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1 duals diagnosed with the condition remain in poor control.
2 ardiovascular events than those with fair or poor control.
3 ategies at exacerbation or in the context of poor control.
4 ulting in slow polymerization and relatively poor control.
5 recognized as a risk for asthma severity and poor control.
6 , whereas those with the worst score (4) had poor control (29.4%) and high hazard of hemorrhage (haza
7 L) within the past year; only 9% experienced poor control (a HbA1c level > 12% or mean blood glucose
8 rom asthma, comorbidities that contribute to poor control and lifestyle/environmental factors that re
9 Inefficient induction of ISGs contributes to poor control and persistence of hepatitis C virus infect
11 ints that are magnified in wildlife, such as poor control and substantial trait variation within and
13 health risks and management challenges, with poor control attributed to survival of treatment-resista
18 ded to identify the barriers contributing to poor control even in populations with access to care.
19 GHb <7) soon after induction of diabetes, or poor control for 6 months with 6 months' good control.
20 ozotocin-induced diabetes were in a state of poor control (GHb >11%) for 12 months, good control (GHb
21 4 years of follow-up, subjects who were in "poor" control (glycosylated hemoglobin (GHb) > or = 11%)
23 roid therapy (ICS) is a major contributor to poor control in difficult asthma, yet it is challenging
24 ivity observed in particular cases is due to poor control in ylide conformation or due to partial rev
25 ndings suggest that in diabetic adolescents, poor control is associated with a significant depletion
28 d CXCL1/keratinocyte-derived chemokine (KC), poor control of bacterial replication, and exacerbated i
29 ertension, lack of appropriate diagnosis and poor control of blood pressure among those with a diagno
33 association between social risk factors and poor control of cardiovascular disease (CVD) risk factor
35 ily driven by fishing vessel flags linked to poor control of corruption by the flag state, high owner
37 factor for several autoimmune diseases, and poor control of EBV viral load and enhanced anti-EBV res
39 alian cells by high background fluorescence, poor control of expression, and low GFP maturation effic
44 tion, CD8(+) T-cell alveolitis, smoking, and poor control of human immunodeficiency virus (HIV) are f
45 ack race, were independently associated with poor control of hypertension among those who were aware
49 has recently been challenged with reports of poor control of reflux and the inability to prevent prog
50 functions, and lack of either element led to poor control of responder cell proliferation and cytokin
51 s suffer from a number of limitations (e.g., poor control of solid tumors), and while combining ACT w
57 s often a trial-and-error process limited by poor control of the local catalyst environment and few s
58 with diabetes are at risk for DKD because of poor control of their blood glucose, as well as nonmodif
59 , the expression of Tim-3 is associated with poor control of viral burden and impaired antiviral immu
62 ected individuals or humanized mice reported poor control of virus replication and the rapid emergenc
63 Negative immune regulation can result in the poor control of virus replication in chronic infections
64 database who began insulin (2000-2007) after poor control on oral glucose-lowering agents (OGLD) were
65 h often suffer from preservation issues, and poor control on the timing of oxidation leaves geochemic
66 We report that, relative to GTs, STs have poor control over attentional performance, due in part t
68 information density, few functional groups, poor control over folding, and difficulties in forming c
69 otein matrices that suffer from variability, poor control over matrix biochemistry, and inability to
71 e reintubated within the same day because of poor control over secretions, airway spasm, or hypoventi
72 ibitory control deficits possibly underlying poor control over stereotyped and repetitive and compuls
74 rs comprised participants who showed similar poor control over symptoms with the distribution of the
76 olloidal assemblies, but also because of the poor control over the assembly of nanocrystals within a
77 n material modulation(5), which suffers from poor control over the energy and position of trapping po
79 +/- 1.0 kg/ m(2), HbA(1c) 5.9 +/- 0.2%) and poor control (PC) (n = 10, age 50.0 +/- 2.5 years, BMI 2
80 ld male patient with diabetes mellitus under poor control presented to our emergency room with fever,
82 marked decrease in PEPCK content, suggesting poor control strength for this enzyme in gluconeogenic r
83 otein, supporting the concept that PEPCK has poor control strength over the gluconeogenic pathway in
88 In contrast, patient level predictors of poor control were: short acting bronchodilator overuse [