ライフサイエンスコーパス: urine collection

1 randomly selected to participate in the 24-h urine collection.

2 generally greater with PCP use within 6 h of urine collection.

3 ng; external counting; and blood, fecal, and urine collection.

4 cretion rate should be measured from a timed urine collection.

5 is most precisely ascertained by using timed urine collection.

6 nction in animal studies that do not involve urine collection.

7 residence at cohort enrollment, and date of urine collection.

8 external probe and calibrated using complete urine collections.

9 ing, plasma clearance measurements and timed urine collections.

10 markers of dietary protein in their 24-hour urine collections.

11 ations, but few large-scale studies use 24-h urine collections.

12 akes estimated from 24-h dietary recalls and urine collections.

13 from four 24-h dietary recalls and two 24-h urine collections.

14 iltration rate, and proteinuria from 24-hour urine collections.

15 um excretion was measured in 2 baseline 24-h urine collections.

16 ulation-based study including data from 24-h urine collections.

17 d four 24-h dietary recalls and 2 timed 24-h urine collections.

18 um excretion was measured daily in the 24-hr urine collections.

19 ith coronary artery disease provided 24-hour urine collections.

20 24-hour dietary recalls and 2 timed 24-hour urine collections.

21 tion and metabolism were assessed using 24-h urine collections.

22 lipid peroxidation, was measured in 24 hour urine collections.

23 CEHC and alpha-CMBHC excretions in three 8-h urine collections (0-24 h) and plasma alpha-tocopherol,

24 in a diverse urban population by using 24-h urine collections, 2) corroborate potassium excretion by

25 Two overnight urine collections (48 h apart) from 170 uterine fibroid

26 212 persons [75% of those selected for 24-h urine collection; 53% (equal to 71% x 75% of those selec

27 s, an oral glucose tolerance test, overnight urine collection, a 12-lead resting electrocardiogram, m

28 Among those with a complete 24-h urine collection, a random one-half were asked to collec

29 dardized 24-hour dietary recalls and 24-hour urine collections administered over 3 years of follow-up

30 ribution was assumed in the body organs with urine collection after the study.

31 diagnosed with incident breast cancer after urine collection and before June 1, 2007.

32 g status, menopausal status, or time between urine collection and diagnosis (all Pinteraction values

33 t cancer among women with </=5 years between urine collection and diagnosis was 0.74 (Q4 vs. Q1; 95%

34 aminants might leach from materials used for urine collection and influence statistical analysis of m

35 ne albumin and creatinine in an untimed spot urine collection and reporting albumin-to-creatinine rat

36 of renal dysfunction over the 72 hours after urine collection and with hospital mortality.

37 Twenty-four-hour urine collections and 24-h ambulatory blood pressure ass

38 NO metabolites (NOx) were assayed in 24-hour urine collections and exhaled NO (FE(NO)) determined at

39 At the end of each period, 24-h urine collections and fasting blood samples were obtaine

40 Serial blood samples, 24-hr urine collections and nuclear images were collected unti

41 Serial blood samples, 24-hr urine collections and nuclear images were collected up t

42 ult equation, creatinine clearance from 24-h urine collection, and a new regression equation derived

43 Baseline fasting blood, overnight urine collection, and clinical measurements were perform

44 Renal function was assessed by 24-h urine collection, and CRI was defined as measured creati

45 one matched (age, menopausal status, date of urine collection, and day of laboratory assay) to popula

46 a medical history and physical examination, urine collection, and phlebotomy.

47 Data included blood and urine collections, and the organ uptake value was measur

48 ssessed the feasibility of implementing 24-h urine collections as part of a nationally representative

49 Sodium excretion was measured in two 24-hour urine collections at baseline.

50 Potassium was measured in 24-h urine collections at baseline.

51 hout proteinuria (20 mg protein in a 24-hour urine collection) at 30(6)/(7) weeks of gestation.

52 rea excretion was measured in repeated 24-hr urine collections between 6 and 18 months after transpla

53 sirable in the areas of anesthesia, ureteral urine collections, blood collections, volume replacement

54 ly, these have been quantified using a 24-hr urine collection, but spot urine measurements (albumin-c

55 erage sodium excretion from multiple 24-hour urine collections, but such an approach is impractical.

56 A single 24-h urine collection cannot predict sodium, potassium, or ch

57 lytes is difficult and usually predicated on urine collections, commonly for 24 h, which are consider

58 intigraphy was 58.3 +/- 4.7 h (n = 20), with urine collection confirming the loss of between 2.2% and

59 bset of 10 PCPs that were used within 6 h of urine collection contributed to at least 70% of the weig

60 This suggests that fasting blood and urine collections could be used to estimate polyphenol b

61 ard for estimating sodium intake is the 24-h urine collection, few studies have used this biomarker t

62 ntion trials can be determined with a single urine collection for albuminuria assessment per study vi

63 ded a fasting blood sample and a single 24-h urine collection for stone risk analysis.

64 ation of all cases, the utility of a 24-hour urine collection for uric acid, and even the difficulty

65 stimation supports the continued use of 24-h urine collections for assessing population and individua

66 ial donors performed one to three outpatient urine collections for Ccr measurement.

67 low-burden, low-cost alternative to 24-hour urine collections for estimation of population sodium in

68 ) and remained significantly elevated in all urine collections for the 8-h period of the study (analy

69 However, urine collection from newborn infants presents a potenti

70 They obtained 24-hour urine collections from 121 consecutive clinic patients w

71 e electrophoresis of a sample from a 24-hour urine collection (grade A).

72 explicit instructions, started and ended the urine collection in a urine study mobile examination cen

73 We were able to test the value of 24-h urine collections in a unique, ultra-long-term balance s

74 ars with complete blood pressure and 24-hour urine collections in the 2014 National Health and Nutrit

75 ) years after gadolinium exposure, a 24-hour urine collection indicated that the gadolinium level rem

76 In this paper, a novel approach for urine collection is proposed, which circumvents many of

77 nalyses that excluded potentially incomplete urine collections [Mage's equation mean difference: -109

78 as to identify and recommend the appropriate urine collection method for the study of bacterial commu

79 nary metabolites of F2-isoprostanes in timed urine collections offers an advantage over measuring unm

80 s determined from isotope enrichment in spot urine collections on days 3-7.

81 en were exposed to all phthalates during the urine collection periods.

82 d water protocol (energy biomarker), 24-hour urine collection (protein biomarker), and self-reports o

83 insurmountable, logistic challenges of 24-h urine collection remain a barrier for research on the re

84 by a radionuclide method not dependent upon urine collection (rGFR).

85 was documented (780 mg protein in a 24-hour urine collection), schistocytes were detected in the per

86 creatinine ratio in this population, a 24-hr urine collection should be considered before making majo

87 nd demonstrated that their use within 6 h of urine collection strongly predicted MEP and paraben urin

88 ma and PTSD, was used to select a subset for urine collection studies conducted in a sleep laboratory

89 l voiding patterns, acute urinary retention, urine collection techniques, diagnosis in young infants,

90 subset of participants who completed a 24-h urine collection, the risk for kidney stones was directl

91 TS immunoglobulin (Ig)G, followed by an 18-h urine collection to quantitate the excretion of albumin

92 which takes an average of 1.5 to 2 days from urine collection to results, delaying optimal therapy.

93 report Bland-Altman analyses on the value of urine collections to estimate intake.

94 nts using meticulously obtained timed 6-hour urine collections to quantify loop diuretic-induced cumu

95 ght fast; no other foods were ingested until urine collection was complete.

96 A 24-hr urine collection was obtained for determination of [15N]

97 A 24-h urine collection was obtained simultaneously.

98 A 24-hour urine collection was performed on days 17 and 29 postinj

99 tions, and an aliquot of the preceding 6 hrs urine collection was sent for magnesium and potassium de

100 . 1.73 m(-2) The mean +/- SD number of 24-h urine collections was 3.5 +/- 0.8/participant, and the m

101 ted seafood consumption within 2 days before urine collection were excluded from the analyses.

102 ls (0-6 and 7-24 h), and aliquots from these urine collections were analyzed using high performance l

103 Baseline urine aliquots and 24-hr urine collections were collected on days 3, 7, and 11 du

104 um concentration, 3-d food records, and 24-h urine collections were completed at baseline and 4 wk.

105 response rate and 75% completion rate, 24-h urine collections were deemed feasible and implemented i

106 taining known amounts of MeIQx and PhIP, and urine collections were made 0-12 and 12-24 h after a mea

107 od pressure monitoring was done and complete urine collections were made for the next 36 h.

108 Two consecutive 24-h urine collections were obtained after a baseline period

109 In 2013, 24-hour urine collections were obtained from 554 participants in

110 mated to metabolism cages, and baseline 24-h urine collections were obtained.

111 Plasma sampling and urine collections were performed on both days 1 and 5 of

112 Plasma sampling and urine collections were performed to characterize the pha

113 daily blood samples were obtained and 24-hr urine collections were performed.

114 bumin (0.25 MBq), multiple blood samples and urine collections were taken between 0 and 4 h.

115 Ten-hour overnight urine collections were taken for measurement of urinary

116 inary albumin-to-creatinine ratio (ACR; spot urine collection) were measured in 5042 participants in

117 Urine collection within 15 mins of intensive care unit a