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1 of other morbid conditions in full-term and very low birth weight infants.
2 sk factor for intraventricular hemorrhage in very low birth weight infants.
3 y protein intake may improve growth in these very low birth weight infants.
4 and aggressive administration of protein to very low birth weight infants.
5 al palsy in a geographically based cohort of very low birth weight infants.
6 easure clinical risk and illness severity in very low birth-weight infants.
7 such facilities might reduce mortality among very-low-birth-weight infants.
8 ious levels of care and different volumes of very-low-birth-weight infants.
9 gulase-negative staphylococcal infections in very-low-birth-weight infants.
10 ncommon but potentially lethal problem among very-low-birth-weight infants.
11 rcent of low-birth-weight and 4.3 percent of very-low-birth-weight infants.
12 our weeks of age in 371 ventilator-dependent very-low-birth-weight infants (501 to 1500 g) who had re
15 liver disease, necrotizing enterocolitis in very low birth weight infants, and hepatic encephalopath
17 dysplasia (BPD) is a chronic lung disease of very low birth weight infants, associated with oxygen th
18 r, double-blind randomized clinical trial in very low-birth-weight infants (birth weight <1500 g) adm
19 ree days of life and compared them with 7606 very-low-birth-weight infants born at centers in the net
20 We compared a cohort of 242 survivors among very-low-birth-weight infants born between 1977 and 1979
22 among black infants, the mortality rate for very-low-birth-weight infants did not change significant
23 eding support by nurses have higher rates of very low birth weight infants discharged home on human m
24 evel between the dependent variable (rate of very low birth weight infants discharged on "any human m
25 e nature of dermal structure and function in very low birth weight infants, evidence of mechanical fr
27 occurring within 72 hours after birth) among very-low-birth-weight infants have changed in recent yea
29 possible after birth at 2.5-3.0 g/kg/day in very low birth weight infants; however, there are no lon
30 proportionate number of low-birth-weight and very-low-birth-weight infants in the United States, in p
34 (2500-3999 g), while the admission rate for very low-birth-weight infants (<1500 g) was 844.1 per 10
35 th a high level of care and a high volume of very-low-birth-weight infants (more than 100 per year),
38 oid (GC) therapy, while approximately 19% of very low birth weight infants receive postnatal GC thera
39 e risk of necrotizing enterocolitis (NEC) in very low birth weight infants receiving indomethacin (IN
40 life yielded similar short-term outcomes in very low-birth-weight infants regarding safety and effic
41 ctice did not improve outcomes in premature, very low-birth-weight infants requiring a transfusion.
42 cently provided reference range for uNGAL in very low birth weight infants shows that normative value
48 assess neonatal mortality rates among 48,237 very-low-birth-weight infants who were born in Californi
49 compassionate use of tin mesoporphyrin in a very low birth weight infant with intrauterine growth re
50 exists regarding the best method of managing very low birth weight infants with PDA and whether to em
51 Prevention of IC has become a major focus in very low birth weight infants, with fluconazole increasi
52 lation in terms of the pulmonary outcome for very-low-birth-weight infants without an increase in the
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