コーパス検索結果 (1語後でソート)
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1 he most common clinical pattern was a severe cholestatic hepatitis.
2 those with advanced fibrosis (F3-F4) and/or cholestatic hepatitis.
3 hepatic impairment; and those with fibrosing cholestatic hepatitis.
4 atients with recurrent advanced fibrosis and cholestatic hepatitis.
5 me with growth failure or transient neonatal cholestatic hepatitis.
6 ajor cause of hepatocyte injury in fibrosing cholestatic hepatitis.
7 riants, particularly in those with fibrosing cholestatic hepatitis.
8 P-A, CTP-B, or CTP-C cirrhosis; or fibrosing cholestatic hepatitis.
9 d in 51% with advanced fibrosis and 44% with cholestatic hepatitis.
10 d in 22% with advanced fibrosis and 33% with cholestatic hepatitis.
11 irment, and by all 6 patients with fibrosing cholestatic hepatitis.
13 e patients with advanced fibrosis and 9 with cholestatic hepatitis (74% men, 57% genotype 1a, 63% pre
17 (Mdr2-KO) mice spontaneously develop chronic cholestatic hepatitis and fibrosis that is eventually fo
19 inflammation-mediated HCC, develops chronic cholestatic hepatitis at an early age and HCC at an adul
23 cies may be one mechanism by which fibrosing cholestatic hepatitis develops after liver transplantati
25 hepatitis C, including those with fibrosing cholestatic hepatitis (FCH) and decompensated cirrhosis
29 th early graft failure, similar to fibrosing cholestatic hepatitis seen in some transplant patients w
30 type 1 HCV and advanced fibrosis (F3-4/4) or cholestatic hepatitis treated with telaprevir- or bocepr
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