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1 tant implications in the clinical setting of chronic renal insufficiency.
2 processes and is a major cause of acute and chronic renal insufficiency.
3 the clinical and public health importance of chronic renal insufficiency.
4 ter contrast administration in patients with chronic renal insufficiency.
5 sed along with the changes that occur during chronic renal insufficiency.
6 ze in patients with renovascular disease and chronic renal insufficiency.
7 ts with obstructive renovascular disease and chronic renal insufficiency.
8 of the renal CaSR is altered in experimental chronic renal insufficiency.
9 etes mellitus (45.5% versus 30.8%; P<0.001), chronic renal insufficiency (19.2% versus 10.7%; P<0.001
10 hypertension (77% versus 65%; P=0.006), and chronic renal insufficiency (34% versus 19%; P<0.0001).
13 h terms including "chronic kidney disease", "chronic renal insufficiency", "albuminuria", "proteinuri
14 cline in renal function of patients who have chronic renal insufficiency, although these agents do no
16 dy mass index, 36 kg/m(2)), stage 3 vascular chronic renal insufficiency, and hebephrenic schizophren
17 sity (body mass index, 36), stage 3 vascular chronic renal insufficiency, and hebephrenic schizophren
18 ients with decompensated heart failure, mild chronic renal insufficiency, and renal function that had
19 endovascular repair (EVAR) in patients with chronic renal insufficiency because of the concern that
20 ma proteins among 1067 participants from the Chronic Renal Insufficiency Cohort (CRIC) and 536 indivi
21 oth time periods in 3249 participants in the Chronic Renal Insufficiency Cohort (CRIC) and 703 partic
22 nts with predialysis CKD using data from the Chronic Renal Insufficiency Cohort (CRIC) and CKD Japan
23 l analysis of participants enrolled into the Chronic Renal Insufficiency Cohort (CRIC) and Hispanic-C
24 participants undergoing hemodialysis in the Chronic Renal Insufficiency Cohort (CRIC) and Predictors
26 Disease and Hypertension (AASK, n =703), the Chronic Renal Insufficiency Cohort (CRIC) study ( n =319
27 ease in Children (CKiD) cohort II ( n =248), Chronic Renal Insufficiency Cohort (CRIC) study ( n =337
28 Data from 3,939 participants enrolled in the Chronic Renal Insufficiency Cohort (CRIC) Study between
29 ers in the United States who enrolled in the Chronic Renal Insufficiency Cohort (CRIC) Study between
31 AKI (ASSESS-AKI) study and the subset of the Chronic Renal Insufficiency Cohort (CRIC) study enrollee
33 tion and quality with CKD progression in 431 Chronic Renal Insufficiency Cohort (CRIC) Study particip
35 ysis, we studied 3483 people with CKD in the Chronic Renal Insufficiency Cohort (CRIC) Study recruite
36 s among 2696 participants in the prospective Chronic Renal Insufficiency Cohort (CRIC) study to ident
38 d HF among 3093 participants enrolled in the Chronic Renal Insufficiency Cohort (CRIC) Study who did
39 ine from participants with diabetes from the Chronic Renal Insufficiency Cohort (CRIC) study, the Sin
40 7) selected for metabolomic profiling in the Chronic Renal Insufficiency Cohort (CRIC) study, the sta
41 Using a subset of 1214 participants in the Chronic Renal Insufficiency Cohort (CRIC) Study, we dete
44 WAS of 537 blood metabolites measured in the Chronic Renal Insufficiency Cohort (CRIC) Study, with se
50 ns) was analysed in 2906 participants of the Chronic Renal Insufficiency Cohort (CRIC) with validatio
51 redictors of incident hospitalized HF in the Chronic Renal Insufficiency Cohort (CRIC), a multiethnic
54 rom the Cure Glomerulopathy Network and 3939 Chronic Renal Insufficiency Cohort adult participants.
55 n and African ancestry participants from the Chronic Renal Insufficiency Cohort and Atherosclerosis R
56 sease stages 2 through 4 who enrolled in the Chronic Renal Insufficiency Cohort between June 2003 and
57 n analysis in 500 subjects with DKD from the Chronic Renal Insufficiency Cohort for DKD phenotypes, i
59 tamin K status is low, were measured in 3066 Chronic Renal Insufficiency Cohort participants (median
60 eparation by CKD-EPI estimating equations in Chronic Renal Insufficiency Cohort participants, on the
63 of 4091 proteins and 630 metabolites in the Chronic Renal Insufficiency Cohort study (N=1708; averag
64 cations in the United States enrolled in the Chronic Renal Insufficiency Cohort Study and followed up
65 with mild to severe CKD who enrolled in the Chronic Renal Insufficiency Cohort Study between June 19
68 a subset of 942 participants with CKD in the Chronic Renal Insufficiency Cohort Study who had at leas
70 asma proteins among 3235 participants of the Chronic Renal Insufficiency Cohort Study with the primar
71 ts (1778 women and 2161 men) enrolled in the Chronic Renal Insufficiency Cohort Study, a large, diver
74 pective analysis of 3747 participants in the Chronic Renal Insufficiency Cohort Study, we investigate
83 olymorphisms [SNPs]) of CAC within the CRIC (Chronic Renal Insufficiency Cohort) study (N = 1,509; 57
85 th chronic kidney disease in the CRIC study (Chronic Renal Insufficiency Cohort) who were free of HF
86 prospective cohort study used data from the Chronic Renal Insufficiency Cohort, a multicenter cohort
87 rogression in four CKD cohorts (N=5654): the Chronic Renal Insufficiency Cohort, the African American
88 In a prospective case-cohort study of the Chronic Renal Insufficiency Cohort, we measured FGF23 at
93 nt deployment was performed in patients with chronic renal insufficiency (creatinine >1.5 mg. dL(-1))
94 his is caused by the increased prevalence of chronic renal insufficiency (CRI) among blacks or by the
95 mance, and LV contractility in children with chronic renal insufficiency (CRI) and children undergoin
96 ease and total mortality among patients with chronic renal insufficiency (CRI) and end-stage renal di
97 ody mass are commonly found in patients with chronic renal insufficiency (CRI) and especially in dial
98 but less is known about the epidemiology of chronic renal insufficiency (CRI) and its relationship t
99 tion develop at the time of mild to moderate chronic renal insufficiency (CRI) and progress as renal
100 Comorbid conditions that develop during chronic renal insufficiency (CRI) contribute to the high
101 sive growth retardation is a complication of chronic renal insufficiency (CRI) in children and often
106 t there are few studies of iron status among chronic renal insufficiency (CRI) subjects not yet requi
107 owever, SHPT begins during earlier stages of chronic renal insufficiency (CRI), and little is known a
108 nd (2) to compare health of patients who had chronic renal insufficiency (CRI), were on dialysis, and
109 nty-four children were treated with polyuric chronic renal insufficiency (CRI; creatinine clearance <
110 n incident ESRD outpaced growth in prevalent chronic renal insufficiency, demonstrating that the ESRD
111 , cardiomegaly, peripheral vascular disease, chronic renal insufficiency, diabetes mellitus, low body
113 , 2.2 [CI, 1.5 to 3.3]; P < 0.001), and mild chronic renal insufficiency (hazard ratio, 2.4 [CI, 1.7
116 eveloped in 1983, but every 1000 adults with chronic renal insufficiency in 1991 produced 16 new case
117 the number of adults age 20 to 74 years with chronic renal insufficiency increased from 2.6 to 3.9 mi
121 ted with CAD score were age, hyperlipidemia, chronic renal insufficiency, left ventricular function,
122 11 million people in the United States have chronic renal insufficiency, little is known about ethni
123 uggest that reduced renal CaSR expression in chronic renal insufficiency may play a role in disordere
124 The remaining 17 patients all have developed chronic renal insufficiency (mean serum creatinine, 2.4
128 who smoked less than 5 cigarettes/day, with chronic renal insufficiency or prior cancer, were exclud
129 ge, sex, baseline blood pressure, history of chronic renal insufficiency, presence of diabetes mellit
132 ntified in plasma samples from patients with chronic renal insufficiency were also found in the plasm
134 tion in patients with glomerular disease and chronic renal insufficiency, which might inhibit or pote