ライフサイエンスコーパス: full-term infant

1 lation between abuse and low birth weight in full term infants.

2 that differentiate them from sham stimuli in full-term infants.

3 value was high despite a low recall rate in full-term infants.

4 (< 2,500 g), and birth weight (grams) among full-term infants.

5 ociation between PFOS and birth weight among full-term infants.

6 tion may adversely affect birth weight among full-term infants.

7 as issues pertaining to feeding preterm and full-term infants.

8 m the umbilical cord veins of their healthy, full-term infants.

9 yse associated factors in former preterm and full-term infants.

10 d cerebral palsy or cPVL in both preterm and full-term infants.

11 n in RA women after disease onset) and small full-term infants.

12 compared with results from our database for full-term infants.

13 t formula affects the iron status of healthy full-term infants.

14 ity of poor cognitive outcomes compared with full-term infants.

15 The recall rate in full-term infants (0.03%) was lower than that in preterm

16 Overall, 4/264 (2%) full-term infants, 15/125 (12%) preterm-infants with GA

17 association between PFOS and birth weight in full-term infants (-29 g per log unit increase; 95% CI:

18 Among 125 singleton full-term infants, 4 (3.2%) had low birth weights.

19 (mean +/- SD, 26.1 +/- 13.8%) compared with full-term infants (7.3 +/- 8.2%; P = 0.020) and prematur

20 Among full-term infants, a positive association was found betw

21 40 full-term infants aged 6 months and younger were given v

22 ed in a forward-masking paradigm in healthy, full-term infants aged 6 weeks (n = 111) and 9 months (n

23 Eighteen full-term infants (aged 8-12 wk at enrollment) were fed

24 The authors recorded VEPs from 57 healthy full-term infants and 4 adults.

25 ity of handheld SD OCT imaging of the ONH in full-term infants and children without anaesthesia or se

26 erate the number of T cells was performed on full-term infants and preterm infants when they reached

27 microbiome colonization patterns relative to full-term infants, and it is speculated that the hospita

28 of birth is recognised in about one in 4000 full-term infants, and may present with neurological and

29 Randomized clinical trial of 382 full-term infants born after a low-risk pregnancy at a S

30 included in the original study (n = 382) as full-term infants born after a low-risk pregnancy were i

31 A total of 145,456 singleton full-term infants born alive and whose mothers were cove

32 A total of 14,189 full-term infants born in the United Kingdom on April 5

33 The results of this study suggest that for full-term infants, breast-feeding is associated with enh

34 nt risk factors for low birth weight for the full term infants but not the preterm infants on a bivar

35 t infants and 534 were non-low-birth-weight, full-term infants (control).

36 6-week-old full-term infants due for their first polio vaccinations

37 received non-selenium-fortified preterm and full-term infant formulas containing 0.12 and 0.11 mumol

38 2 g) received selenate-fortified preterm and full-term infant formulas containing 0.36 and 0.22 mumol

39 Full-term infants from 2 to 4 months of age and pre-pres

40 eterm infant (preterm women), or delivered a full-term infant (full-term women).

41 Some healthy full-term infants have bilateral subfoveal fluid not obv

42 why disease severity differs among healthy, full-term infants; however, virus titers, inflammation,

43 ping of the umbilical cord of normal-weight, full-term infants improved iron and haematological statu

44 lies in Honduras, 3) low-birth-weight (LBW), full-term infants in Honduras, and 4) infants in Ghana.

45 The probability of low birth weight among full-term infants in the population was estimated using

46 -fovea distance were measured in preterm and full-term infants in vivo.

47 Compared with full-term infants, lymphocytes from preterm infants had

48 e dramatically different from those in which full-term infants mature and thus likely impact the deve

49 ne, p < 0.05) than did children who had been full-term infants of normal birthweight.

50 ood T lymphocytes from preterm compared with full-term infants (P = 0.008).

51 ency of miscarriage, premature births, small full-term infants, perinatal deaths, and births of live

52 Full-term infants show a decline in their discrimination

53 ent RNFL thickness measurements for healthy, full-term infants that may serve as normative data for f

54 children who had been normal birthweight and full-term infants, the cromolyn without steroids group h

55 Fifty full-term infants were adequately imaged for RNFL analys

56 e milk of mothers giving birth to preterm or full-term infants were not significantly different.

57 wever, adequate to meet the calcium needs of full-term infants when the formula's calcium content is

58 cits of cerebral palsy (CP) in premature and full-term infants who present with neonatal encephalopat

59 In a prospective, multicenter study, 58 full-term infants with severe hypoxemia and persistent p

60 nd feasibility phase 1/2 trial, we recruited full-term infants younger than 48 h who had hypoxic isch

61 brile (>/=38 degrees C), previously healthy, full-term infants younger than 60 days for whom blood cu