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Clinically, SMARCA2 inactivation may predict poor prognosis, as loss of expression in both NSCLC and HCC correlates with worse OS (Endo et al., 2013; Fukuoka et al., 2004; Reisman et al., 2003).
It is unknown whether patient-mediated factors may predict poor adherence, and thus poor virological suppression, in the long-term.
The high expression level of S100A7 in poorly differentiated and lymph node positive breast tumors suggests that it may predict poor clinical outcome and a high risk of recurrence or progression in DCIS [7].
Although our conclusions differ from those from other groups, we speculate that the presence of high serum titer of Ma2 autoantibodies may predict poor prognosis in patients suffering from SI-NETs, as previously shown in different diseases.
Additionally, elevated circulating SPD levels may predict poor clinical outcomes.
Arterial occlusion at any (initial or follow-up) angiography may predict poor outcome and stroke recurrence.
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The result showed that high level of miR-200c may predict poorer OS, with the pooled HR being 1.14 (95% CI: 0.77 1.69).
Furthermore, RVD may also predict poor pulmonary clot resolution at 6 months, and a higher incidence or venous thromboembolism (VTE) recurrence was demonstrated when RVD was present [40].
Poor compliance with the management of HPN may well predict poor compliance with complex post-transplantation care regimens.
This evidence suggests that, in vivo, a loss of E-cadherin may predict a poor patient outcome on tamoxifen therapy, and may account for some of the additional benefits seen with aromatase inhibitors.
However, a second isolate, obtained after 5 days of treatment was resistant to cephalosporins, tetracycline, chloramphenicol and linezolid and the MIC for vancomycin had increased to 1.5 mcg/ml, a concentration that may predict a poor in vivo response.
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