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1 otor impairment in 11-year-old children with very low birth weight.
2 d more for white than for black infants with very low birth weights.
3 of nosocomial infections among infants with very low birth weights.
4 % vs 5.6%), low birth weight (9.4% vs 9.0%), very low birth weight (1.6% vs 1.5%), and death in the f
6 istics information for all 1563 infants with very low birth weights (500 to 1500 g) born from 1987 th
8 dults who were born very preterm and/or with very low birth weight and 106 term-born control subjects
10 tive risk of death among black newborns with very low birth weights as compared with white newborns w
11 ease inhibitors (5 percent) had infants with very low birth weight, as compared with nine women who r
13 eased 17 percent, from 220.3 deaths per 1000 very-low-birth-weight babies born alive (in 1987 through
14 ces in neonatal mortality among infants with very low birth weight (below 1500 g) among NICUs with va
15 The childhood respiratory consequences of very low birth weight (birth weight < or =1,500 g) are i
16 dults who were born very preterm and/or with very low birth weight, cBF volumes were significantly re
17 hors followed to age 8 years a cohort of 384 very low birth weight children from six regional neonata
21 el of care and had a high volume, but 92% of very-low-birth-weight deliveries occurred in urban areas
22 .4, 3.1), respectively; the relative risk of very low birth weight for infants with US-born Black mot
23 the mortality rate among white newborns with very low birth weights (from 261.5 per 1000 to 155.5 per
28 compassionate use of tin mesoporphyrin in a very low birth weight infant with intrauterine growth re
32 eding support by nurses have higher rates of very low birth weight infants discharged home on human m
33 evel between the dependent variable (rate of very low birth weight infants discharged on "any human m
35 oid (GC) therapy, while approximately 19% of very low birth weight infants receive postnatal GC thera
36 e risk of necrotizing enterocolitis (NEC) in very low birth weight infants receiving indomethacin (IN
37 cently provided reference range for uNGAL in very low birth weight infants shows that normative value
39 exists regarding the best method of managing very low birth weight infants with PDA and whether to em
41 liver disease, necrotizing enterocolitis in very low birth weight infants, and hepatic encephalopath
42 dysplasia (BPD) is a chronic lung disease of very low birth weight infants, associated with oxygen th
43 e nature of dermal structure and function in very low birth weight infants, evidence of mechanical fr
44 Prevention of IC has become a major focus in very low birth weight infants, with fluconazole increasi
50 possible after birth at 2.5-3.0 g/kg/day in very low birth weight infants; however, there are no lon
52 (2500-3999 g), while the admission rate for very low-birth-weight infants (<1500 g) was 844.1 per 10
53 r, double-blind randomized clinical trial in very low-birth-weight infants (birth weight <1500 g) adm
56 life yielded similar short-term outcomes in very low-birth-weight infants regarding safety and effic
57 ctice did not improve outcomes in premature, very low-birth-weight infants requiring a transfusion.
58 our weeks of age in 371 ventilator-dependent very-low-birth-weight infants (501 to 1500 g) who had re
59 th a high level of care and a high volume of very-low-birth-weight infants (more than 100 per year),
62 ree days of life and compared them with 7606 very-low-birth-weight infants born at centers in the net
63 We compared a cohort of 242 survivors among very-low-birth-weight infants born between 1977 and 1979
65 among black infants, the mortality rate for very-low-birth-weight infants did not change significant
66 occurring within 72 hours after birth) among very-low-birth-weight infants have changed in recent yea
68 proportionate number of low-birth-weight and very-low-birth-weight infants in the United States, in p
71 assess neonatal mortality rates among 48,237 very-low-birth-weight infants who were born in Californi
72 lation in terms of the pulmonary outcome for very-low-birth-weight infants without an increase in the
79 and oligodendrocytes, in preterm babies with very low birth weight is associated with decreased cereb
83 tion of the low-birth-weight babies having a very low birth weight (<1,500 g) in the more recent birt
84 birth weight (less-than-or-equal 2500 g) and very low birth weight (<1500 g) among infants conceived
85 infants born to both groups; and the rate of very low birth weight (<1500 g) was 2 percent for the gr
87 on 422 duodenal aspirates collected from 122 very-low-birth-weight (<1,500-g) newborns, at the time o
92 mo corrected age for a historical cohort of very-low-birth-weight neonates (<1250 g) who were admitt
97 A multicentered clinical trial found that very low-birth weight preterm infants given bovine lacto
98 double-blind, randomized controlled study of very-low-birth-weight preterm neonates randomly allocate
103 ; 95% confidence interval [CI], 1.3-2.3) and very low birth weight (RR, 1.9; 95% CI, 1.3-2.7) than wi
104 Heavy growth of E. coli had a higher risk of very low birth weight than light growth (RR, 2.4; 95% CI
106 ded particulates (TSP) and risk for having a very low birth weight (VLBW) baby, i.e., one weighing le
111 ving infants born very preterm (VPT) or with very low birth weight (VLBW) is necessary to guide clini
115 eton birth categories: 450 fetal deaths; 782 very low birth weight (VLBW, < 1,500 g); 802 moderately
116 extremely low birth weight (ELBW, <1000 g), very low birth weight (VLBW, 1000-1499 g), moderately lo
117 or morphometric analysis was performed on 50 very low birth weight (VLBW, birth weight </=1500 g), 49
118 The authors examined the relation between very low birth weight (VLBW: < 1,500 g) and possible dev
119 olitis represent a high-risk subgroup of the very low-birth-weight (VLBW) (<1500 g) population that w
122 end of antibiotic use among all hospitalized very low-birth-weight (VLBW) infants across Canada and t
123 inatal regionalization have recommended that very low-birth-weight (VLBW) infants be born at highly s
124 ) is typically benign in term infants but in very low-birth-weight (VLBW) infants can cause pneumonit
130 rt study from January 2010 to February 2014, very low-birth-weight (VLBW, </=1500 g) infants, within
131 ent how parents adapt to the experience of a very low-birth-weight (VLBW; <1500 g) birth despite soci
133 f initiation of parenteral lipid infusion to very-low-birth-weight (VLBW) infants varies widely among
136 irth weight ([LBW] 1.8 to 2.24 kg) and three very low birth weight ([VLBW] < or = 1.36 kg) infants, f
137 fections are commonly present in preterm and very low-birth-weight (VLWB) infants and might contribut
138 dults who were born very preterm and/or with very low birth weight was specifically associated with b
139 survival without disability in children with very low birth weights who were assessed at 5 years.
140 mounting to a sevenfold reduction in risk of very low birth weight with first trimester supplementati
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