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1  sole diagnostic method (despite a favorable live-birth rate).
2 mbryo transfers was associated with a higher live birth rate.
3 nificantly improve semen quality or couples' live birth rates.
4 reduce multiple gestations while maintaining live birth rates.
5 ian stimulation was associated with improved live birth rates.
6          Primary outcomes were pregnancy and live birth rates.
7 vidual women in order to estimate cumulative live-birth rates.
8  7.8 years of follow-up (risk, 2.13 per 1000 live births; rate, 2.63/10000 child-years).
9  29 years and 30 to 34 years of age, maximum live-birth rates (43 % and 36%, respectively) were achie
10            The cumulative prognosis-adjusted live-birth rate across all cycles continued to increase
11 -birth rate per IVF cycle and the cumulative live-birth rates across all cycles in all women and by a
12                                     Overall, live birth rates after BC were significantly higher amon
13 ta for predicting singleton, twin, and total live birth rates after human embryo transfer.
14 going IVF, the cumulative prognosis-adjusted live-birth rate after 6 cycles was 65.3%, with variation
15 nts undergoing 14,248 cycles, the cumulative live-birth rate after 6 cycles was 72% (95% confidence i
16               Primary outcome was cumulative live-birth rate after up to three transfers.
17                                              Live-birth rates after treatment with assisted reproduct
18 re ART treatment were associated with higher live birth rates among a population exposed to folic aci
19 ether levothyroxine treatment would increase live-birth rates among euthyroid women who had thyroid p
20                                              Live-birth rates among older women are lower than those
21                      We estimated cumulative live-birth rates among patients undergoing their first f
22                  The primary outcome was the live birth rate and secondary outcomes included gestatio
23  most severe metabolic complications, lowest live birth rates and highest PCOS remission rate; PCOS w
24              Secondary outcomes included the live-birth rate and late pregnancy complications.
25 ection trial (NCT03673592) showed equivalent live-birth rates and miscarriage rates across 484 euploi
26 y lupus during pregnancy on gestational age, live birth rate, and small for gestational age babies.
27                    Our results indicate that live-birth rates approaching natural fecundity can be ac
28 ice for women with low prognosis in terms of live birth rate compared with a freeze-all strategy.
29                                              Live-birth rates declined with increasing maternal age a
30                               The cumulative live-birth rate decreased with increasing age, and the a
31 ents), graft survival, and uterus transplant live birth rate (defined as live birth per transplanted
32                                              Live birth rate following fresh embryo transfer vs cryop
33 ally feasible and was associated with a high live birth rate following successful graft survival.
34 ogous oocytes, data have demonstrated higher live birth rates following cryopreserved-thawed embryo t
35           For women aged 40 to 42 years, the live-birth rate for the first cycle was 12.3% (95% CI, 1
36                            In all women, the live-birth rate for the first cycle was 29.5% (95% CI, 2
37 r than 40 years using their own oocytes, the live-birth rate for the first cycle was 32.3% (95% CI, 3
38            Secondary pregnancy outcomes were live birth rate, gestation, very preterm birth (<32 week
39                 Pregnancy outcomes including live birth rates, gestational age, and proportion of bab
40                                          The live birth rate in the Canadian cohort (86.4%) was signi
41 tudy showed that Zishen Yutai Pill increased live birth rates in women aged 35-42 undergoing IVF, wit
42 ections do not increase ongoing pregnancy or live-birth rates in women with unexplained RPL.
43 dless of whether embryos were cryopreserved, live-birth rates increased if more than 2 embryos were t
44 potential of preimplantation embryos and the live birth rate, it might represent a novel means to imp
45                      The primary outcome was live birth rate (LBR) following oocyte donor cycles.
46 ancy rate (CPR), secondary outcomes included live birth rate (LBR), biochemical pregnancy rate (BPR),
47 rate (IR), ongoing pregnancy rate (OPR), and live birth rate (LBR).
48 d reproductive technology (ART) face reduced live birth rates (LBR) and remain a major clinical chall
49 llowing a 50% clinical pregnancy rate with a live birth rate of 42% overall.
50 is translated into an adjusted difference in live birth rates of 26% (95% CI: 10%, 48%; P = 0.02).
51 tensity and pregnancy outcomes emerged, with live birth rates of 48% in women dialyzed </=20 hours pe
52 , P(superiority) = 0.003) (1-year cumulative live birth rates of 75.7% versus 68.9%).
53 continued due to poor prognosis and having a live-birth rate of 0 had they continued.
54 es achieving a cumulative prognosis-adjusted live-birth rate of 31.5% (95% CI, 29.7%-33.3%).
55 les achieved a cumulative prognosis-adjusted live-birth rate of 68.4% (95% CI, 67.8%-68.9%).
56 gle blastocyst transfer increases cumulative live-birth rates over single cleavage-stage transfer.
57 interest were the pregnancy, miscarriage and live birth rate per cycle.
58                                  The overall live birth rate per embryo transfer was similar to the U
59                                          The live birth rates per embryo varied from as high as 43% f
60                                              Live-birth rate per IVF cycle and the cumulative live-bi
61  of 552 women in the water group (28.1%) had live births (rate ratio, 1.38; 95% CI, 1.17 to 1.64; P<0
62                      The primary outcome was live birth rate; secondary outcomes were clinical pregna
63 stimates assumed that these women would have live-birth rates similar to those for women continuing t
64  number of embryos needed to achieve maximum live- birth rates varied by age and whether extra embryo
65                                              Live birth rate was 19.2% and lowest average SPTRX3 leve
66                                          The live birth rate was 37.2%.
67                               The cumulative live birth rate was lower in the frozen embryo transfer
68                                 However, the live birth rate was lower only for those in the first qu
69 es; moderate certainty), but their effect on live birth rates was unclear (RR, 1.15 [CI, 0.95 to 1.40
70                                          The live-birth rate was 22.5% (47 of 209 subjects) in the cl
71                                          The live-birth rate was 37.4% (176 of 470 women) in the levo
72                                          The live birth rates were 33.7% (175/520) in the time-lapse
73                                              Live-birth rates were 74.8% in blastocyst-stage group ve
74                                          The live-birth rates were 86.0% (185 of 215 women) and 86.7%
75 gnosis-adjusted, and conservative cumulative live-birth rates were estimated, reflecting 0%, 30%, and
76       Among women 35 years of age and older, live-birth rates were lower overall and regardless of wh
77 ervative and optimal estimates of cumulative live-birth rates were, respectively, 42.7% and 65.3% for
78 birth risk but was associated with increased live-birth rates when fewer embryos were transferred.
79 ovarian stimulation and a negative impact on live birth rates with fresh embryo transfer.
80 e, the conservative and optimal estimates of live-birth rates with autologous oocytes had declined fr