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1 nol equivalent (200,000 IU), on HIV load and CD4 lymphocyte count.
2 lated with RNA copy number (P < .01) but not CD4 lymphocyte count.
3 of KSHV/HHV-8 DNA did not correlate with the CD4 lymphocyte count.
4 county, age group, sex, HIV/AIDS status, and CD4 lymphocyte count.
5 rifamycin resistance among patients with low CD4 lymphocyte counts.
6 al reasons may account for BL deficit at low CD4 lymphocyte counts.
7 ith ongoing HIV replication but may increase CD4+ lymphocyte counts.
8 infection and inversely correlates with the CD4(+) lymphocyte count.
9 correlated with lower viral loads and higher CD4(+) lymphocyte counts.
10 gly associated with HIV RNA levels than with CD4(+) lymphocyte counts.
11 red immunodeficiency syndrome (AIDS) (median CD4+ lymphocyte count -21/microl) who participated in a
12 of control subjects (odds ratio adjusted for CD4 lymphocyte count, 3.8; 95% confidence interval, 2.2-
13 f the 494 study participants (median initial CD4(+) lymphocyte count, 518 lymphocytes/mm(3)), 90 (18%
14 The HIV test result was negative, and the CD4 lymphocyte count and complement and immunoglobulin l
19 n ongoing hepatitis C virus (HCV) infection, CD4 lymphocyte counts and serum concentrations of HCV RN
23 te, these effects remained significant after CD4+ lymphocyte count and plasma HIV-1 RNA load at basel
24 t HIV-1 disease progression independently of CD4+ lymphocyte count and plasma HIV-1 RNA load, suggest
25 ad strongly predicts the rate of decrease in CD4+ lymphocyte count and progression to AIDS and death,
26 ollowed (in order of predictive strength) by CD4+ lymphocyte count and serum neopterin levels, serum
27 th past or current HGV infection have higher CD4+ lymphocyte counts and better AIDS-free survival rat
28 oth men and women, is associated with higher CD4+ lymphocyte counts and lower plasma HIV viral burden
30 by the use of end points such as changes in CD4+ lymphocyte counts and plasma levels of human immuno
31 ral load discriminated risk at all levels of CD4+ lymphocyte counts and predicted their subsequent ra
34 or type II (sTNF alpha RII) levels in serum, CD4 lymphocyte counts, and human immunodeficiency virus
35 ed clinical, demographic, and exposure data, CD4 lymphocyte counts, and stool samples for detection o
36 younger, injection drug use, lower baseline CD4+ lymphocyte count, and higher baseline viral load.
39 Two key laboratory markers--plasma RNA and CD4+ lymphocyte count-are independent predictors of clin
40 ciated with the magnitude of the increase in CD4 lymphocyte count, as were haplotypes in genes encodi
41 ion had no significant impact on HIV load or CD4 lymphocyte count at 2 and 4 weeks after treatment.
44 he same CD4 count, whereas women have higher CD4 lymphocyte counts at the time of AIDS diagnosis.
45 , a higher weight, and HIV viremia and lower CD4 lymphocyte counts at the time of HAV vaccination wer
46 se at 6 months of HAV vaccination and higher CD4 lymphocyte counts at vaccination were inversely asso
49 increased with early infection, low maternal CD4+ lymphocyte count at recruitment, and frequent morbi
50 th each of the following: decreased maternal CD4+ lymphocyte counts at base line; decreased maternal
52 lure or relapse was associated with baseline CD4 lymphocyte count, being 12.3% (9/73; 95% confidence
53 other non-Hodgkin lymphoma (NHL), by age and CD4 lymphocyte count categories, were estimated using Po
54 RNA level plus a 10 percent increase in the CD4+ lymphocyte count could explain 79 percent of the tr
55 22 who were positive for HGV RNA, had higher CD4+ lymphocyte counts (difference, 211 cells/mm3 [95% C
57 medical histories, serum HIV RNA loads, and CD4+ lymphocyte counts for mothers were examined by logi
58 eatment-naive or interferon-experienced, had CD4+ lymphocyte count >/=200 cells/microL or >/=14%, and
60 The immediate risk of an ADI for a given CD4 lymphocyte count has declined over time and is lower
61 of plasma HIV RNA level, in addition to the CD4+ lymphocyte count, has a role in guiding the managem
62 Specific studies at baseline should include CD4 lymphocyte count, HIV-1 RNA level, and gynecologic e
64 nsent was obtained for studies that entailed CD4 lymphocyte counts, immunophenotyping, isolator blood
67 ficiency virus type 1 (HIV-1) RNA levels and CD4+ lymphocyte counts in HIV-infected patients improved
68 NHL incidence rose steadily with decreasing CD4 lymphocyte counts; in contrast, BL incidence was low
69 tained virus suppression, and children whose CD4 lymphocyte counts increased >70 cells/microL by 20 w
71 points: plasma HIV-1 RNA level (viral load), CD4+ lymphocyte count, initiation of antiretroviral ther
74 sults were similar in patients with baseline CD4(+) lymphocyte counts less than 0.010 x 10(9) cells/L
76 bed PCP prophylaxis was higher in those with CD4 lymphocyte counts < 250 cells/microL or CD4 cell per
79 progression, comparable with that of cutoff CD4(+) lymphocyte count <350 lymphocytes/mm(3) and HIV-1
81 increased among HIV-seropositive women with CD4(+) lymphocyte counts <500 cells/mm(3) and among wome
82 Weibull proportional hazards model, baseline CD4+ lymphocyte count <200, black race, other nonwhite r
83 isolated from 10 HIV-infected patients with CD4+ lymphocyte counts < 200/mm3 without signs of active
84 rval, 1.14 to 3.16; P = 0.01), low antenatal CD4+ lymphocyte count (<29 percent of total lymphocytes)
85 vealed an inverse association between IE and CD4 lymphocyte count (odds ratio [OR] for 200-499 cells/
87 II and HIV RNA was measured in serum and the CD4 lymphocyte count of 25 HIV-infected patients was det
88 Five HIV-infected patients with baseline CD4 lymphocyte counts of less than 50 cells/mL were admi
89 iagnosed, all five patients had had absolute CD4 lymphocyte counts of less than 85 cells/microL, and
92 o were not using antiviral drugs and who had CD4+ lymphocyte counts of > or = 500 per microliter of b
96 ollers (VCs) (<5,000 HIV-1 RNA copies/ml and CD4+ lymphocyte counts of >400 cells/mul) capable of sol
97 f CMV infected persons with AIDS with either CD4+ lymphocyte counts of < or = 50 per cubic millimeter
98 women was 52.2% when their male partners had CD4+ lymphocyte counts of <200 cells/microL, 45.9% in wo
99 e virologic suppression, those with baseline CD4+ lymphocyte counts of <200 cells/mm3 tended to progr
100 to progress faster than those with baseline CD4+ lymphocyte counts of 201-350 cells/mm3 (P=.09) and
101 ease progression between those with baseline CD4+ lymphocyte counts of 201-350 cells/mm3 and those wi
103 t indicated the need to change the threshold CD4 lymphocyte counts or HIV-RNA levels for initiation o
105 in incidence of HIV-1 infection, virus load, CD4 lymphocyte count, or V3 loop amino acid sequence.
106 duction in HIV-1 RNA level or an increase in CD4+ lymphocyte count, or both, was associated with a de
107 nt relation between plasma HIV RNA level and CD4+ lymphocyte count over time and clinical outcome sug
111 Shortened survival was associated with low CD4 lymphocyte count (P<.0001), no ART (P<.0001), and cr
113 n to AIDS correlated strongly with base-line CD4+ lymphocyte counts (P = 0.001) and plasma levels of
115 ncorporating both HIV-1 RNA measurements and CD4+ lymphocyte counts provided better discrimination of
118 nonpregnant women according to age, baseline CD4(+) lymphocyte count, receipt of HAART, and date of c
119 optosis are associated with the magnitude of CD4 lymphocyte count recovery during antiretroviral ther
121 cardiovascular risk factors, HIV viral load, CD4 lymphocyte count, statin use, antihypertensive use,
122 in the incidence of ADIs overall and within CD4 lymphocyte count strata, the relationship with treat
124 hanges in the plasma HIV-1 RNA level and the CD4+ lymphocyte count, taken together, are valid predict
125 ents who died had significantly lower median CD4 lymphocyte counts than did HIV-seropositive patients
128 national Prognostic Index scores; the median CD4 lymphocyte count was 112/mm(3) (range, 19/mm(3) to 7
135 f developing CMV disease (P < 0.001) whereas CD4+ lymphocyte count was not a useful predictor (P = 0.
136 immunodeficiency virus (HIV) infection whose CD4 lymphocyte counts were between 200 and 500 cells/mm3
138 >10(6) copies/mL), and both baseline RNA and CD4+ lymphocyte count were independently predictive of s
139 om 1988 through 1998, the viral load and the CD4+ lymphocyte count were measured approximately every
143 ve men whose age, body-mass index (BMI), and CD4-lymphocyte count were within the range of values in
144 are based on the viral load, rather than the CD4+ lymphocyte count, will lead to differences in eligi
145 rends toward progressive modest increases in CD4+ lymphocyte counts with GM-CSF treatment at 16 weeks
146 ADIs was seen after stratification by latest CD4 lymphocyte count within each year (< or = 50, 51-200