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1 l antimicrobials in patients with type 1 and type 2 DM.
2 tion are similar in patients with type 1 and type 2 DM.
3 or function in subjects with both type 1 and type 2 DM.
4              The prevalence of type 1 DM and type 2 DM was compared between patients with incident RA
5  years with hypertension (>130/80 mm Hg) and type 2 DM (glycosylated hemoglobin [HbA1c], 6.5%-8.5%) a
6 s (peanuts, soybeans, and other legumes) and type 2 DM incidence.
7                               In obesity and type 2 DM, there is an increased content of lipid within
8  and to the pathogenesis of both obesity and type 2 DM.
9 pect of IR of skeletal muscle in obesity and type 2 DM.
10 luded proximal myotonic myopathy (PROMM) and type 2 DM (DM2) but without the DM1 mutation, showed lin
11                No association between RA and type 2 DM was observed.
12                  We induced type 1 (T1D) and type 2 DM (T2D) in a portfolio of genetic mouse models c
13 rvival in patients with type 1 DM (T1DM) and type 2 DM (T2DM) following CABG.
14 and in combination, which was designated as "type 2 DM phenotype" (n=5).
15        There is a modest association between type 2 DM and CRC among men, but not women.
16      When we allowed for interaction between type 2 DM and other key risk factors, DM remained a sign
17 nhibitor, is regulated in skeletal muscle by type 2 DM and ischemia.
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.
20 hus have a 10% annualized risk of developing type 2 DM.
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
24                             Risk factors for type 2 DM, such as positive family history of type 2 DM
25                           Predisposition for type 2 DM can coexist with the type 1 DM phenotype and i
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.
28 pendently associated with increased risk for type 2 DM.
29          Of these patients, 1731 (27.9%) had type 2 DM.
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
32 sedentary lifestyle and a marked increase in type 2 DM among children.
33 review recent findings that indicate that in type 2 DM and obesity, skeletal muscle manifests inflexi
34  moderate streptozotocin injection to induce type 2 DM.
35                        However, data linking type 2 DM risk and legume intake are limited.
36  the prevention of type 2 diabetes mellitus (type 2 DM).
37 (CP) patients with type-2 diabetes mellitus (type-2 DM) than controls (systemically healthy individua
38                                   Among men, type 2 DM was associated with increased risk of incident
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%)
41              We investigated associations of type 2 DM and insulin use with CRC risk.
42 -years of follow-up, there were 507 cases of type 2 DM.
43                 Improved glycemic control of type 2 DM is associated with substantial short-term symp
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/
46           Neither positive family history of type 2 DM nor overweight at baseline could predict islet
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
49                                 Incidence of type 2 DM did not differ between groups: 396 men in the
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
52 otein indeed involved in the pathogenesis of type 2 DM by inducing insulin resistance.
53   The multivariate-adjusted relative risk of type 2 DM for the upper quintile compared with the lower
54 rm exposure to air pollution and the risk of type 2 DM.
55                                    The RR of type 2 DM associated with long or highly irregular menst
56 ge 18 to 22 years, the relative risk (RR) of type 2 DM among women with a menstrual cycle length that
57                         The mean duration of type-2 DM among individuals in group-1 was 8.2 years (7
58 volving insulin use in adults with type 1 or type 2 DM from January 1, 1980, to January 8, 2003.
59 in 120 outpatients (240 eyes) with type 1 or type 2 DM.
60 eyes from 24 individuals with prediabetes or type 2 DM (glycated hemoglobin [HbA1c] >= 5.7) and 16 co
61                                     Overall, type 2 DM is still relatively infrequent; however, the h
62                                     Overall, type 2 DM was still relatively infrequent, but the highe
63 e and soy food consumption and self-reported type 2 DM.
64 ular, was inversely associated with the risk type 2 DM.
65 ears had no effect on the risk of subsequent type 2 DM.
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
73 periodontitis (118 normoglycemic and 89 with type 2 DM) were analyzed.
74 verall, 13% (sampled n = 171) of adults with type 2 DM (n = 1197) had CRI with a population estimate
75       The population estimate of adults with type 2 DM and CRI in the absence of diabetic retinopathy
76 e both absent in 30% (n = 51) of adults with type 2 DM and CRI.
77                      Among older adults with type 2 DM, femoral neck BMD T score and FRAX score were
78               34 008 men were diagnosed with type 2 DM in 39.4 million person-years of follow-up.
79 th GDM and GTD as well as in her father with type 2 DM but was absent in control patients.
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
83                      Sixty participants with type 2 DM and moderate to severe periodontal disease wer
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
86 d hemoglobin (HbA1c) levels of patients with type 2 DM (DMt2).
87 araoxon in serum samples of 87 patients with type 2 DM and 46 patients with pre-DM showing impaired f
88                             In patients with type 2 DM and CP, local delivery of 1% ALN into periodon
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
92                                Patients with type 2 DM have a less dysbiotic subgingival microbial pr
93                PON-1 status in patients with type 2 DM may contribute to this association.
94  The shallow and deep sites of patients with type 2 DM presented higher proportions of Actinomyces sp
95                                Patients with type 2 DM undergoing bioprosthetic valve implantation ar
96 ithm successfully matched 1113 patients with type 2 DM with the same number of no-DM patients.
97  consent from the patients, 37 patients with type 2 DM without overt heart disease and 23 age-matched
98                             In patients with type 2 DM, adding bedtime neutral protamine Hagedorn (is
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
101 roteinase (MMP)-2 and MMP-9 on patients with type 2 DM.
102 egimen that is well suited for patients with type 2 DM.
103 logic regimens for the at-risk patients with type 2 DM.
104 substantial burden of CRI among persons with type 2 DM in the United States is likely due to renal pa
105 ived from soy beans and their products) with type 2 DM was not significant.
106                       Group-1: Patients with type-2 DM and CP; group-2: Non-diabetic individuals with
107 evels of AGEs are higher in CP patients with type-2 DM compared to systemically healthy individuals w
108 rsus 2.9% (n=33) in patients with or without type 2 DM (P<0.001), respectively.
109 m with bleeding) of patients with or without type 2 DM were evaluated for levels/proportions of 40 ba
110 s in the GCF of CP patients with and without type-2 DM.
111                                 Among women, type 2 DM and insulin use were not associated with risk

 
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