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1 a were further stratified by risk factor and HIV status.
2 globulin G (IgG) to VSA were not affected by HIV status.
3 h XDR tuberculosis are poor, irrespective of HIV status.
4 between elevated BP and AMI risk differs by HIV status.
5 ults, and has high mortality irrespective of HIV status.
6 treatment, age (0-4 years, 5-14 years), and HIV status.
7 orne infections, independent of their HCV or HIV status.
8 gle clinicopathological entity regardless of HIV status.
9 d disease outcome were compared according to HIV status.
10 t of syphilis according to disease stage and HIV status.
11 mined the association of these variants with HIV status.
12 fy high-risk youths who are unaware of their HIV status.
13 S on multivariate analysis including IPS and HIV status.
14 younger age at treatment start, and negative HIV status.
15 100-child-years in relation to time-updated HIV status.
16 pulation expectations, but did not differ by HIV status.
17 was not significantly affected by enrollment HIV status.
18 ld not be withheld or deintensified based on HIV status.
19 Participants self-reported HIV status.
20 Patients age 55 to 75 years with unknown HIV status.
21 nge in HIV Infection), stratified by sex and HIV status.
22 % CI, 41% to 69%; P < .001), irrespective of HIV status.
23 s, adjusted for study site, risk cohort, and HIV status.
24 itamin A, selenium, and zinc irrespective of HIV status.
25 d tested for antiretroviral drugs to confirm HIV status.
26 a-tocopherol did not differ significantly by HIV status.
27 ents with tuberculosis and was unaffected by HIV status.
28 d tumor cell PD-L1 expression, regardless of HIV status.
29 aces than do healthy subjects, regardless of HIV status.
30 performance of the assay was not affected by HIV status.
31 assessing organ donor risk, irrespective of HIV status.
32 nce interval, 1.1-10), after controlling for HIV status.
33 t the site of MTB infection, irrespective of HIV status.
34 G or IgA to rotavirus, which did not vary by HIV status.
35 more common in LAIV recipients regardless of HIV status.
36 diologic evidence of infection regardless of HIV status.
37 persons and from 35 persons of indeterminate HIV status.
38 cts (P < 0.01), but were not associated with HIV status.
39 icantly according to treatment assignment or HIV status.
40 ystematically reviewed for information about HIV status.
41 n of T. pallidum did not differ according to HIV status.
42 ed, 7% were HIV-negative, and 7% had unknown HIV status.
43 lockade in anal SCC, irrespective of patient HIV status.
44 d according to an individual's self-reported HIV status.
45 d by additional information on self-reported HIV status.
46 nce of obstructive disease did not differ by HIV status.
47 xposure questionnaires, and an assessment of HIV status.
48 mbination antiretroviral therapy (cART), and HIV status.
49 in the absence of documentation of positive HIV status.
50 5.2) of these individuals already knew their HIV status.
51 ates to determine differences by frailty and HIV status.
52 the NP examiner was blinded to screening and HIV status.
53 ell tolerated and active in KS regardless of HIV status.
54 cted people in sub-Saharan Africa know their HIV status.
55 The analysis was stratified according to HIV status.
56 rsion and reversion were not associated with HIV status.
57 his relationship held when we controlled for HIV status.
58 s specific disease or diseases stratified by HIV status.
59 5% CI, -.30 to .10] years) did not differ by HIV status.
60 minates were rare (0.2%) and not affected by HIV status.
61 mulative incidence and hazard rates, each by HIV status.
62 cular inflammation (28 eyes), independent of HIV status.
63 tudy evaluating MI risk from 1996 to 2011 by HIV status.
64 men with known human immunodeficiency virus (HIV) status, 15% of those without measles and 19% of tho
65 HIV and (1) maternal orphanhood and maternal HIV status, (2) reported sexual behaviour, and (3) repor
67 dividuals gained knowledge of their positive HIV status, 2818 were linked to care, 2151 became eligib
69 morbidities (41.8%), ASA status (11.3%), and HIV status (7.8%), with a smaller proportion stratifying
70 individuals living with HIV will know their HIV status, 90% of people with diagnosed HIV infection w
71 3 +/- 1.7 nmol/L; n = 121) subjects, nor was HIV status a significant predictor of plasma 25(OH)D whe
72 ence in pneumococcal acquisition by maternal HIV status (adjusted rate ratio (aRR) = 1.00, 95% confid
74 e proportions of participants who knew their HIV status after the CHiP visit; proportions linking to
80 need for assumptions concerning knowledge of HIV status and ART coverage among adults not consenting
81 communities in BAL differed significantly by HIV status and by COPD, with Pneumocystis jirovecii sign
82 c regression to examine associations between HIV status and cancer treatment, adjusted for cancer sta
84 r anal cytological diagnoses at study entry, HIV status and CD4 count, and detection of HPV types oth
86 In multivariable analysis, controlling for HIV status and continent of origin, people from Africa h
87 n to examine the association between patient HIV status and death resulting from the presenting cance
88 ght the importance of improving awareness of HIV status and expanding ART to prevent losses in HRQoL
89 infant pneumococcal acquisition by maternal HIV status and household exposure in Karonga District, M
92 Axis I disorders after controlling for both HIV status and lifetime Axis I history (adjusted odds ra
97 graphics, medical history and comorbidities, HIV status and related measures (CD4 cell counts, HIV vi
101 Children were recruited irrespective of HIV status and started on a standard antimicrobial regim
102 rate ratio (RR) for the association between HIV status and TB was estimated by time since HIV seroco
103 prevalence of homeostasis loss according to HIV status and the occurrence of AIDS in more than 5,000
105 resulted in significant interactions between HIV status and time of study in left insula, left pariet
107 the impact of human immunodeficiency virus (HIV) status and type on the clearance of HPV infection a
109 IV in adults, with neonates (irrespective of HIV status), and with Salmonella Typhimurium ST313.
110 ts were not uniformly performed according to HIV status, and adequate fasting before lipoprotein test
113 Vitamins with information on infant feeding, HIV status, and at least one visit in the first year wer
115 Adult index characteristics such as sex, HIV status, and extent or severity of disease were not a
116 ings support the need for HCWs to know their HIV status, and for HIV-infected HCWs to be offered anti
120 We intended to stratify the analyses by age, HIV status, and rural or urban setting; however, few stu
127 The OMT results were compared with true HIV status as determined by serum testing and/or clinica
128 r delivery were included if they had unknown HIV status at presentation (there was no age limit for t
130 at elevated partnership dissolution rates in HIV status aware serodiscordant couples reduce the sprea
132 o account, each percentage point increase in HIV status awareness reduces HIV incidence by 0.13 and 0
133 solution, every percentage point increase in HIV status awareness reduces HIV incidence in monogamous
134 completion of therapy, grade, race, age, and HIV status between the normal and abnormal Fhit expressi
136 nicillin for early syphilis, irrespective of HIV status, but data from coinfected patients are limite
139 Uganda, to evaluate the association between HIV status, CD4 cell count, and other clinical predictor
141 2007-2009, 1,777 pregnant women with unknown HIV status completed an interviewer-administered questio
143 for confounding variables including contact HIV status, contact age, socio-economic status, and inde
144 h undocumented human immunodeficiency virus (HIV) status could enable immediate provision of antiretr
149 l with near-perfect ART adherence and mutual HIV status disclosure among all participating couples.
151 le-blood glutathione, and whole-blood GPX to HIV status, disease severity, immune activation, and oxi
154 During the iPrEx study, there were 51,260 HIV status evaluations among 2,499 volunteers using RTs:
156 either HIV-positive MSM or MSM regardless of HIV status, for age bands 16-25, 16-30, 16-35, and 16-40
157 Duration of response is not influenced by HIV status; furthermore, HIV+ patients show no adverse e
158 clinical parameters, such as patient's age, HIV status, gender, disease duration, pretreatment plate
159 ntly modifies the disposition of SP, whereas HIV status has little influence on pharmacokinetic param
160 on were age </= 50 years, male sex, positive HIV status, history of hemophilia, sickle cell anemia or
161 severe disease (2.47, 1.17-5.24, p=0.0181), HIV status (HIV infected 10.3, 3.26-32.51; HIV exposed,
166 e as a confirmation test provided conclusive HIV status in only 50.0% (CI, 30.8% to 69.2%) of patient
167 BT could substantially increase awareness of HIV status in previously undiagnosed individuals in sub-
170 erved changes in IPD incidence, according to HIV status, in children aged 3 months-5 years and in wom
172 ates that after acute myocardial infarction, HIV status influences long-term risk, although the short
173 orate auxiliary information on self-reported HIV status into analyses based on partially observed HIV
175 criteria that preclude organ donation, only HIV+ status is singled out as a mandated exclusion to do
176 population stages (first positive HIV test, HIV status knowledge, and linkage to care) and three cli
177 rs for AR to INJ SLDs included age, positive HIV status, MDR tuberculosis and initial treatment with
178 infant CMV acquisition independent of infant HIV status (multivariable hazard ratio, 1.61; 95% confid
179 edictors: having a male partner with unknown HIV status, number of lifetime sexual partners, syphilis
180 tors including human immunodeficiency virus (HIV) status (odds ratio [OR], 7.90; P < .001), and basel
185 association between neonatal GBS disease and HIV-status of the mother and studies that assessed the a
186 in Nairobi, Kenya, to examine the impact of HIV status on (1) introducing influenza to the home and
194 nfluencing adherence were: non-disclosure of HIV status (OR = 17.99, p = 0.014); alcohol use (OR = 12
196 (p=0.001), proportion of women (p=0.01), and HIV status (p=0.03) were noted between the 14 prevalent
198 In multivariate analysis including maternal HIV status, placental malaria, and antibody responses, H
199 es in the levels of morbidity compression by HIV status, PLHIV-especially women living with HIV-spent
202 ected sex with a partner of negative/unknown HIV status) reported 12 months after inclusion between p
203 (regardless of human immunodeficiency virus [HIV] status) seen in a uveitis referral center between 1
204 infant pneumococcal acquisition by maternal HIV status, serotype-specific household exposure, and ot
205 prevalence varied significantly (P < .05) by HIV status, sexual orientation, and lifetime number of s
207 a clear difference in response depending on HIV status, suggesting that EE with superimposed HIV ent
209 in HIV-positive couples, and irrespective of HIV status, the majority of couples exhibit HPV concorda
212 In addition, VL+ YMSM who disclosed their HIV status to sex partners were more likely to report CA
215 lood pressure, human immunodeficiency virus (HIV) status, urine albumin-to-creatinine ratio, hemoglob
226 for incarceration, residence, and geography, HIV status was no longer significantly associated with c
229 HCV infection and alcohol abuse/dependence, HIV status was not independently associated with hepatoc
233 s with one or more survey participants whose HIV status was unknown were eligible to participate in t
234 patients and 1 isolate from a patient whose HIV status was unknown were shown to be consistent by ph
236 es in mean age at, and risk of, diagnosis by HIV status were estimated using multivariate linear regr
237 the levels of blood lipids and biomarkers by HIV status were examined before and after adjustment for
238 tic regression adjusting for child age, sex, HIV status, whether the child had been hospitalized in t
239 women present late for delivery with unknown HIV status, which limits the use of intrapartum nevirapi
240 All cases of tuberculosis, regardless of HIV status, which occurred between January 1992 and June
241 but 60 of 118 (50.8%) of the women of known HIV status who died during pregnancy or post partum were
242 eriolar and venular diameters in relation to HIV status, with a tendency towards narrower retinal dia
243 s, women often present in labor with unknown HIV status without receiving the HIVNET 012 nevirapine (
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