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1 th (type I) but could also without (type II) premature ovarian failure.
2 display abnormal follicular development and premature ovarian failure.
3 re unable to recover and are sterile, due to premature ovarian failure.
4 mice were subfertile and exhibited signs of premature ovarian failure.
5 characterized with craniofacial defects and premature ovarian failure.
6 mutation can further develop parkinsonism or premature ovarian failure.
7 utism, FXTAS in older males and females, and premature ovarian failure.
8 in milder and more common conditions such as premature ovarian failure.
9 nd motor deterioration often associated with premature ovarian failure.
10 effects of chemotherapy and radiotherapy is premature ovarian failure.
11 epletion of the ovarian reserve and leads to premature ovarian failure.
12 erated follicular initiation plays a role in premature ovarian failure, a common cause of infertility
13 rovide insight into the causes of idiopathic premature ovarian failure, a disease that burdens many i
14 eservation in young women facing the risk of premature ovarian failure and infertility as a sequel to
15 wild-type female mice, the event that drives premature ovarian failure and infertility in female canc
16 t prenatal exposure of females to BaP causes premature ovarian failure and ovarian tumorigenesis and
17 n disease (AOD) is a probable cause of human premature ovarian failure, and a potential complication
18 letion caused ovulation of immature oocytes, premature ovarian failure, and compromised female fecund
19 esis, have increased destruction of oogonia, premature ovarian failure, and ovarian tumorigenesis aft
21 with autism spectrum disorder in childhood, premature ovarian failure, and the neurodegenerative dis
22 havioral deficits on the fragile-X spectrum; premature ovarian failure; and a newly described, neurod
25 d increased risk for cardiomyopathy, stroke, premature ovarian failure, chronic liver disease, and re
26 ccupational ovotoxicants plays a role in the premature ovarian failure commonly associated with infer
28 RanBPM homozygous mutant females displayed a premature ovarian failure due to a depletion of the germ
29 ollowing clinical end points: development of premature ovarian failure, end-stage renal disease (ESRD
30 hat a subset of Chinese women with sporadic, premature ovarian failure harbor mutations in FIGLA.
32 s may be valuable for predicting the risk of premature ovarian failure in lupus nephritis patients tr
33 induce autoimmune ovarian disease (AOD) and premature ovarian failure in neonatal, but not adult, mi
34 of chemotherapy and radiation may result in premature ovarian failure in premenopausal oncology pati
39 ity for young women who are facing a risk of premature ovarian failure (POF) caused by radiation or c
40 t mutation or an SNP on MCM8 associated with premature ovarian failure (POF) diminishes the functiona
41 a large consanguineous family with inherited premature ovarian failure (POF) identified a homozygous
42 (GnRHa) did not prevent chemotherapy-induced premature ovarian failure (POF) in patients with lymphom
43 FOXL2 mutations cause gonadal dysgenesis or premature ovarian failure (POF) in women, as well as eye
49 stimated the impact of treatment regimens on premature ovarian failure (POF) occurrence and motherhoo
52 had a significantly lower risk of developing premature ovarian failure (relative risk 0.10; 95% confi
53 mprising myopathy; demyelinating neuropathy; premature ovarian failure; short stature; hearing loss;
55 r results in relation to models that ascribe premature ovarian failure to interruption of ovarian gen
56 a large consanguineous family with inherited premature ovarian failure, we identified a homozygous 1-