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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.
15 , Ecuador, and Estonia), had reduced preterm birth rates 1990-2010.
16 years of follow-up (risk, 2.13 per 1000 live births; rate, 2.63/10000 child-years).
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
21       The cumulative prognosis-adjusted live-birth rate across all cycles continued to increase up to
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
25                                          Low birth rates after A.D. 1200 mark the beginning of the de
26                                         Live-birth rates after treatment with assisted reproductive t
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
29                                         Live-birth rates among older women are lower than those among
30                 We estimated cumulative live-birth rates among patients undergoing their first fresh-
31                       Between 1980 and 1985, birth rates among teenaged girls aged 15 to 19 years dec
32                                        Lower birth rates among women with RA may at least in part ref
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
36         Secondary outcomes included the live-birth rate and late pregnancy complications.
37 paradox of steep and sustained reductions in birth rate and mortality alongside continued burdens of
38             The primary outcome was the live birth rate and secondary outcomes included gestational a
39 ssed the evidence for seasonal variations in birth rate and tested the extent to which these are subj
40         The significant correlations between birth rates and both place (latitude) and time (year of
41 lt in an increase in CRS burden for specific birth rates and coverage levels.
42                        A correlation between birth rates and disease activity and progression appears
43        It was also associated with increased birth rates and rates of abortion during the second trim
44 s disorder is growing in global relevance as birth rates and survival of babies with low gestational
45 stetric histories of subjects, study preterm birth rates and the periodontal treatment response.
46 5, notably on indicators MDG 5.4 (adolescent birth rate) and 5.6 (unmet need for family planning).
47 us during pregnancy on gestational age, live birth rate, and small for gestational age babies.
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
52               Our results indicate that live-birth rates approaching natural fecundity can be achieve
53 that robust clonal expansion, where cellular birth rates are significantly greater than death rates,
54                                           If birth rates are uniform across sites, then K </= u.
55 ell at the end of the 19th century, European birth rates began to plummet.
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
61         In order to allow for differences in birth rates, contact rates and movement rates among diff
62  disease remains a major killer in some high birth rate countries of the Sahel.
63 s a several-hundred-year period of increased birth rates coupled with stable mortality rates, resulti
64                                              Birth rates declined in all study populations in spring
65                                         Live-birth rates declined with increasing maternal age and in
66                          The cumulative live-birth rate decreased with increasing age, and the age-st
67 proportions as life expectancy increases and birth rate decreases.
68          Neither gestational age nor preterm birth rate differed with vitamin A or beta-carotene supp
69                                     However, birth rates differed in subsequent years; overall, famil
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,
73 ated depression were associated with preterm birth rates exceeding 20%.
74 s of previous studies, which assume that the birth rate exhibits a monotonic temperature response, th
75            First, when the resource species' birth rate exhibits a unimodal temperature response, as
76                                 Crude annual birth rate for 4-month survivors of SCT was lower than t
77 pated mortality benefit from a lower preterm birth rate for Blacks has been blunted by suboptimal imp
78      For women aged 40 to 42 years, the live-birth rate for the first cycle was 12.3% (95% CI, 11.8%-
79                       In all women, the live-birth rate for the first cycle was 29.5% (95% CI, 29.3%-
80 n 40 years using their own oocytes, the live-birth rate for the first cycle was 32.3% (95% CI, 32.0%-
81                                  The preterm birth rate for twins increased from 40.9% in 1981 to 55.
82  regional, and national estimates of preterm birth rates for 184 countries in 2010 with time trends f
83 al models were developed to estimate preterm birth rates for 2010.
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
86 n tree shapes, but can bias inference of the birth rate from trees.
87                          We compiled monthly birth rates from 1911 through 1930 in 3 Scandinavian cou
88                                           DC birth rates from 1999 to 2007 correlated with proxies fo
89 he genealogy as a function of the individual birth rate gamma, the individual death rate mu, and the
90            Pregnancy outcomes including live birth rates, gestational age, and proportion of babies w
91                          Those patients with birth rates greater than 0.35% per day were much more li
92                                          The birth rate has been stable since 1994.
93 on of family planning in countries with high birth rates has the potential to reduce poverty and hung
94                                     The live birth rate in the Canadian cohort (86.4%) was significan
95 ng fetal levels, and maintaining the preterm birth rate in vivo in a pregnant mouse model.
96 rmeability, and strikingly increased preterm birth rates in a mouse model of ascending vaginal infect
97                                              Birth rates in DC also increased versus Baltimore City a
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
100            The reasons for the variations in birth rates in the general population are unclear, but n
101 ns do not increase ongoing pregnancy or live-birth rates in women with unexplained RPL.
102 AS) of two fertility traits (family size and birth rate) in 269 married men who are members of a foun
103 , leading to lower fertility (that is, lower birth rates) in urban than in rural areas.
104 nsive prenatal care utilization, the preterm birth rate increased from 35.1% to 55.8%, compared with
105                                     Multiple-birth rates increased as high as 45.7% for women aged 20
106  of whether embryos were cryopreserved, live-birth rates increased if more than 2 embryos were transf
107                    Overall in the Southwest, birth rates increased slowly from 1100 B.C. to A.D. 500,
108               We confirm that seasonality in birth rate is ubiquitous and subject to highly significa
109 tial of preimplantation embryos and the live birth rate, it might represent a novel means to improve
110 vivorship, and healthy females maintain high birth rates late into life.
111                      Live-birth and multiple-birth rates may vary by patient age and embryo quality.
112 ife histories, Darwinian fitness is equal to birth rate minus death rate.
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
115                 However, neither the preterm birth rate nor the rate of long-term neurologic disabili
116 n the context of this variation we show that birth rates observed in typical case collections are hig
117             Furthermore, the highest preterm birth rates occur in low-income settings where the cause
118 nued due to poor prognosis and having a live-birth rate of 0 had they continued.
119 hieving a cumulative prognosis-adjusted live-birth rate of 31.5% (95% CI, 29.7%-33.3%).
120 ng a 50% clinical pregnancy rate with a live birth rate of 42% overall.
121 chieved a cumulative prognosis-adjusted live-birth rate of 68.4% (95% CI, 67.8%-68.9%).
122                                 Finally, the birth rate of apoB-27.6 homozygotes (Apob(27.6/27.6)) fr
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.
125                        However, the very low birth rate of SC pups limits practical use of this appro
126 al stage and seasonal forcing applied to the birth rate of the host.
127 anslated into an adjusted difference in live birth rates of 26% (95% CI: 10%, 48%; P = 0.02).
128 ty and pregnancy outcomes emerged, with live birth rates of 48% in women dialyzed </=20 hours per wee
129 ve target of a relative reduction in preterm birth rates of 5% by 2015.
130 ve target of a relative reduction in preterm birth rates of 5% by 2015.
131              The impact of trends in preterm birth rates on neonatal and infant mortality was also ev
132 x vaccination had no effect on pregnancy and birth rates or adverse birth outcomes.
133 age group, trends in pregnancy, abortion and birth rates over the decade were similar to those for ol
134                             The overall live birth rate per embryo transfer was similar to the US nat
135                                         Live-birth rate per IVF cycle and the cumulative live-birth r
136                      Live-birth and multiple-birth rates (percentage of live births that were multipl
137                                  To maximize birth rates, physicians who perform in vitro fertilizati
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
142 ping MS coincide with the lowest and highest birth rates, respectively.
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
145                 Trends in teen pregnancy and birth rates show continued decline, but state and racial
146                         Chimpanzee and human birth rates show similar patterns of decline beginning i
147 tes assumed that these women would have live-birth rates similar to those for women continuing treatm
148       The decline in under-18 conception and birth rates since 1998 and evidence that the declines ha
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
155                                     Multiple-birth rates varied by age and the number of embryos tran
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
158                             The crude 3-year birth rate was 11.0 per 1000.
159                                         Live birth rate was 19.2% and lowest average SPTRX3 levels we
160                                     The live-birth rate was 22.5% (47 of 209 subjects) in the clomiph
161 mong women aged 35 to 39 years, the multiple-birth rate was 29.4% if 3 embryos were transferred.
162                                     The live birth rate was 37.2%.
163 e death rate was 43.2 per 1000 and the crude birth rate was 8.8 per 1000.
164                  Second, the overall preterm birth rate was higher among Mexican Americans (10.6%) th
165               The rate of cell cycle or cell birth rate was increased by 29% (P<0.05) in cells overex
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
169         With 2 embryos transferred, multiple-birth rates were 22.7%, 19.7%, 11.6%, and 10.8% for wome
170                                     The live-birth rates were 86.0% (185 of 215 women) and 86.7% (183
171                                              Birth rates were calculated from the kinetic profiles.
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
174                                          Low birth rates were observed in survivors after advanced-st
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).
177  risk but was associated with increased live-birth rates when fewer embryos were transferred.
178 e conservative and optimal estimates of live-birth rates with autologous oocytes had declined from 63

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