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1  cases of pSBI diagnosed for each associated neonatal death.
2 Cs results in severe mid-facial clefting and neonatal death.
3 weight for gestational age), stillbirth, and neonatal death.
4 a CI subunit, cause severe CI deficiency and neonatal death.
5 severe microcephaly, small somatic size, and neonatal death.
6 y impaired inspiratory rhythm and pronounced neonatal death.
7 a is associated with increased risk of early neonatal death.
8 rity are amongst the strongest predictors of neonatal death.
9 ion, 0.252-0.552) were the leading causes of neonatal death.
10 D die as a TOFPA, late fetal death, or early neonatal death.
11 lting in incomplete villus morphogenesis and neonatal death.
12 reterm birth, low birth weight, and fetal or neonatal death.
13 ated with an increased risk of stillbirth or neonatal death.
14 nd lens degeneration, brain hemorrhages, and neonatal death.
15 racic cavity, leading to lung hypoplasia and neonatal death.
16 , hindbrain, and inner ear deficiencies, and neonatal death.
17 demia, which is sufficiently severe to cause neonatal death.
18 k for preterm birth, very preterm birth, and neonatal death.
19 ported that homozygous (MTPa-/-) mice suffer neonatal death.
20  and its ablation results in exencephaly and neonatal death.
21 ng of some breeding pairs, renal failure and neonatal death.
22 however, dramatic neurodegeneration leads to neonatal death.
23  been shown to cause severe dwarfism but not neonatal death.
24 e embryo growth retardation, fetal loss, and neonatal death.
25 and physical disabilities and often leads to neonatal death.
26 opathy, hepatic lipid accumulation and early neonatal death.
27 e LPL did not rescue LPL knock-out mice from neonatal death.
28 1 gene have delayed parturition resulting in neonatal death.
29  exclusively in liver rescued LPL0 mice from neonatal death.
30 eted allele exhibit similar deficiencies and neonatal death.
31 mphocyte development and a high frequency of neonatal death.
32 the genetic basis of severe microcephaly and neonatal death.
33 defined as the combination of stillbirth and neonatal death.
34 estational age, miscarriage, stillbirth, and neonatal death.
35 rative skin conditions and for stillbirth or neonatal death.
36  oxygen supplementation necessary to prevent neonatal death.
37 s in altered epithelial cell homeostasis and neonatal death.
38 ultiorgan pathologies, vascular defects, and neonatal death.
39 l abnormalities, seven stillbirths, and nine neonatal deaths.
40 munity care at 90% coverage averts 18-37% of neonatal deaths.
41 uld provide a cost-effective way of reducing neonatal deaths.
42  undergoing a trial of labor), including two neonatal deaths.
43 tion, and a small group of causes leading to neonatal deaths.
44  PrP that otherwise cause many embryonic and neonatal deaths.
45                                There were no neonatal deaths.
46 s, blindness, encephalitis, and occasionally neonatal deaths.
47 re a leading cause of the 2.9 million annual neonatal deaths.
48 lth surveys for information on the timing of neonatal deaths.
49 83% of all maternal deaths, stillbirths, and neonatal deaths.
50 w birth weight (0.68; .29-1.57) and fetal or neonatal death (0.24; .04-1.52).
51 1.4%), intrauterine fetal demise (2.8%), and neonatal death (1.4%).
52 tal interventions by 2025 could avert 71% of neonatal deaths (1.9 million [range 1.6-2.1 million]), 3
53  1.00-1.35; I2 = 93.7%; n = 11 studies); for neonatal death, 1.15 (95% CI, 1.07-1.23; I2 = 78.5%; n =
54 y between groups (six [2.0%] vs three [1.0%] neonatal deaths; 1.0, -1.04 to 2.97; p=0.322).
55 5% confidence interval (CI): 1.23, 4.17) for neonatal death, 2.44 (95% CI: 1.76, 3.37) for respirator
56 on deaths in 2010, consisting of 3.1 million neonatal deaths, 2.3 million postneonatal deaths, and 2.
57 (95% CI, 67-81), and 86 (95% CI, 76-98); for neonatal death, 20, 21 (95% CI, 19-23), and 24 (95% CI,
58 d RR of 359.4 (95% CI 277.3-465.9) for early neonatal death, 30.5 (18.0-51.6) for late neonatal death
59 %), 4 premature deliveries (3%), and 1 early neonatal death; 38 deliveries (36%) were by cesarean sec
60 0 early fetal deaths and stillbirths, 62 000 neonatal deaths, 44 000 preterm or low weight births, an
61 te outcome (105/408 [26%] vs 115/419 [27%]), neonatal death (47/449 [11%] vs 58/449 [13%]), severe IV
62        Thus, 67 000 maternal deaths, 440 000 neonatal deaths, 473 000 child deaths, and 564 000 still
63  participants; OR, 0.43; 95% CI, 0.19-0.99), neonatal death (5 studies, 374 participants; OR, 0.26; 9
64 ths (total about 290,000) and stillbirths or neonatal deaths (5.5 million) occur every year.
65   In eight of the 13 countries with the most neonatal deaths (55% worldwide), we undertook a systemat
66                  In a Scotland-wide study of neonatal deaths, 70 brains have been examined.
67 CNS-specific knockout of Ufm1 in mice causes neonatal death accompanied by microcephaly and apoptosis
68                                     In 2013, neonatal deaths accounted for 41.6% of under-5 deaths co
69 tio [OR], 1.17; 95% CI, 0.96-1.41; P = .12), neonatal death (adjusted OR, 1.23; 95% CI, 0.96-1.57; P
70 ity was associated with an increased odds of neonatal death after adjustment for confounding factors
71           During the same period, the OR for neonatal death after preeclamptic pregnancy remained rel
72                      Every year about 70% of neonatal deaths (almost 3 million) happen because effect
73 l age, very low birthweight, miscarriage, or neonatal death, although few data were available for the
74 lestasis (due to Abcb11 deficiency) produces neonatal death among all offspring within 24 h of birth
75 no reports of maternal death, stillbirth, or neonatal death among the donors.
76  Study (CCSS), of the risk of stillbirth and neonatal death among the offspring of men and women who
77  was a composite of intrapartum fetal death, neonatal death, an Apgar score of 3 or less at 5 minutes
78                          Raf deletion caused neonatal death and a significant expansion of the hypert
79     The primary outcome was the composite of neonatal death and any of several adverse events, includ
80  neonatal hypoxia-ischemia, a major cause of neonatal death and pediatric disability.
81 ary neonatal composite outcome that included neonatal death and serious neonatal complications (14.3%
82  care for patients experiencing miscarriage, neonatal death and stillbirth as part of their work.
83   Sub-Saharan Africa had the highest risk of neonatal death and, therefore, had the highest risk of d
84                     A quarter of the world's neonatal deaths and 15% of maternal deaths happen in Ind
85                           Of the 3.7 million neonatal deaths and 3.3 million stillbirths each year, 9
86 ies do not get a birth certificate, and most neonatal deaths and almost all stillbirths have no death
87                     However, less than 5% of neonatal deaths and even fewer stillbirths have death re
88 the biggest risk factor for more than 80% of neonatal deaths and increases risk of post-neonatal mort
89 tillbirth), and the secondary endpoints were neonatal deaths and malformations.
90 al homoplasmic mutation that resulted in six neonatal deaths and one surviving child with Leigh syndr
91 o meet Every Newborn targets of ten or fewer neonatal deaths and ten or fewer stillbirths per 1000 bi
92 nd pneumonia were not accelerated, causes of neonatal deaths and undernutrition were not addressed, a
93     Safety outcomes were deaths in utero and neonatal deaths and were assessed in all randomly alloca
94 wth restriction, which increases the risk of neonatal deaths and, for survivors, of stunting by 2 yea
95 ly neonatal death, 30.5 (18.0-51.6) for late neonatal death, and 50.2 (42.8-59.0) for infant death.
96 ted mothers on the end points of stillbirth, neonatal death, and congenital syphilis were obtained fr
97 onal-age infants, preterm birth, stillbirth, neonatal death, and major congenital malformations.
98                     The risks of stillbirth, neonatal death, and perinatal death increased with the a
99 t smoking increases the risks of stillbirth, neonatal death, and perinatal death.
100 complications in labour carry a high risk of neonatal death, and poverty is strongly associated with
101 ernal deaths, 849 000 stillbirths, 1 498 000 neonatal deaths, and 1 515 000 additional child deaths.
102 ths, more than 4311 perinatal deaths, 11,294 neonatal deaths, and 4983 infant deaths were included.
103 of half a million maternal deaths, 4 million neonatal deaths, and 6 million child deaths.
104 um stillbirths, end preventable maternal and neonatal deaths, and improve child development.
105       We identified births, stillbirths, and neonatal deaths, and interviewed mothers 6 weeks after d
106 t encompassed eclampsia, preeclampsia, fetal/neonatal deaths, and small litter sizes occurred in some
107  risk of stillbirth, very preterm birth, and neonatal death; and ZDV-3TC-LPV-R was associated with hi
108 s in the study, 6054 were stillbirths; 3609, neonatal deaths; and 1578, postneonatal deaths.
109 aths, 531,000 stillbirths, and 1.325 million neonatal deaths annually by 2020 at an estimated running
110 ternal undernutrition contributes to 800,000 neonatal deaths annually through small for gestational a
111  many as 163 513 maternal deaths and 803 129 neonatal deaths annually.
112 revalence rate ratio [aPRR] 1.19, P = .8) or neonatal death (aPRR 0.68, P = .6).
113          Globally, the main direct causes of neonatal death are estimated to be preterm birth (28%),
114 ncluding the east African region, a third of neonatal deaths are due to infections.
115                        Reducing maternal and neonatal deaths are important global health priorities.
116                       The highest numbers of neonatal deaths are in south-central Asian countries and
117                                        Early neonatal deaths are sometimes under-reported or might be
118                             Almost all (99%) neonatal deaths arise in low-income and middle-income co
119 ount for a quarter of the 2.8 million annual neonatal deaths, as well as approximately 3% of all disa
120 ic conditions, whereas the relative risk for neonatal death associated with maternal affective disord
121 on 2 families with a history of in utero and neonatal deaths associated with nonimmune hydrops fetali
122 ere 0.68 million (0.46 million-0.92 million) neonatal deaths associated with pSBI in 2012.
123 -two infants were born prematurely; with one neonatal death at 6 weeks.
124 gnificantly increased risk of stillbirth and neonatal death at doses greater than 10.00 Gy (five [18%
125 resulting in a decrease in the percentage of neonatal death attributable to SGA.
126 premature births, small full-term births, or neonatal deaths between the 3 groups.
127                       APOs included fetal or neonatal death; birth before 36 weeks due to placental i
128 r and pancreatic beta cells are rescued from neonatal death, but develop lipoatrophic diabetes and di
129        Boys have a higher biological risk of neonatal death, but girls often have a higher social ris
130  newborns against preterm delivery and early neonatal death, but the impact beyond the neonatal perio
131 We have rescued the PTHrP-knockout mice from neonatal death by transgenic expression of PTHrP targete
132  to reduce maternal deaths, stillbirths, and neonatal deaths by 2025 in all countries tested.
133 rage of essential interventions would reduce neonatal deaths by an estimated 71%, benefit women and c
134 nnual number of stillbirths by up to 64,000, neonatal deaths by up to 25,000, and annual incidence of
135 e primary outcome measure was a composite of neonatal death, chronic lung disease, or major cerebral
136 l age had just three times the likelihood of neonatal death compared to babies born term, (OR 3.2 [95
137 mpact of universal screening on stillbirths, neonatal deaths, congenital syphilis, and disability-adj
138  abnormal renal arterial tree patterning and neonatal death consistent with kidney dysfunction.
139 cent achievements to reduce child mortality, neonatal deaths continue to remain high, accounting for
140  lowest HDI, 61% of all maternal, fetal, and neonatal deaths could be prevented.
141                             Mice that escape neonatal death develop abnormal chemoresponsiveness as a
142 rence 0.3%, 95% CI -0.8 to 1.5; p=0.566) and neonatal deaths did not differ significantly between gro
143 ratory system, loss of Hoxa5 function causes neonatal death due to respiratory distress.
144  infants to assess which test best predicted neonatal death during the first 28 days after birth.
145                                    The early neonatal death (ENND) rate declined 12% between 1996 and
146                However, the relative risk of neonatal death following a preeclamptic pregnancy has no
147 icant reduction from baseline in the rate of neonatal death from all causes in the 7 days after birth
148 on is about double the risk of stillbirth or neonatal death from intrapartum uterine rupture.
149                       As an estimated 23% of neonatal deaths globally are due to infectious causes, m
150 up to 15% of an estimated 3.3 million annual neonatal deaths globally.
151                            Three-quarters of neonatal deaths happen in the first week--the highest ri
152 d encourage reappraisal of care during which neonatal death has occurred.
153 grams of even the most severe outcome, fetal/neonatal death, has led to a lack of understanding about
154                  Although almost half of all neonatal deaths identified met minimum IDS criteria, mos
155 ated the absolute reductions in maternal and neonatal deaths if countries with low CDR increased thei
156 ience a considerably increased likelihood of neonatal death in East Africa.
157 ous substances on Earth and a major cause of neonatal death in nonvaccinated areas.
158 y affecting skeletal muscles that results in neonatal death in severe cases as a result of associated
159 hether maternal obesity is a risk factor for neonatal death in sub-Saharan Africa and the effect on t
160                                  The risk of neonatal death in term infants with five-minute Apgar sc
161                                  The rate of neonatal death in the 7 days after birth did not decreas
162 ters, there was no reduction in the rates of neonatal death in the 7 days after birth, stillbirth, or
163                      The primary outcome was neonatal death in the first 7 days after birth.
164 ge, termination of pregnancy, stillbirth, or neonatal death in the metformin group (n=7) versus the p
165 changes affecting the risk of stillbirth and neonatal death in the offspring of men exposed to gonada
166                   We calculated maternal and neonatal deaths in 2013 and 2012, respectively, for coun
167 uced litter size, and increased incidence of neonatal deaths in offspring.
168                               There were 230 neonatal deaths in the Newhints zones compared with 252
169 le logistic regression to assess the risk of neonatal death (in women's most recent singleton livebir
170 ow the 75th percentile, however, the rate of neonatal death increased from 0.03 percent in the refere
171                  We excluded stillbirths and neonatal deaths, infants whose mothers died, those with
172                            The risk of early neonatal death is very high across a range of countries
173                    Early success in averting neonatal deaths is possible in settings with high mortal
174                        The maximum effect on neonatal deaths is through interventions delivered durin
175 cy increases the incidence of stillbirth and neonatal death, leads to structural defects in the place
176                  Enzyme replacement prevents neonatal death, liver damage, and osteoporosis in murine
177 cy were prospectively related to fetal loss, neonatal death, low birth weight, preterm birth, and MTC
178 percentile of weight for gestational age) or neonatal death (<28 days from delivery), and any severe
179 here were no stillbirths and fewer than five neonatal deaths (<2.7%) in affected pregnancies compared
180 nsent (2%), a test was not done due to early neonatal death (n=13), mother departing before venesecti
181 (both in the Foley catheter group) and eight neonatal deaths (n=5 in the misoprostol group and n=3 in
182 ed ovum, n=1; intrauterine death, n=2; early neonatal death, n=1; and neonatal death, n=2).
183 e death, n=2; early neonatal death, n=1; and neonatal death, n=2).
184 ers is essential to achieve the reduction in neonatal deaths needed to meet the Millennium Developmen
185 range of adverse outcomes including fetal or neonatal death, neurodisability, and lifelong risks to t
186  (PTD), small for gestational age (SGA), and neonatal death (NND).
187 all-for-gestational-age births, or fetal and neonatal deaths; nor did it increase urolithiasis during
188  of pregnancies; fetal death occurred in 4%, neonatal death occurred in 1%, preterm delivery occurred
189                                          One neonatal death occurred.
190                              Stillbirths and neonatal deaths occurred among 7 MRI-exposed vs 9844 une
191 l and 1 117 257 (95% CI 1 033 611-1 200 902) neonatal deaths occurred in 45 countries with low CDRs i
192                                    52% of 87 neonatal deaths occurred in preterm or small for gestati
193                  1.00 million (36.3%) of all neonatal deaths occurred on day 0 (uncertainty range 0.9
194 n exposed to this strategy, an excess of 3.5 neonatal deaths occurred, and the risk of maternal infec
195    12 fetuses (2%) died in utero and 27 (6%) neonatal deaths occurred.
196 al obesity was a significant risk factor for neonatal deaths occurring during the first 2 days of lif
197 s <1 month of age, with approximately 86% of neonatal deaths occurring in low- and lower-middle-incom
198 these results suggest an explanation for the neonatal death of homozygous Lc animals.
199 ound metabolic disorder that resulted in the neonatal deaths of numerous siblings.
200 in enlargement, hyperactivation of mTOR, and neonatal death on P0 due to reduced pup-maternal interac
201 .21, 0.77; P = 0.005) but was also shown for neonatal deaths on days 1-30 of life (aHR: 0.69; 95% CI:
202 ly decrease or increase the risk of fetal or neonatal death or serious neonatal morbidity, as compare
203  primary outcome was a composite of fetal or neonatal death or serious neonatal morbidity, with the f
204  primary outcome was a composite of fetal or neonatal death or the need for placement of a cerebrospi
205 ere subfertile with small litters and higher neonatal death (P < 0.02).
206 ficantly lower in the intervention arm (21.3 neonatal deaths per 1000 live births vs 30.1 per 1000 in
207 elated inequality increased by more than 1.5 neonatal deaths per 1000 livebirths per year in Ethiopia
208 th distribution was reduced by more than two neonatal deaths per 1000 livebirths per year.
209 s per 1000 total births, and no more than 10 neonatal deaths per 1000 livebirths, compatible with the
210 eaths per 1000 pregnancies and 2.4 (0.7-4.1) neonatal deaths per 1000 livebirths.
211 eaths per 1000 pregnancies and 2.3 (0.9-3.7) neonatal deaths per 1000 livebirths.
212 0,396 deaths) to estimate the proportions of neonatal deaths per day and used bootstrap sampling to d
213                                              Neonatal death, preterm birth, and pregnancy loss occurr
214 ficient for rescuing Insr knockout mice from neonatal death, preventing diabetes ketoacidosis, and no
215  rescues insulin receptor knockout mice from neonatal death, prevents diabetes in a majority of anima
216                       Consequently, a higher neonatal death rate (57.1%) in hUGT1/Tlr2(-/-) mice was
217 ed in respiratory dysfunction and invariable neonatal death, related to the complete absence of matur
218 762-163 513 and 279 584-803 129 maternal and neonatal deaths, respectively.
219 chanical ventilation >/=24 h, stillbirth, or neonatal death); respiratory distress syndrome; any mech
220         Among the live births, there were 59 neonatal deaths, seven postneonatal deaths (first 28 day
221 s the rate of a composite primary outcome of neonatal death, severe intraventricular haemorrhage (IVH
222                      National aims to reduce neonatal deaths should be set, and interventions incorpo
223 interval (CI): 1.38, 1.54 (n = 57 studies)), neonatal death (sRR = 1.22, 95% CI: 1.14, 1.30 (n = 28))
224 e disease in ruminants, in which it leads to neonatal death, the human disease phenotype is generally
225 ristics associated with an increased risk of neonatal death, the rate was lower in the regions with 4
226     In 2010, due to a pertussis outbreak and neonatal deaths, the California Department of Health rec
227 goal of reducing the numbers of maternal and neonatal deaths, the Government of India launched Janani
228 ficantly increased the risk of stillbirth or neonatal death (three [4%] of 69, 4.7 [1.2-19.0]).
229 erity of renal disease, which can range from neonatal death to adequate function into old age, charac
230                      Adverse events included neonatal death (two in the standard care group and three
231  death, defined as intrapartum stillbirth or neonatal death unrelated to congenital anomaly, compared
232 d related these to the risk of stillbirth or neonatal death using Poisson regression analysis.
233                    The risk of stillbirth or neonatal death was 1.7% versus 0.7% (odds ratio, 2.39; 9
234                           The odds ratio for neonatal death was 2.81 (95% CI: 0.73, 10.8).
235                                  The rate of neonatal death was similar between groups (2.54 vs 2.21
236 adiation and malformations, stillbirths, and neonatal deaths was not seen in the children of female s
237                    The corresponding ORs for neonatal death were 0.89 (95% CI, 0.58-1.39; P = .62) fo
238 ate that 3900 early-onset infections and 200 neonatal deaths were prevented in 1998 by the use of int
239 hs, 5,470 cases of low birth weight, and 430 neonatal deaths were prevented.
240                                          482 neonatal deaths were recorded.
241                      Combined fetal loss and neonatal deaths were reduced by 11% (RR 0.89, 0.81-1.00,
242 mutations resulted in severe phenotypes with neonatal death, whereas missense changes resulted in imp
243  and palate (one), microtia alone (one), and neonatal death with multiple malformations (one).
244     Sepsis is the third most common cause of neonatal death, with Group B Streptococcus (GBS) being t
245 weeks' gestation, are at the highest risk of neonatal death, with ongoing post-neonatal mortality ris
246 s that generated funds for transport reduced neonatal deaths, with the largest effect seen in India (
247 ster MRI exposure, the risk of stillbirth or neonatal death within 28 days of birth and any congenita
248 an section, Apgar score <7 at 5 minutes, and neonatal death within 28 days.
249  or mechanical ventilation) or stillbirth or neonatal death within 72 hours after delivery.
250    Preterm birth (PTB) is a leading cause of neonatal death worldwide.
251                       The 2.9 million annual neonatal deaths worldwide are attributable to three main
252            While information about 4 million neonatal deaths worldwide is limited, even less informat
253 rventions could avert an estimated 41-72% of neonatal deaths worldwide.
254 bor and infections are the leading causes of neonatal deaths worldwide.
255  infections remain one of the main causes of neonatal deaths worldwide.

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