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1 ving to be a highly significant biomarker in surgical pathology.
2 associated with the presence of unfavorable surgical pathology.
3 e of ages, associated disease processes, and surgical pathology.
4 ent EUS findings did not correlate well with surgical pathology.
5 esponse and EUS staging were correlated with surgical pathology.
6 36 (97.3%) had correct localization based on surgical pathology.
7 f pretreatment functioning (46.4% to 78.4%), surgical pathology (37.1% to 86.3%), radiation technique
10 any thickness) may improve the management of surgical pathology and guide microsurgery of any human t
11 of molecular genetics from the laboratory to surgical pathology and other clinical departments is a m
12 , results of cytologic examination of urine, surgical pathology, and total dose and duration of cyclo
13 hese data clearly demonstrate the primacy of surgical pathology as the major determinant of outcome i
14 reoperative imaging were identified from the surgical pathology database (mean age, 51 years; median,
15 Twenty-four patients with records in the surgical pathology database who had a diagnosis of mamma
16 ologically confirmed DN was identified using surgical pathology databases at the study sites; 590 cas
18 iasis, AD, and erythroderma belonging to the surgical pathology files of the James Homer Wright Patho
21 herapy for a variety of commonly encountered surgical pathologies including cardiovascular disease, n
25 ffin 1 antibody, a commonly used antibody in surgical pathology practice; and CPS1 expression appears
26 nic medical records and chart abstraction of surgical, pathology, radiology, and outpatient records,
28 formalin-fixed, paraffin-embedded and frozen surgical pathology replicates showed the complete preser
29 in within the specimen was identified by the surgical pathology reports and confirmed by re-examinati
37 The overall percent agreement of NCB and surgical pathology to determine tumor grade was poor (ka
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