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1 rsity and consisted almost exclusively of M. gordonae.
2 e additional culture that grew Mycobacterium gordonae.
3 with M. kansasii, and 0% of patients with M. gordonae.
4 7) for M. kansasii, and 26% (9 of 35) for M. gordonae.
5 were identified as M. terrae complex and M. gordonae.
6 scofulaceum, M. phlei, M. smegmatis, and M. gordonae.
9 utoff was lowered to 10,000 RLU, 67 of 71 M. gordonae (94.4%) and 32 of 34 M. avium complex (94.1%) s
10 ottles from clinical specimens containing M. gordonae and 34 containing M. avium, confirmed by cultur
11 , San Diego, Calif.) to detect Mycobacterium gordonae and Mycobacterium avium complex directly in liq
12 intracellulare complex, 3 M. kansasii, 4 M. gordonae, and 5 M. chelonae group (all were M. abscessus
13 low growers like M. kansasii, M. szulgai, M. gordonae, and M. asiaticum; however, in these samples, r
17 The BACTEC 460 and the MB/BacT detected M. gordonae in four specimens, but only a single specimen w
19 uding Mycobacterium smegmatis, Mycobacterium gordonae, Mycobacterium chelonae, Mycobacterium fortuitu
20 aining Mycobacterium abscessus,Mycobacterium gordonae, o rMycobacterium thermoresistibile In the clin
21 r determining a positive result using the M. gordonae or M. avium complex probes when testing instrum
22 cimens shown by culture to contain either M. gordonae or M. avium complex tested positive with the pr
23 nsions containing M. avium, M. fortuitum, M. gordonae, or M. marinum incubated with various concentra
26 terium tuberculosis, M. avium complex, or M. gordonae showed that 87% were identified by direct testi
27 ificity was 100% for specimens containing M. gordonae that were tested with the M. avium complex prob
28 ignificantly longer, the recovery rate of M. gordonae was significantly higher, and the number of fal
29 ff, 55 of 71 (77.5%) specimens containing M. gordonae yielded positive results, whereas 28 of 34 (82.