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1 sion levels in H-HCA, IHCA, b-HCA, UHCA, and focal nodular hyperplasia.
2 recursor, hepatic adenoma, but not in benign focal nodular hyperplasia.
3 atients (42.2%) had adenomas, 29 (19.7%) had focal nodular hyperplasia, 25 (17.0%) had hemangiomas, 1
6 necrosis, in alcoholic liver disease, and in focal nodular hyperplasia are compared with liver progen
7 s encompassed cysts (70), hemangiomata (37), focal nodular hyperplasia (FNH) (23), adenomata (47), an
11 ed with nodular regenerative hyperplasia and focal nodular hyperplasia (FNH), which finally evolved t
12 radiologically indeterminate for adenoma or focal nodular hyperplasia (FNH): (1) continue to observe
15 nal uptake of SH U 508A is characteristic of focal nodular hyperplasia, is seen in some hemangiomas,
16 cclusive thrombosis, and lack of visibility; focal nodular hyperplasia-like nodules (six [14%] of 42
17 inoma (n = 6), cavernous hemangioma (n = 4), focal nodular hyperplasia (n = 2), hamartoma (n = 1), an
18 liver disease (n = 9), hydatid cyst (n = 6), focal nodular hyperplasia (n = 3), and adenoma (n = 9).
19 ellular carcinoma, n = 4; hemangioma, n = 9; focal nodular hyperplasia, n = 7) received 2.5 g SH U 50
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