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6 enic factor CCBE1 or VEGFR3 function, appear cyanotic and die shortly after birth due to failure of l
9 justed rate ratio, 95% confidence interval): cyanotic CHD (6.44, 3.95-10.50), endocardial cushion def
11 is did not influence outcome in infants, but cyanotic children showed worse reperfusion injury and cl
15 Between 1988 and 1995, 162 patients with cyanotic congenital heart disease (mean age 37 years, ra
16 g nonlinear mixed effects model, presence of cyanotic congenital heart disease (odds ratio, 7.35; p <
17 igned infants 92 days of age or younger with cyanotic congenital heart disease and a systemic-to-pulm
18 erebrovascular events in adult patients with cyanotic congenital heart disease and to evaluate any co
22 he recommendation that routine screening for cyanotic congenital heart disease be added to the panel
23 and BNP are markedly elevated in adults with cyanotic congenital heart disease despite reduced body w
24 ascular events are a serious complication of cyanotic congenital heart disease in infants and childre
27 Chronic hypoxia (CH) present in infants with cyanotic congenital heart disease may be responsible for
30 ble increase in basal coronary blood flow in cyanotic congenital heart disease, flow reserve remains
34 who undergo heart surgery have a congenital cyanotic defect in which the heart is chronically perfus
35 ho undergo cardiac surgery have a congenital cyanotic defect where the heart is chronically perfused
41 Lack of past cardiac surgery (p = 0.04), cyanotic heart disease (p = 0.03), and early postoperati
42 ffered to patients with a variety of complex cyanotic heart disease at younger ages, and has resulted
43 ry syncytial virus infection, or presence of cyanotic heart disease or residual right-to-left intraca
45 diopathic pulmonary hypertension, congenital cyanotic heart disease, morbid obesity associated with s
49 phometric or hemodynamic differences between cyanotic infants with critical PS and asymptomatic infan
55 here was no difference in oxytocin levels in cyanotic patients compared with control subjects (P=0.49
60 tion and hematocrit significantly greater in cyanotic patients than in control subjects (82+/-6 versu
64 hest potential for vascular injury: younger, cyanotic patients with longer pump times and longer post
66 ein kinases (MAP kinases) in 15 infants with cyanotic (SaO2<85%) or acyanotic (SaO2>95%) heart defect
67 ent animals and found that these mice become cyanotic shortly before death because of lung maturation
68 Caesarean section at embryonic day 18.5 were cyanotic, suffered from respiratory distress, and failed
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