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1 c used to relieve the negative components of perimenopause.
2 rement in SDMT learning observed during late perimenopause.
3 t of depression was temporally linked to the perimenopause.
4 rate enough by itself to rule in or rule out perimenopause.
5 such as hot flashes, certainly begin in the perimenopause.
6 c estradiol levels underpinned depression in perimenopause.
7 en level occur with greater magnitude during perimenopause.
9 nea events per hour were 1.2 (0.7, 2.2) with perimenopause and 2.6 (1.4, 4.8) with postmenopause; odd
10 nea events per hour were 1.1 (0.5, 2.2) with perimenopause and 3.5 (1.4, 8.8) with postmenopause.
11 failure (AOF) successfully replicates human perimenopause and postmenopause, including estrous acycl
13 63-0.96) but not in all other (premenopause, perimenopause, and unknown status) menopausal groups (n=
14 osis progression rate was accelerated during perimenopause, as shown using FIB-4 (0.12 units per year
16 rual cycle markers to determine inception of perimenopause, defined as time from study enrollment to
17 SH, the levels of which are high during late perimenopause, directly stimulates bone resorption by os
18 he basis of symptom profile, duration of the perimenopause, endocrine measures, or past historical va
19 This issue provides a clinical overview of Perimenopause focusing on prevention, diagnosis, treatme
20 riods (i.e., a window of opportunity) during perimenopause for restoring ovarian hormones for the mos
25 ood disorders, and it has been proposed that perimenopause is also a window of risk for processes lin
27 data suggest that events related to the late perimenopause may be associated with an increased suscep
29 related migraine, pregnancy, breast-feeding, perimenopause, menopause, nitric oxide, and estrogen rec
30 tory of depression had 1.2 times the rate of perimenopause of women with no such history (95% confide
32 dysphoric mood are associated with the early perimenopause, particularly among women with lower educa
36 .04), whereas women who transitioned to late perimenopause showed a 0.93-kg decline in grip strength
37 ning rate was 1.00 point smaller during late perimenopause than during premenopause (P = 0.04); furth
39 reducing the rise in LDL cholesterol during perimenopause to postmenopause but could not completely
42 did and did not become depressed during the perimenopause were determined by Student's t test, chi-s
43 that presented data relevant to diagnosis of perimenopause were identified in a MEDLINE search from 1
44 Women who developed depression during the perimenopause were not distinguished from those who rema
45 history of major depression who entered the perimenopause were twice as likely to develop significan
46 of Reproductive Aging Workshop criteria for perimenopause, which is mainly based on menstrual cycle
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