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1 diagnostic method (despite a favorable live-birth rate).
2 or have not consistently reduced the preterm birth rate.
3 n interactions to include seasonality in the birth rate.
4 this respect and must have a lower intrinsic birth rate.
5 in the tumor and the age-dependent cellular birth rate.
6 increasing life expectancy and a decreasing birth rate.
7 d stable, resulting in a 26% increase in the birth rate.
8 mice born during the M-SOB with the highest birth rate.
9 ers have significantly higher copulation and birth rates.
10 e multiple gestations while maintaining live birth rates.
11 ue to high maternal HSV-2 infection and high birth rates.
12 d sub-Saharan Africa has the highest preterm birth rates.
13 51 978 MS patients were compared to expected birth rates.
14 l women in order to estimate cumulative live-birth rates.
17 465 children with a diagnosis, 14 were twin births (rate 30.0/1,000) compared to 9,640 children of m
18 ears and 30 to 34 years of age, maximum live-birth rates (43 % and 36%, respectively) were achieved w
19 hich we then replace with the time dependent birth rate a(t), to investigate how this effects the dyn
20 f the model with a constant time-independent birth rate, a, which we then replace with the time depen
22 h rate per IVF cycle and the cumulative live-birth rates across all cycles in all women and by age an
23 IVF, the cumulative prognosis-adjusted live-birth rate after 6 cycles was 65.3%, with variations by
24 ndergoing 14,248 cycles, the cumulative live-birth rate after 6 cycles was 72% (95% confidence interv
27 Among these sexually experienced teenagers, birth rates also declined between 1980 and 1985 and then
28 T treatment were associated with higher live birth rates among a population exposed to folic acid for
33 ation cannot persist no matter how large its birth rate, an effect not seen in previous simpler model
34 nistration significantly reduced the preterm birth rate and altered placental immune profile with dec
35 k women, for example, have twice the preterm birth rate and higher rates of growth restriction than d
37 paradox of steep and sustained reductions in birth rate and mortality alongside continued burdens of
39 ssed the evidence for seasonal variations in birth rate and tested the extent to which these are subj
44 s disorder is growing in global relevance as birth rates and survival of babies with low gestational
46 5, notably on indicators MDG 5.4 (adolescent birth rate) and 5.6 (unmet need for family planning).
48 011 were used to determine national multiple birth rates, and data on in vitro fertilization (IVF) fr
49 of peak pandemic exposure and depressions in birth rates, and identified pregnancy stages at risk of
50 identified periods of unusually low or high birth rates, and quantified births as "missing" or "in e
51 graphic transition, as a result of declining birth rates, and reduced measles prevalence, due to impr
53 that robust clonal expansion, where cellular birth rates are significantly greater than death rates,
56 on dry or rainfed farming experienced higher birth rates but less initial sociopolitical complexity.
57 pendent societies experienced relatively low birth rates but were quick to achieve a high degree of s
58 etrics, gestational weight gain, and preterm birth rate, but not in maternal age, parity, socioeconom
59 data shows that spatiotemporal variation in birth rate can explain the timing of rotavirus epidemics
60 CSI use was associated with a lower multiple birth rate compared with conventional IVF (30.9% vs 34.2
63 s a several-hundred-year period of increased birth rates coupled with stable mortality rates, resulti
70 mined the relationship between influenza and birth rates during the 1918 pandemic in the United State
71 pected when comparing such a collection with birth rates estimated by averaging population-specific n
72 f the total population by age and sex, crude birth rate, estimated prevalence of active tuberculosis,
74 s of previous studies, which assume that the birth rate exhibits a monotonic temperature response, th
77 pated mortality benefit from a lower preterm birth rate for Blacks has been blunted by suboptimal imp
80 n 40 years using their own oocytes, the live-birth rate for the first cycle was 32.3% (95% CI, 32.0%-
82 regional, and national estimates of preterm birth rates for 184 countries in 2010 with time trends f
84 regnancy in the United States, pregnancy and birth rates for that group continue to be the highest am
85 predicted a 5% relative reduction of preterm birth rate from 9.59% to 9.07% of livebirths: smoking ce
89 he genealogy as a function of the individual birth rate gamma, the individual death rate mu, and the
93 on of family planning in countries with high birth rates has the potential to reduce poverty and hung
96 rmeability, and strikingly increased preterm birth rates in a mouse model of ascending vaginal infect
98 g a set of dominance parameters which affect birth rates in each social level and movement rates betw
99 worldwide and persistently high ART multiple-birth rates in several countries highlight the need for
102 AS) of two fertility traits (family size and birth rate) in 269 married men who are members of a foun
104 nsive prenatal care utilization, the preterm birth rate increased from 35.1% to 55.8%, compared with
106 of whether embryos were cryopreserved, live-birth rates increased if more than 2 embryos were transf
109 tial of preimplantation embryos and the live birth rate, it might represent a novel means to improve
113 nual cycles tended to have higher per capita birth rates, more household crowding, more children per
114 e ability, the form with the lower intrinsic birth rate must be compensated by a more than proportion
116 n the context of this variation we show that birth rates observed in typical case collections are hig
123 Our results suggest that there is a high birth rate of new miRNA genes, accompanied by a comparab
124 n rising to large numbers, despite their low birth rate of one offspring every seven to nine days.
128 ty and pregnancy outcomes emerged, with live birth rates of 48% in women dialyzed </=20 hours per wee
133 age group, trends in pregnancy, abortion and birth rates over the decade were similar to those for ol
138 52 women in the water group (28.1%) had live births (rate ratio, 1.38; 95% CI, 1.17 to 1.64; P<0.001)
139 countries with VHHDI achieved annual preterm birth rate reductions of the best performers for 1990-20
140 countries with VHHDI achieved annual preterm birth rate reductions of the best performers for 1990-20
141 dynamics for industrialized countries, high birth rate regions should experience regular annual epid
143 rental notification law in early pregnancy), birth rates rose by 4 percent relative to those of teens
144 ontact, our results suggest that even in low birth rate settings high vaccine coverage must be mainta
147 tes assumed that these women would have live-birth rates similar to those for women continuing treatm
149 e disparity countered the changes in preterm birth rates so that the percentage decline in neonatal m
150 y rates in children younger than 5 years and birth rates, the numbers of deaths by cause were calcula
151 ly 2 decades of declining teen pregnancy and birth rates, the problem persists, with significant disp
152 op progressive disease than those with lower birth rates Thus, B-CLL is not a static disease that res
153 cidence in women aged 15-49 years to 2010-15 birth rates to estimate infections during pregnancy.
154 y and quantity of data, we estimated preterm birth rates using country-level loess regression for 201
156 r of embryos needed to achieve maximum live- birth rates varied by age and whether extra embryos were
157 patient had definable and often substantial birth rates, varying from 0.1% to greater than 1.0% of t
161 mong women aged 35 to 39 years, the multiple-birth rate was 29.4% if 3 embryos were transferred.
166 ng women 40 to 44 years of age, the multiple-birth rate was less than 25% even if 5 embryos were tran
167 us, marital status, living arrangements, and birth rate were compatible with normal living patterns.
168 t were born during the M-SOB with the lowest birth rate were less susceptible to EAE than mice born d
172 s-adjusted, and conservative cumulative live-birth rates were estimated, reflecting 0%, 30%, and 100%
173 Among women 35 years of age and older, live-birth rates were lower overall and regardless of whether
175 ive and optimal estimates of cumulative live-birth rates were, respectively, 42.7% and 65.3% for tran
176 64 type II MADS-box genes, implying a higher birth rate when compared with Arabidopsis (64 vs.47).
178 e conservative and optimal estimates of live-birth rates with autologous oocytes had declined from 63
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