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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.
8 mycobacterial growth and those with positive acid fast bacilli (AFB) growth were tested to detect myc
9 ns submitted for microscopy for detection of acid-fast bacilli (AFB) and for mycobacterial culture an
15 pic examination of respiratory specimens for acid-fast bacilli (AFB) plays a key role in the initial
16 red to 2 sputum samples, each evaluated with acid-fast bacilli (AFB) smear and mycobacterial culture
17 of tuberculosis (TB) are more accurate than acid-fast bacilli (AFB) smear microscopy and are faster
19 y isolation pending results of serial sputum acid-fast bacilli (AFB) smear microscopy is standard pra
20 farct, adrenal necrosis, and hemorrhage, and acid-fast bacilli (AFB) were seen in the lung, liver, ki
22 ogy, immunohistochemistry (IHC) staining for acid-fast bacilli (AFB), and mycobacterial polymerase ch
23 ure for M. ulcerans, or a smear positive for acid-fast bacilli (AFB), together with a possible histol
27 60 and Middlebrook 7H11 biplates), smear for acid-fast bacilli (AFB; auramine O), and clinical course
28 tions from silica-exposed mice had many more acid fast bacilli(+) (AFB(+)) organisms than from contro
30 agement of highly infectious agents, such as acid-fast bacilli and systemic fungi, were revealed.
31 44 nerves from armadillos were screened for acid-fast bacilli and thin sections were examined ultras
33 ee sputum specimens, which were examined for acid-fast bacilli by use of direct auramine and Ziehl-Ne
36 patients with smears that were positive for acid-fast bacilli had a median treatment interval of 3 d
37 l-defective bacteria which later reverted to acid-fast bacilli have been isolated from sarcoid tissue
38 s included smears of aspirated materials for acid-fast bacilli in 11, mycobacterial culture in 14, an
39 sed on passive case finding and detection of acid-fast bacilli in sputum samples to diagnose pulmonar
40 sure the progressive reduction of numbers of acid-fast bacilli in the sputum smear and the clearance
44 imen inclusion were (i) a positive smear for acid-fast bacilli (n = 54) and (ii) the source if the sm
45 rculosis but sputum smears were negative for acid-fast bacilli on 3 consecutive days) and 22,716 case
47 heterogeneous morphology and distribution of acid-fast bacilli; only at the surface of cavities, i.e.
49 d with broth from MGIT cultures positive for acid-fast bacilli or growth on a solid medium, we compar
50 ious tuberculosis by simple sputum smear for acid-fast bacilli remains an important tool, and more ra
52 erformance scores (P = 0.016), higher sputum acid-fast bacilli smear microscopy grades (P = 0.007), l
54 Six hundred and fifty-seven direct patient acid-fast bacilli smear-positive specimens resistant to
57 Eighty percent (680/848) of patients having acid-fast-bacilli-smear-positive specimens had MTD perfo
58 thological testing of skin-biopsy specimens, acid-fast bacilli smears, and microbial cultures and ant
59 Higher LL-37 concentrations correlated with acid fast bacilli sputum smear positivity and weight gt
61 and one necrotizing granuloma (negative for acid-fast bacilli) that grew Mycobacterium kansasii on c
65 ts had acid-fast bacilli detected in smears; acid-fast bacilli were detected in the first submitted s
67 red around and within the necrotic core, and acid-fast bacilli were visible both within macrophages a
68 bacteria were found to be classic rod-shaped acid-fast bacilli, while in the stationary phase M. smeg
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