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1 sions consistent with bacillary angiomatosis-peliosis.
2 stic disease in the liver known as bacillary peliosis.
3 sease, bacillary angiomatosis, and bacillary peliosis.
4 cluding bacillary angiomatosis and bacillary peliosis.
5  the 49 patients with bacillary angiomatosis-peliosis, 26 (53 percent) were infected with B. henselae
6 ered to patients with bacillary angiomatosis-peliosis and to 96 matched controls.
7 servations in cat scratch disease, bacillary peliosis, and bacillary angiomatosis.
8 ver, bacillary angiomatosis, and parenchymal peliosis, and in the case of B. henselae cat-scratch dis
9  lobular inflammation, hepatocyte apoptosis, peliosis, and KC hypertrophy and hyperplasia.
10 ay develop bacillary angiomatosis, bacillary peliosis, and relapsing bacteremia with fever syndrome.
11  including bacillary angiomatosis, bacillary peliosis, and verruga peruana.
12         Bacillary angiomatosis and bacillary peliosis are vascular proliferative manifestations of in
13  organisms that cause bacillary angiomatosis-peliosis, are associated with different epidemiologic ri
14 as bacillary angiomatosis (BA) and bacillary peliosis (BP) in some human hosts.
15 erein, we report the first case of bacillary peliosis hepatis due to systemic Bartonella henselae inf
16                                    Bacillary peliosis hepatis is an uncommon but well recognized dise
17 trongly associated with B. quintana, whereas peliosis hepatis was associated exclusively with B. hens
18 reover, this VEGF-induced syndrome resembles peliosis hepatis, a rare human condition that is encount
19 na; it was also found to cause endocarditis, peliosis hepatis, and bacillary angiomatosis.
20 cat-scratch disease, bacillary angiomatosis, peliosis hepatis, and fever in humans.
21 topathology of the liver biopsy demonstrated peliosis hepatis.

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