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1 carriers may have an increased incidence of premature menopause.
3 at menopause 43.7 +/- 8.6 years), women with premature menopause (29.3%) were younger at enrollment (
4 MD include age, previous fragility fracture, premature menopause, a family history of hip fracture, a
7 adiotherapy, and radical surgery, can induce premature menopause and infertility in hundreds of thous
8 e women at risk for acute ovarian failure or premature menopause and men at risk for temporary or per
10 oses were at risk for acute ovarian failure, premature menopause, and small-for-gestational-age offsp
11 ramifications involved with the induction of premature menopause as well as potential benefits necess
12 enopause (at age < 47 years), 33 of whom had premature menopause (at age < 40 years), as well as amon
13 ay more limited features of aging, including premature menopause; both syndromes involve genome insta
14 he chronic effects of cancer (pain, fatigue, premature menopause, depression/anxiety), monitoring for
15 opause and a > or = 9-fold increased risk of premature menopause due to an FMR1 premutation, under a
16 ewed the frequency of acute ovarian failure, premature menopause, live birth, stillbirth, spontaneous
17 f PM and PO is low, but the complications of premature menopause may be significant, and few studies
19 early menopause and suggest that the risk of premature menopause to fragile X-premutation carriers ma
20 a > or = 26-fold increased risk of familial premature menopause, under a less probable model in whic
21 opause at age 40 or more years compared with premature menopause was associated with a 50% decreased
22 resistance, and hormone replacement therapy, premature menopause was associated with an increased lik
23 surface area (which has been associated with premature menopause) was associated with a significantly
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