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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
18 p and 402 men in the placebo group developed type 2 DM (relative risk, 0.98; 95% confidence interval,
19 significantly increased risk for developing type 2 DM that is not completely explained by obesity.
21 were included (199 for type 1 DM and 144 for type 2 DM, and 38 from other sources) if they involved h
22 insulin resistance is the major etiology for type 2 DM and numerous evidences showed that HCV infecti
23 esistance, characterized by risk factors for type 2 DM, can predict islet graft survival in type 1 DM
26 rength was associated with a 3-fold risk for type 2 DM (adjusted hazard ratio, 3.07 [CI, 2.88 to 3.27
27 associated with increased long-term risk for type 2 DM, even among those with normal body mass index.
30 risk of incident CRC compared to not having type 2 DM (RR: 1.24; 95% CI: 1.08-1.44); risk was higher
31 ith LV systolic and diastolic dysfunction in type 2 DM; this may explain in part the relationship of
33 review recent findings that indicate that in type 2 DM and obesity, skeletal muscle manifests inflexi
37 (CP) patients with type-2 diabetes mellitus (type-2 DM) than controls (systemically healthy individua
39 ed type 1 DM (DM1) and transgenic Lep(ob/ob) type 2 DM (DM2) diabetic murine models as donors and non
40 Thirty-three percent of type 1 and 48% of type 2 DM patients had significant stenosis (> or = 70%)
44 aboratory data, as well as family history of type 2 DM (first degree relatives), were collected from
45 ype 2 DM, such as positive family history of type 2 DM (n=11) and overweight (body mass index >25 kg/
47 We followed 64,227 women with no history of type 2 DM, cancer, or cardiovascular disease at study re
48 solute difference in cumulative incidence of type 2 DM between the lowest and highest tertiles of bot
50 ta-carotene supplementation and incidence of type 2 DM persisted despite multivariate adjustment.
51 the involvement of E2 in the pathogenesis of type 2 DM and underlying mechanisms were investigated in
53 The multivariate-adjusted relative risk of type 2 DM for the upper quintile compared with the lower
56 ge 18 to 22 years, the relative risk (RR) of type 2 DM among women with a menstrual cycle length that
60 eyes from 24 individuals with prediabetes or type 2 DM (glycated hemoglobin [HbA1c] >= 5.7) and 16 co
66 Approaches to screening renal disease in the type 2 DM population should incorporate assessment of GF
67 r, when both risk factors were grouped, the "type 2 DM phenotype" was associated with earlier islet g
68 , respectively) were examined in relation to type 2 DM identified from outpatient and inpatient diagn
69 ntensity exercise is normal in uncomplicated type 2 DM but is impaired in those with microvascular co
70 227 with type 2 DM) and 1242 women (108 with type 2 DM) were diagnosed with colon or rectal cancer by
71 rs; mean body mass index, 32 [SD, 5.1]) with type 2 DM (mean duration, 7.7 [SD, 7.2] years; mean glyc
72 he final analytic cohort; 1567 men (227 with type 2 DM) and 1242 women (108 with type 2 DM) were diag
74 verall, 13% (sampled n = 171) of adults with type 2 DM (n = 1197) had CRI with a population estimate
80 opic changes to ensure that individuals with type 2 DM and CRI not due to diabetic glomerulosclerosis
81 filtration rate (GFR) among individuals with type 2 DM may not always be due to classic diabetic glom
82 l periodontal treatment of participants with type 2 DM and moderate to severe periodontal disease imp
84 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
85 1.44); risk was higher for participants with type 2 DM using insulin (RR: 1.36; 95% CI: 1.05-1.78), a
87 araoxon in serum samples of 87 patients with type 2 DM and 46 patients with pre-DM showing impaired f
89 at 2 years was assessed in 187 patients with type 2 DM and stable coronary artery disease on maintena
90 external validation cohort of patients with type 2 DM but not in an external validation cohort of pa
91 ntrolled, multicenter trial in patients with type 2 DM conducted at 28 clinical sites in the multirac
94 The shallow and deep sites of patients with type 2 DM presented higher proportions of Actinomyces sp
97 consent from the patients, 37 patients with type 2 DM without overt heart disease and 23 age-matched
99 n 18-month treatment period in patients with type 2 DM, pioglitazone slowed progression of CIMT compa
100 ing and softening of the PF in patients with type 2 DM, supporting the hypo-thesis that diabetes-indu
104 substantial burden of CRI among persons with type 2 DM in the United States is likely due to renal pa
107 evels of AGEs are higher in CP patients with type-2 DM compared to systemically healthy individuals w
109 m with bleeding) of patients with or without type 2 DM were evaluated for levels/proportions of 40 ba