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1 primary and secondary amenorrhoea as well as early menopause.
2 point was incidence of chemotherapy-induced early menopause.
3 eatments except MTX-FA increased the risk of early menopause.
4 rooctanoate (PFOA) have been associated with early menopause.
5 ent loss in osteopenic/osteoporotic women in early menopause.
6 ering the risk of both sporadic and familial early menopause.
7 fore and they are at risk of the sequelae of early menopause.
8 be modestly associated with a lower risk of early menopause.
9 (hazard ratio, 2.45; 95% CI, 1.33 to 4.54); early menopause, 5.1% vs. 1.7% (hazard ratio, 2.35; 95%
10 t a > or = 4-fold increased risk of familial early menopause and a > or = 26-fold increased risk of f
11 o rule out a > or = 3-fold increased risk of early menopause and a > or = 9-fold increased risk of pr
13 gainst ovarian failure, reducing the risk of early menopause and improving prospects for fertility.
14 rmation on the prevalence of anovulation and early menopause and on pituitary-gonadal function among
15 X premutation is not a major risk factor for early menopause and suggest that the risk of premature m
18 for premutation alleles among 216 women with early menopause (at age < 47 years), 33 of whom had prem
20 on, a significant number of women experience early menopause due to oophorectomy performed for benign
24 whether an average of 5.4 years of HT during early menopause has longer term protective effects on gl
26 ith a borderline significantly lower risk of early menopause (HR: 0.87; 95% CI: 0.76, 1.00; P-trend =
27 ies have shown decreased pregnancy rates and early menopause in female cancer survivors; however, inf
28 calcium are associated with the incidence of early menopause in the prospective Nurses' Health Study
32 en for whom progesterone levels were tested; early menopause occurred in 2 (8%) of 24 women for whom
33 multiple birth was strongly associated with early menopause (odds ratio = 1.42, confidence interval:
35 typed gonadotropin alterations indicative of early menopause, poor oocyte quality, and infertility.
37 evere if the donors were in late rather than early menopause suggested that new progenitor phenotypes
38 28 IU/d) had a significant 17% lower risk of early menopause than women with the lowest intake [quint
40 lemia, hyperuricemia, diabetes, obesity, and early menopause were each associated with a higher risk
42 beneficial effect on the heart if started in early menopause, when a woman's arteries are still likel
43 d an association between multiple births and early menopause, which connects events pre-birth, when t
44 ntakes of vitamin D and calcium and incident early menopause while accounting for potential confoundi
45 g women at higher risk for depression due to early menopause who could benefit from psychiatric inter
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