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1 Eligible participants had information about self-reported dep
2 Eligible participants were women aged 18 years or older with
3 Eligible patients (aged >=18 years) had deleterious germline
4 Eligible patients had previously untreated acute myeloid leuk
5 Eligible patients were aged >=50 years.
6 Eligible patients were those with operable, node-positive-or
9 17, and Dec 31, 2017, 55 enumeration area clusters had 1118 eligible index cases that led to 342 interventions covering 8
15 records of the remaining 109 clinics, we identified 13 657 eligible patients who were sent an introductory letter with 1
19 We analyzed antiretroviral therapy (ART)-eligible adults newly linking to care at 64 clinics in Zambia
21 h epithelioid sarcoma were enrolled in the study and deemed eligible for inclusion in this cohort.
23 A detailed systematic search was performed to identify eligible randomized clinical trials (RCTs) reporting on the c
24 e 5,467 patients that were screened, 2,007 were molecularly eligible for entry into the trial, and 302 entered the trial
25 ieved SVR(12) , 10 had undetectable viral loads but are not eligible for SVR(12) , and 7 remain on treatment.
27 Review, quality assessment, and risk assessment for bias of eligible publications were performed along recommended guidel
28 lteplase was an additional 1.7 (P<0.01), and the percent of eligible patients treated with alteplase increased by 8% (P=0
30 50% federal poverty level (FPL)] and middle-income patients eligible only for premium subsidies (251%-400% FPL) were comp
33 he addition of daratumumab (D) to RVd (D-RVd) in transplant-eligible NDMM patients was evaluated.
34 n models of acute ovarian failure risk were developed using eligible female US and Canadian participants in the Childhood
37 4 livebirths and 43 spontaneous or elective abortions) were eligible for post-pregnancy viral load trajectory analyses (i
39 12 years with grades II to IV steroid-refractory aGVHD were eligible to receive ruxolitinib orally, starting at 5 mg twic
44 In the clinical study, 24 in vivo-in vitro pairs were eligible for further analysis, with 4 having been rejected as
50 ion to evaluate how WIC authorization affected sales of WIC-eligible foods in 8 DVS pilot stores, compared with 8 matched