.
62 ted to prevent ER(+) breast cancers in obese postmenopausal women.
63 ospective cohort of 65-y-old healthy men and postmenopausal women.
64 a composite of cardiovascular diseases among postmenopausal women.
65 ep duration is associated with longer LTL in postmenopausal women.
66 usly sedentary middle-aged and older men and postmenopausal women.
67 le in lowering endometrial cancer risk among postmenopausal women.
68 y present in plasma of obese versus nonobese postmenopausal women.
69 were safe, well tolerated, and acceptable in postmenopausal women.
72 ticenter, double-blind study of 115 healthy, postmenopausal women (45 to 75 years of age) from Novemb
73 e concentrations were measured in 80 men and postmenopausal women (48 men, 32 women, age 40-65 y) enr
74 eding trial that was conducted in 81 men and postmenopausal women [49 men and 32 women; age range: 40
76 (-11.5%; 95% CI: -15.0, -8.0; p<0.0001) and postmenopausal women (-7.2%; 95% CI: -10.0, -4.3; p<0.00
78 study was completed by 45 overweight men and postmenopausal women [age 58.9 +/- 4.3 y, BMI 27.9 +/- 1
79 onsuming a Western-style diet, 49 men and 32 postmenopausal women [age range: 40-65 y, body mass inde
80 ion, and invasive breast cancer among 12,701 postmenopausal women aged >/=50 years in a Women's Healt
83 cebo-controlled, phase 2 study, we recruited postmenopausal women aged 18 years or older with oestrog
84 domized clinical trials that involved 27 347 postmenopausal women aged 50 through 79 years with no pr
85 Observational follow-up of US multiethnic postmenopausal women aged 50 to 79 years enrolled in 2 r
87 is randomised controlled trial, we recruited postmenopausal women aged 50-74 years from 13 centres in
88 fication Trial.Participants comprised 48,835 postmenopausal women aged 50-79 y; 40% were randomly ass
91 on microsimulation model of osteoporosis for postmenopausal women aged 55 years or older was develope
92 , placebo-controlled, phase 3 FREEDOM trial, postmenopausal women aged 60-90 years with osteoporosis
93 le-blind, placebo-controlled, phase 2 trial, postmenopausal women aged at least 18 years with an East
94 3 trial (done in 130 UK hospitals) in which postmenopausal women aged at least 50 years with WHO per
95 acebo-controlled phase 2, study, we enrolled postmenopausal women (aged >=18 years) with histological
97 n's Health Initiative (WHI) enrolled 161 809 postmenopausal women, aged 50 to 79 years (mean [SD] age
98 e mortality, and other major endpoints among postmenopausal women, aged 50-79 years at HT initiation.
101 olite of DEP) concentration (p < 0.05) among postmenopausal women; all six genes loaded on to one of
102 nd 18.4%, 12.7%, and 10.5%, respectively, in postmenopausal women.An interactive program for calculat
104 BC count was measured at baseline in 160,117 postmenopausal women and again in year 3 in 74,375 parti
105 HDL function and composition in overweight, postmenopausal women and determine how changes in HDL co
106 d size in black compared with white pre- and postmenopausal women and determine the relationship betw
107 alent risk factor for both premenopausal and postmenopausal women and had the largest effect on the P
108 ctive strategy for osteoporosis screening in postmenopausal women and has the potential to prevent a
109 National Osteoporosis Foundation guidelines, postmenopausal women and men at least 50 y old with oste
112 ssociation between the facial features of 97 postmenopausal women and their levels of OS biomarkers 8
113 for the prevention of chronic conditions in postmenopausal women and whether outcomes vary among wom
114 baseline hemoglobin was measured in 160,081 postmenopausal women and year 3 hemoglobin was measured
116 ian cancer incidence is highest in peri- and postmenopausal women, and epidemiological studies have e
117 es of unmedicated naturally ovulating women, postmenopausal women, and men daily and determined urina
118 cholesterol-lowering medications.CVD risk in postmenopausal women appears to be sensitive to a change
121 , which indicates that CpdX could be used in postmenopausal women as an efficient "harmless" GC subst
122 he present study, self-reported intakes from postmenopausal women at 40 participating US clinical cen
123 estrogen receptor-positive breast cancer in postmenopausal women at increased risk for breast cancer
124 estrogen receptor-positive breast cancers in postmenopausal women at increased risk of developing bre
129 A total of 439 overweight/obese, healthy, postmenopausal women [body mass index (BMI) > 25 kg/m(2)
131 range of potential nutritional biomarkers in postmenopausal women by using a controlled feeding study
132 associations were particularly strong among postmenopausal women [ (CI: 0.57, 0.93) and (CI: 0.74, 0
133 In this secondary analysis of node-negative postmenopausal women, conducted in the era before mammog
135 tary pattern on the cardiovascular health of postmenopausal women continues to be of public health in
136 re favorable among premenopausal or recently postmenopausal women deserves further investigation.
139 cent to the fracture site were obtained from postmenopausal women during fracture repair surgery (fra
141 We prospectively examined a cohort of 93,676 postmenopausal women enrolled in the Women's Health Init
143 and HFrEF in a multiracial cohort of 42 170 postmenopausal women followed up for a mean of 13.2 year
144 h 3, 2003, and Feb 8, 2012, we enrolled 2980 postmenopausal women from 236 centres in 14 countries an
145 estionnaires between 1980 and 2014 in 75,180 postmenopausal women from the Nurses' Health Study, and
147 (CaD) and fracture risk.Data from 5823 white postmenopausal women from the Women's Health Initiative
148 alized controlled feeding study in which 153 postmenopausal women from the Women's Health Initiative
153 The molecular basis of RUTI, especially in postmenopausal women, has remained unclear because model
161 blood pressure and incident hypertension in postmenopausal women in the Women's Health Initiative Ob
162 acid fractions in breast adipose tissue for postmenopausal women in whom BMI values are not correlat
165 in a very homogeneous population of healthy postmenopausal women, indicate that there is a beneficia
169 one therapy to prevent chronic conditions in postmenopausal women is associated with some benefits, t
172 findings of higher E2 levels in men than in postmenopausal women may suggest that decreased oestroge
173 tion between MHT and risk of FI among 55,828 postmenopausal women (mean age, 73 years) who participat
174 nd slightly obese individuals (30 men and 22 postmenopausal women, mean +/- SD age: 62 +/- 6 y) were
176 cases of invasive breast cancer developed in postmenopausal women (n = 121,700) in the Nurses' Health
182 Conclusion In our observational cohort of postmenopausal women observed from 2004 to 2011, BP use,
185 plain the reduced breast cancer incidence in postmenopausal women over 60 who are taking conjugated e
191 Methods The study population included 64,438 postmenopausal women participating in the French E3N (Et
192 sonality in self-reported diet quality among postmenopausal women participating in the Women's Health
193 orectomy (BSO), and incidence of diabetes in postmenopausal women participating in the Women's Health
194 n (YM), young women (YW), older men (OM) and postmenopausal women (PMW); and (2) measured changes in
195 nd risk of colorectal cancer (CRC) in 87,042 postmenopausal women recruited from 1993-1998 by the Wom
196 ongitudinal prospective cohort evaluation of postmenopausal women recruited from 40 clinical centers.
197 group analyses revealed that high-performing postmenopausal women (relative to low and middle perform
200 Shotgun sequencing of vaginal swabs from postmenopausal women self-identified as Black or White w
202 consumption of 2 whole eggs/d by overweight, postmenopausal women showed a significant increase in ch
204 delaying or reducing PD symptoms in men and postmenopausal women.SIGNIFICANCE STATEMENT The mechanis
209 ons can be detected in this population of US postmenopausal women, these differences are not substant
210 le-blinded trial was performed in 14 healthy postmenopausal women to compare doses of 0, 10, and 20 g
211 Ab) and RNA-sequencing of bone biopsies from postmenopausal women to identify osteoclast-secreted fac
213 sis of urine and bladder biopsy samples from postmenopausal women undergoing cystoscopy with fulgurat
214 iated with serious adverse health effects in postmenopausal women, use of menopausal hormone therapy
215 CI of 2-year increments) with depression in postmenopausal women was shown for increasing age at men
217 bone mineral density (BMD) loss in peri- and postmenopausal women.We systematically searched EMBASE a
218 ional data from three independent samples of postmenopausal women were analyzed, including women from
221 02) were associated with lower CRP levels in postmenopausal women, whereas duration of OC use was pos
222 02) were associated with lower CRP levels in postmenopausal women, whereas only OC duration was posit
223 ficantly increased bone calcium retention in postmenopausal women, which improved the bone calcium ba
228 This was a prospective cohort study with postmenopausal women who participated in the Women's Hea
229 lth Initiative RA Study (1993-2010), sampled postmenopausal women who reported RA at baseline (1993-1
230 blood pressures at annual visit 3 in 29,985 postmenopausal women who were not hypertensive at baseli
232 ndometrial and ovarian cancers among 108,136 postmenopausal women who were recruited in the US Women'
236 ry prevention of chronic conditions for most postmenopausal women with an intact uterus and that estr
239 and Participants: A retrospective cohort of postmenopausal women with breast cancer diagnosed from J
240 4747 (89.8%) premenopausal and 12502 (95.1%) postmenopausal women with breast cancer had at least 1 b
241 arotid plaque composition in elderly men and postmenopausal women with carotid atherosclerosis, as we
242 study estimated rates of sexual distress in postmenopausal women with chronic insomnia and explored
246 he estrogen exposure and deprivation period, postmenopausal women with drug-naive PD were divided int
247 l to compare anastrozole versus tamoxifen in postmenopausal women with ductal carcinoma in situ under
248 e-blind, phase III trial included AI-treated postmenopausal women with early-stage breast cancer and
250 -blind trial, BIG 1-98, which enrolled 8,010 postmenopausal women with early-stage, hormone receptor-
251 bined with endocrine therapy is effective in postmenopausal women with endocrine-resistant, hormone r
252 one treatment plus 3 years of the other) for postmenopausal women with endocrine-responsive early bre
255 We used multimodal imaging to compare 26 postmenopausal women with fibromyalgia with 25 healthy c
258 ble-blind trial that randomly assigned 6,193 postmenopausal women with hormone receptor-positive earl
261 strozole offers another treatment option for postmenopausal women with hormone-receptor-positive DCIS
262 acy of anastrozole with that of tamoxifen in postmenopausal women with hormone-receptor-positive DCIS
263 than tamoxifen for preventing recurrence in postmenopausal women with hormone-receptor-positive inva
264 -line or second-line treatments, or both, in postmenopausal women with hormone-receptor-positive, HER
265 rapies with or without targeted therapies in postmenopausal women with hormone-receptor-positive, HER
267 ase 3 clinical trial (NCT00073528), in which postmenopausal women with HR-positive invasive breast ca
268 th letrozole for first-line treatment in 668 postmenopausal women with HR-positive, HER2-negative rec
270 We included 3,393 premenopausal and 3,915 postmenopausal women with intact ovaries/uterus from the
271 We included 3,393 premenopausal and 3,915 postmenopausal women with intact ovaries/uterus from the
272 ative to the standard dose for both pre- and postmenopausal women with intraepithelial neoplasia are
274 limus may be administered with exemestane to postmenopausal women with MBC whose disease progresses w
275 this randomized, open-label phase II trial, postmenopausal women with newly diagnosed operable estro
276 menopausal state confers fibrosis risk among postmenopausal women with nonalcoholic fatty liver disea
277 ime from menopause with fibrosis severity in postmenopausal women with nonalcoholic fatty liver disea
279 d Methods The trial randomly assigned 48,835 postmenopausal women with normal mammograms and without
282 -neutralizing antibody (Scl-Ab) indicated in postmenopausal women with osteoporosis at high risk for
288 rates the association between ELF and CLD in postmenopausal women with risk factors for liver disease
289 RE) and its performance in predicting LRE in postmenopausal women with risk factors in a nested case-
292 ncology Group (ACOSOG) Z1031A trial enrolled postmenopausal women with stage II or III ER-positive (A
293 n the US Pelvic Floor Disorders Network, 183 postmenopausal women with symptomatic uterovaginal prola
295 Vs) in breast cancer susceptibility genes in postmenopausal women with vs without breast cancer to gu
296 bacterial disease (PNTM) often affects white postmenopausal women, with a tall and lean body habitus
297 depression-related metabolic alterations in postmenopausal women, with possible implications for lat