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1 h, and 94 (92%) had sputa smear-positive for acid fast bacilli.
2 on associated with areas of inflammation and acid-fast bacilli.
3 f 596 blocks containing nerve, 36% contained acid-fast bacilli.
4  than H37Ra, based on the numbers of CFU and acid-fast bacilli.
5 nd were examined for granuloma formation and acid-fast bacilli.
6 ost cases were not sputum-smear positive for acid-fast bacilli.
7 system using Middlebrook broth selective for acid-fast bacilli (13A medium).
8 mycobacterial growth and those with positive acid fast bacilli (AFB) growth were tested to detect myc
9                                              Acid Fast Bacilli (AFB) microscopy smear remains the mos
10 ns submitted for microscopy for detection of acid-fast bacilli (AFB) and for mycobacterial culture an
11                            Sputum smears for acid-fast bacilli (AFB) are the primary methods for diag
12           Contamination of broth cultures of acid-fast bacilli (AFB) by bacterial species other than
13                                 Detection of acid-fast bacilli (AFB) by sputum smear supports treatme
14 sputum corresponded well with the numbers of acid-fast bacilli (AFB) counted by microscopy.
15 rotizing and non-necrotizing granulomas, and acid-fast bacilli (AFB) culture from the surgically remo
16                     Smears were positive for acid-fast bacilli (AFB) in 63% (677 of 1,082) of specime
17                Manual reading of fluorescent acid-fast bacilli (AFB) microscopy slides is time-intens
18  Xpert, Lowenstein-Jensen (L-J) culture, and acid-fast bacilli (AFB) microscopy.
19 pic examination of respiratory specimens for acid-fast bacilli (AFB) plays a key role in the initial
20              A total of 575 participants had acid-fast bacilli (AFB) positive Mycobacterial Growth In
21 red to 2 sputum samples, each evaluated with acid-fast bacilli (AFB) smear and mycobacterial culture
22  of tuberculosis (TB) are more accurate than acid-fast bacilli (AFB) smear microscopy and are faster
23                                       Sputum acid-fast bacilli (AFB) smear microscopy has suboptimal
24 y isolation pending results of serial sputum acid-fast bacilli (AFB) smear microscopy is standard pra
25 ies for identification of MTBC directly from acid-fast bacilli (AFB) smear-positive broth cultures, i
26 Grocott's methenamine silver (GMS) stain and acid-fast bacilli (AFB) stain of the tissue itself were
27              Investigations such as culture, acid-fast bacilli (AFB) staining, and histopathology hav
28 farct, adrenal necrosis, and hemorrhage, and acid-fast bacilli (AFB) were seen in the lung, liver, ki
29 ing collections; and quantitative smears for acid-fast bacilli (AFB) with quantitative cultures.
30 ogy, immunohistochemistry (IHC) staining for acid-fast bacilli (AFB), and mycobacterial polymerase ch
31 ure for M. ulcerans, or a smear positive for acid-fast bacilli (AFB), together with a possible histol
32 esses digital microscopic images to identify acid-fast bacilli (AFB).
33 l of 106 specimens were culture positive for acid-fast bacilli (AFB).
34  generally requires specialized cultures for acid-fast bacilli (AFB; AFB cultures).
35 60 and Middlebrook 7H11 biplates), smear for acid-fast bacilli (AFB; auramine O), and clinical course
36 tions from silica-exposed mice had many more acid fast bacilli(+) (AFB(+)) organisms than from contro
37  hu10Tg mice showed marked increases in both acid-fast bacilli and host macrophages.
38 agement of highly infectious agents, such as acid-fast bacilli and systemic fungi, were revealed.
39  44 nerves from armadillos were screened for acid-fast bacilli and thin sections were examined ultras
40              Bronchoscopic washings revealed acid-fast bacilli and were culture positive for M tuberc
41 ee sputum specimens, which were examined for acid-fast bacilli by use of direct auramine and Ziehl-Ne
42 nfirmed cases, and yield of sputum smear for acid-fast bacilli cases.
43      Only 46 (32%) of these 143 patients had acid-fast bacilli detected in smears; acid-fast bacilli
44  patients with smears that were positive for acid-fast bacilli had a median treatment interval of 3 d
45 l-defective bacteria which later reverted to acid-fast bacilli have been isolated from sarcoid tissue
46 s included smears of aspirated materials for acid-fast bacilli in 11, mycobacterial culture in 14, an
47 sed on passive case finding and detection of acid-fast bacilli in sputum samples to diagnose pulmonar
48 sure the progressive reduction of numbers of acid-fast bacilli in the sputum smear and the clearance
49  had a respirator-fit testing program but no acid-fast bacilli isolation rooms.
50 ulated the percentage of lipid body-positive acid-fast bacilli (%LB + AFB) on sputum smears.
51                 Cultures of valve tissue for acid-fast bacilli might be considered in some cases of a
52 imen inclusion were (i) a positive smear for acid-fast bacilli (n = 54) and (ii) the source if the sm
53 rculosis but sputum smears were negative for acid-fast bacilli on 3 consecutive days) and 22,716 case
54                     Of 60 samples, 15 showed acid-fast bacilli on special staining.
55 losis, it often manifests without detectable acid-fast bacilli on sputum microscopy.
56 heterogeneous morphology and distribution of acid-fast bacilli; only at the surface of cavities, i.e.
57 ted using the MTBDRplus assay after positive acid-fast bacilli or culture.
58 d with broth from MGIT cultures positive for acid-fast bacilli or growth on a solid medium, we compar
59 burden, with smear grades scanty or 1+ (1-99 acid-fast bacilli per 100 fields).
60 ious tuberculosis by simple sputum smear for acid-fast bacilli remains an important tool, and more ra
61 phenotypic TB detection tests in the region [acid fast bacilli smear microscopy and Mycobacteria Grow
62 attern, and increase in the highest grade of acid-fast bacilli smear (AFS).
63 erformance scores (P = 0.016), higher sputum acid-fast bacilli smear microscopy grades (P = 0.007), l
64                 We prospectively analyzed 60 acid-fast bacilli smear-positive clinical sputum samples
65                             Patients in whom acid-fast bacilli smear-positive pulmonary tuberculosis
66   Six hundred and fifty-seven direct patient acid-fast bacilli smear-positive specimens resistant to
67 dictor of infection than the standard sputum acid-fast bacilli smear.
68                             Frequency of CSF acid-fast-bacilli smear positivity was 8.9% (95% CI 5.0-
69 is treatment, directly observed therapy, and acid-fast-bacilli smear-positivity to obtain adjusted od
70  Eighty percent (680/848) of patients having acid-fast-bacilli-smear-positive specimens had MTD perfo
71 thological testing of skin-biopsy specimens, acid-fast bacilli smears, and microbial cultures and ant
72  Higher LL-37 concentrations correlated with acid fast bacilli sputum smear positivity and weight gt
73 nosis, 69% of MDR-TB cases were positive for acid-fast bacilli sputum smears and 43% had cavitary dis
74 ne (3%) case of a lymph node with a positive acid-fast bacilli stain.
75  and one necrotizing granuloma (negative for acid-fast bacilli) that grew Mycobacterium kansasii on c
76                   We modified microscopy for acid-fast bacilli to diagnose tuberculosis (TB) using sm
77 ucibacillary specimens that are negative for acid-fast bacilli using smear microscopy.
78        The sensitivity of mSDA for detecting acid-fast bacilli was 96.4% compared to that of MGIT cul
79 ts had acid-fast bacilli detected in smears; acid-fast bacilli were detected in the first submitted s
80                                           No acid-fast bacilli were seen, but small budding yeasts ch
81 red around and within the necrotic core, and acid-fast bacilli were visible both within macrophages a
82 bacteria were found to be classic rod-shaped acid-fast bacilli, while in the stationary phase M. smeg