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1 esented that this tumor represents a primary cardiac tumor.
2 helpful in detecting metastases of malignant cardiac tumors.
3 heart transplantation for inoperable primary cardiac tumors.
4 ial infarction, viral infection, and primary cardiac tumors.
5 ents underwent surgical resection of primary cardiac tumors; 163 (50%) with myxomas, 83 (26%) with pa
6 r both in malignant primary and in secondary cardiac tumors (8.0 +/- 2.1 and 10.8 +/- 4.9, P < 0.01).
10 h lipomas, 28 (9%) with other benign primary cardiac tumors, and 19 (6%) with primary malignant tumor
11 y myocarditis, anthracycline cardiomyopathy, cardiac tumors, and arrhythmogenic right ventricular dys
12 is </=18 years; 2) cardiac MRI evaluation of cardiac tumor; and 3) histologic diagnosis or diagnosis
19 ents aged </=18 years undergoing surgery for cardiac tumor between 1990 and 2005 from 16 centers were
23 little experience with diagnostic imaging of cardiac tumors in children, because of their low prevale
24 gnetic resonance imaging (MRI) evaluation of cardiac tumors in children, each with histology correlat
26 to describe a large experience with primary cardiac tumors in pediatric patients, characterize assoc
27 recurrence after partial resection of benign cardiac tumors indicates that a less risky tumor debulki
30 molecular genetic investigations of primary cardiac tumors (myxomas, lipomas, rhabdomyomas, and fibr
31 benign cardiac tumors (n = 7) and malignant cardiac tumors (n = 17) (cardiac primaries [n = 8] and m
32 Patients were divided into 2 groups: benign cardiac tumors (n = 7) and malignant cardiac tumors (n =
34 ody weight, but reversed insulin resistance, cardiac tumor necrosis factor-alpha expression, nuclear
40 24 consecutive patients with newly diagnosed cardiac tumors were analyzed (11 men, 13 women; mean age
41 y 50% of VHL(-/-) hearts developed malignant cardiac tumors with features of rhabdomyosarcoma and the
42 in BA+ tumors (P <or= 0.050) than in GEJ and cardiac tumors without associated Barrett's esophagus.
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