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5 years with hypertension (>130/80 mm Hg) and type 2 DM (glycosylated hemoglobin [HbA1c], 6.5%-8.5%) a
10 luded proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed lin
17 p and 402 men in the placebo group developed type 2 DM (relative risk, 0.98; 95% confidence interval,
18 significantly increased risk for developing type 2 DM that is not completely explained by obesity.
20 were included (199 for type 1 DM and 144 for type 2 DM, and 38 from other sources) if they involved h
21 insulin resistance is the major etiology for type 2 DM and numerous evidences showed that HCV infecti
22 esistance, characterized by risk factors for type 2 DM, can predict islet graft survival in type 1 DM
25 rength was associated with a 3-fold risk for type 2 DM (adjusted hazard ratio, 3.07 [CI, 2.88 to 3.27
26 associated with increased long-term risk for type 2 DM, even among those with normal body mass index.
29 risk of incident CRC compared to not having type 2 DM (RR: 1.24; 95% CI: 1.08-1.44); risk was higher
30 ith LV systolic and diastolic dysfunction in type 2 DM; this may explain in part the relationship of
32 review recent findings that indicate that in type 2 DM and obesity, skeletal muscle manifests inflexi
37 Thirty-three percent of type 1 and 48% of type 2 DM patients had significant stenosis (> or = 70%)
41 aboratory data, as well as family history of type 2 DM (first degree relatives), were collected from
42 ype 2 DM, such as positive family history of type 2 DM (n=11) and overweight (body mass index >25 kg/
44 We followed 64,227 women with no history of type 2 DM, cancer, or cardiovascular disease at study re
45 solute difference in cumulative incidence of type 2 DM between the lowest and highest tertiles of bot
47 ta-carotene supplementation and incidence of type 2 DM persisted despite multivariate adjustment.
48 the involvement of E2 in the pathogenesis of type 2 DM and underlying mechanisms were investigated in
50 The multivariate-adjusted relative risk of type 2 DM for the upper quintile compared with the lower
53 ge 18 to 22 years, the relative risk (RR) of type 2 DM among women with a menstrual cycle length that
61 Approaches to screening renal disease in the type 2 DM population should incorporate assessment of GF
62 r, when both risk factors were grouped, the "type 2 DM phenotype" was associated with earlier islet g
63 , respectively) were examined in relation to type 2 DM identified from outpatient and inpatient diagn
64 ntensity exercise is normal in uncomplicated type 2 DM but is impaired in those with microvascular co
65 227 with type 2 DM) and 1242 women (108 with type 2 DM) were diagnosed with colon or rectal cancer by
66 rs; mean body mass index, 32 [SD, 5.1]) with type 2 DM (mean duration, 7.7 [SD, 7.2] years; mean glyc
67 he final analytic cohort; 1567 men (227 with type 2 DM) and 1242 women (108 with type 2 DM) were diag
68 verall, 13% (sampled n = 171) of adults with type 2 DM (n = 1197) had CRI with a population estimate
73 opic changes to ensure that individuals with type 2 DM and CRI not due to diabetic glomerulosclerosis
74 filtration rate (GFR) among individuals with type 2 DM may not always be due to classic diabetic glom
75 l periodontal treatment of participants with type 2 DM and moderate to severe periodontal disease imp
77 6; 95% CI: 1.05-1.78), and participants with type 2 DM not using insulin (RR: 1.22, 95% CI: 1.04-1.45
78 1.44); risk was higher for participants with type 2 DM using insulin (RR: 1.36; 95% CI: 1.05-1.78), a
80 araoxon in serum samples of 87 patients with type 2 DM and 46 patients with pre-DM showing impaired f
82 at 2 years was assessed in 187 patients with type 2 DM and stable coronary artery disease on maintena
83 external validation cohort of patients with type 2 DM but not in an external validation cohort of pa
84 ntrolled, multicenter trial in patients with type 2 DM conducted at 28 clinical sites in the multirac
88 consent from the patients, 37 patients with type 2 DM without overt heart disease and 23 age-matched
90 n 18-month treatment period in patients with type 2 DM, pioglitazone slowed progression of CIMT compa
94 substantial burden of CRI among persons with type 2 DM in the United States is likely due to renal pa
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