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1 mpled using three methods: swab, scrape, and punch biopsy.
2 otein from a single 3 mm full thickness skin punch biopsy.
3 cutaneous innervation in skin obtained using punch biopsy.
4 iated and nonirradiated areas by keratome or punch biopsy.
5 tion of individual hydrogels using the small punch biopsies.
6 ing accidental radiation exposure using skin punch biopsies.
7 mphomas that were collected with 4-6 mm skin punch biopsies.
11 d five of six doxycycline-treated dogs, skin punch biopsies and multiple tissues from necropsy sample
17 d at 4 days and 7 days after skin removal by punch biopsy disclosed EPCs incorporated into foci of ne
19 kin fibroblast samples were obtained by 2-mm punch biopsy from 12 patients (11 were women) who had ma
21 mentary DNAs from 92 psoriatic and 82 normal punch biopsies, generating an average of approximately 3
22 48) and equivalent to the reproducibility of punch biopsy histopathologic interpretations (kappa = 0.
23 bleeding and coagulation parameters, using a punch biopsy-induced bleeding model in healthy subjects.
33 le dogs was studied quantitatively with skin punch biopsy samples and blood samples collected at 4- a
34 future studies, small tissue samples, e.g., punch biopsy samples, might be sufficient for case confi
37 unch biopsy specimen was preferred to a 6-mm punch biopsy specimen since the wound was less likely to
39 relia burgdorferi was isolated from the skin punch biopsy specimens during each episode of erythema m
42 papillary dermal vascular structures in all punch biopsy specimens of allo-HSCT recipients who had c
43 dent infection was assayed by culture of ear punch biopsy specimens taken at 4, 8, and 12 weeks posti
51 status, and performed dermal biopsies (3-mm punch biopsy) with dermal carotenoids assessed by HPLC.
54 t skin biopsy specimens, including a routine punch biopsy, yield sufficient material for diagnostic f
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