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1 were identified with a primary diagnosis of pancreatic neoplasm.
2 ma of the pancreas is the most common benign pancreatic neoplasm.
3 eatic ductal adenocarcinoma (PDAC), a deadly pancreatic neoplasm.
4 erstand the relevance of these signatures in pancreatic neoplasms.
5 s per year, and they account for 1-2% of all pancreatic neoplasms.
6 Two patients with choledochoceles (7%) had pancreatic neoplasms.
7 copic techniques for diagnosing and treating pancreatic neoplasms.
8 cience and clinical advances in the field of pancreatic neoplasms.
9 ly in the ladder of oncogenesis, as in human pancreatic neoplasms.
10 local ablative treatment of solid and cystic pancreatic neoplasms.
11 to achieve better outcomes for patients with pancreatic neoplasms.
13 benign pancreatic neoplasm (34%), malignant pancreatic neoplasm (31%), other neoplasm (15%), chronic
14 imary DP, the indications for DP were benign pancreatic neoplasm (34%), malignant pancreatic neoplasm
15 organ will certainly shape the management of pancreatic neoplasm and holds the promise of improved ou
16 s on this organ is changing the treatment of pancreatic neoplasms and holds the promise of improved o
17 efine the risk of premalignant and malignant pancreatic neoplasms and potential benefits and limitati
18 EST PRACTICE ADVICE 8: The target detectable pancreatic neoplasms are resectable stage I pancreatic d
20 Expression of large T antigen is highest in pancreatic neoplasms, but is also detectable in the norm
21 Screening can detect curable, noninvasive pancreatic neoplasms, but the optimal imaging approach i
22 Only few case reports of mucinous cystic pancreatic neoplasm containing an undifferentiated carci
25 standard resection for benign and low-grade pancreatic neoplasms, has been described in mainly small
28 APC/beta-catenin pathway in other nonductal pancreatic neoplasms including pancreatoblastomas and ac
29 influence the development and progression of pancreatic neoplasms initiated by an oncogenic allele of
30 gration of molecular radionuclide imaging of pancreatic neoplasms into mainstream clinical practice.
32 id-pseudopapillary tumors (SPTs) are unusual pancreatic neoplasms of low malignant potential that mos
33 events or severe hypoglycemia, pancreatitis, pancreatic neoplasms, or allergic reactions than was pla
37 These compound mutant mice developed a novel pancreatic neoplasm, serous cystadenoma (SCA), presentin
39 red in locally advanced or centrally located pancreatic neoplasms to achieve complete tumor clearance
42 ductal adenocarcinomas, and 6 miscellaneous pancreatic neoplasms) were microdissected from 29 formal
43 Primary tumors, usually lung, colorectal, or pancreatic neoplasms, were identified in 135 patients (2