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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 , only 5 of those cases were confirmed using punch biopsy.
4 cutaneous innervation in skin obtained using punch biopsy.
5 iated and nonirradiated areas by keratome or punch biopsy.
6 tion of individual hydrogels using the small punch biopsies.
7 ing accidental radiation exposure using skin punch biopsies.
8 mphomas that were collected with 4-6 mm skin punch biopsies.
9 ldSHOT, was optimized for 0.75 mm human skin punch biopsies.
10 mputed tomography of postmortem human tissue punch biopsies.
15 d five of six doxycycline-treated dogs, skin punch biopsies and multiple tissues from necropsy sample
16 arteriosclerosis not normally represented in punch biopsies and potentially driven by persistent graf
24 logy assessment, and small fiber tests: skin punch biopsy, corneal confocal microscopy, microneurogra
25 d at 4 days and 7 days after skin removal by punch biopsy disclosed EPCs incorporated into foci of ne
29 kin fibroblast samples were obtained by 2-mm punch biopsy from 12 patients (11 were women) who had ma
31 mentary DNAs from 92 psoriatic and 82 normal punch biopsies, generating an average of approximately 3
32 48) and equivalent to the reproducibility of punch biopsy histopathologic interpretations (kappa = 0.
33 bleeding and coagulation parameters, using a punch biopsy-induced bleeding model in healthy subjects.
40 ral blood mononuclear cells (PBMCs) and skin punch biopsies of IBH lesions and healthy skin from IBH-
46 le dogs was studied quantitatively with skin punch biopsy samples and blood samples collected at 4- a
47 future studies, small tissue samples, e.g., punch biopsy samples, might be sufficient for case confi
50 unch biopsy specimen was preferred to a 6-mm punch biopsy specimen since the wound was less likely to
52 relia burgdorferi was isolated from the skin punch biopsy specimens during each episode of erythema m
56 papillary dermal vascular structures in all punch biopsy specimens of allo-HSCT recipients who had c
57 dent infection was assayed by culture of ear punch biopsy specimens taken at 4, 8, and 12 weeks posti
62 participated in a mechanistic substudy where punch biopsies were collected (lesional and nonlesional
63 Fibroblasts cells isolated from 3-mm skin punch biopsies were cultured on a 3-D Matrigel matrix wi
66 o severe pruritus, lesional and non-lesional punch biopsies were taken from AA patients along with ag
70 status, and performed dermal biopsies (3-mm punch biopsy) with dermal carotenoids assessed by HPLC.
73 t skin biopsy specimens, including a routine punch biopsy, yield sufficient material for diagnostic f