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1 d processed for routine histology as well as direct immunofluorescence.
2 ributed on the surface of trypomastigotes by direct immunofluorescence.
3  Vascular chlamydial antigen was assessed by direct immunofluorescence.
4  for the presence of Chlamydia species using direct immunofluorescence.
5  should be monitored in patients with IgA on direct immunofluorescence.
6     Clinical evaluation, histopathologic and direct immunofluorescence analyses of skin specimens, an
7                                              Direct immunofluorescence analyses showed immunoglobulin
8 u A+B enzyme immunoassays were compared with direct immunofluorescence and cell culture for detection
9 was performed using conventional techniques (direct immunofluorescence and cell culture).
10 olves clinical presentation, histopathology, direct immunofluorescence and serological tests.
11                              H & E staining, direct immunofluorescence, and assessment of functional
12                                              Direct immunofluorescence antibody staining (DFA) and pr
13  within 24 h of receipt by cytospin-enhanced direct immunofluorescence antibody testing (DFA) and rea
14         Viral detection was done by culture, direct immunofluorescence assay (DFA) or polymerase chai
15                                  A new rapid direct immunofluorescence assay (DFA) respiratory screen
16 confirmed by matching results from classical direct immunofluorescence assay and nucleotide sequencin
17              MSVs, conventional culture, and direct immunofluorescence assay identified 96, 85, and 6
18 sed by enzyme-linked immunosorbent assay and direct immunofluorescence assay.
19 linical implications of positive or negative direct immunofluorescence biopsies (DIF) in patients wit
20 eagent was evaluated using cytospin-enhanced direct immunofluorescence (DFA), and the results were co
21 eal swabs were retested by cytospin-enhanced direct immunofluorescence (DFA; SimulFluor respiratory s
22 ival biopsy samples were obtained to perform direct immunofluorescence (DIF) and histologic analyses.
23                        Dermatologists submit direct immunofluorescence (DIF) biopsies on a daily basi
24   The u-serrated immunodeposition pattern in direct immunofluorescence (DIF) microscopy is a recogniz
25              A retrospective chart review of direct immunofluorescence (DIF) studies in buccal mucosa
26                                              Direct immunofluorescence (DIF) testing has been an impo
27                                              Direct immunofluorescence (DIF) testing is a useful adju
28 c desquamative gingivitis (CDG) are shown by direct immunofluorescence (DIF) to be immune mediated di
29 nically indistinguishable patients, who have direct immunofluorescence (DIF)-negative biopsies, be ex
30 als, routine hematoxylin and eosin (H&E) and direct immunofluorescence examinations were performed.
31                                              Direct immunofluorescence (IF) studies are valuable gold
32                                              Direct immunofluorescence immunoreactants and low titer
33 re, it is important to include serologic and direct immunofluorescence in the diagnostic algorithm of
34  any point after ICI treatment, confirmed by direct immunofluorescence, indirect immunofluorescence,
35 ta on at least a mucosal biopsy specimen for direct immunofluorescence microscopy (DIF) and indirect
36  the keratinocyte cell membrane, detected by direct immunofluorescence microscopy of a perilesional b
37 linical criteria are usually not sufficient, direct immunofluorescence microscopy of a perilesional b
38                                              Direct immunofluorescence microscopy serration pattern a
39                                              Direct immunofluorescence microscopy showed a linear n-s
40 evere arteropathic change, positive arterial direct immunofluorescence, obvious foci of severe capill
41        Data at presentation on demographics, direct immunofluorescence, ocular findings, sites of ext
42 uantitative PCR of spirochete DNA in joints, direct immunofluorescence of spirochetes in joints, and
43 biopsies were more likely to have a negative direct immunofluorescence result than patients with biop
44                                              Direct immunofluorescence revealed a speckled pattern of
45                                              Direct immunofluorescence showed positive staining for f
46 ay (DRSV) (Becton Dickinson and Company) and direct immunofluorescence staining (DFA) were compared w
47 y tested by viral culture (405 specimens) or direct immunofluorescence staining (DIF) (65 specimens).
48 llinois, we tested respiratory secretions by direct immunofluorescence staining from December to Marc
49                      A microwave-accelerated direct immunofluorescence staining method which requires
50                                              Direct immunofluorescence studies of lung tissue were ne
51                                              Direct immunofluorescence studies of peri-lesional tissu
52 gic information that cannot be obtained from direct immunofluorescence studies of skin biopsies, and
53 agnostic aids included routine histology and direct immunofluorescence studies to rule out immunobull
54                                              Direct immunofluorescence study results were negative fo
55               This disease is diagnosed with direct immunofluorescence testing showing a linear depos
56  of subepithelial separation with or without direct immunofluorescence testing were randomly chosen t
57                           Routine histology, direct immunofluorescence testing, and indirect immunofl
58 erpes simplex virus (HSV), cytospin-enhanced direct immunofluorescence using Chemicon HSV monoclonal
59 B viruses and respiratory syncytial virus by direct immunofluorescence using fluorescein isothiocyana
60                     Enhanced sensitivity for direct immunofluorescence was reported if skin biopsy sp
61                               The results of direct immunofluorescence were negative, excluding an Ig
62 e hematoxylin and eosin (H & E) staining and direct immunofluorescence were performed.
63          Oocyst excretion was quantitated by direct immunofluorescence with a C. parvum-specific mono
64 ing, PCR-based detection of donor genes, and direct immunofluorescence with quantum dots were used to
65                              Until recently, direct immunofluorescence with standard optical microsco