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1 f the explant (11 alcoholic hepatitis and 33 alcoholic cirrhosis).
2 as being associated with the development of alcoholic cirrhosis.
3 in human alcoholic fatty livers, but not in alcoholic cirrhosis.
4 ents transplanted for a listing diagnosis of alcoholic cirrhosis.
5 oholic fatty liver, alcoholic hepatitis, and alcoholic cirrhosis.
6 s not recommended for patients with advanced alcoholic cirrhosis.
7 ared with placebo, in patients with advanced alcoholic cirrhosis.
8 uccessful in properly selected patients with alcoholic cirrhosis.
9 may occur in severe liver disease including alcoholic cirrhosis.
10 ect on alcohol consumption and its weight on alcoholic cirrhosis.
13 The primary indications for LT listing were alcoholic cirrhosis (9; 27%), nonalcoholic steatohepatit
14 with cryptogenic cirrhosis (CC) (n = 6087), alcoholic cirrhosis (AC) (n = 16 810), and autoimmune he
15 ients with AHC when compared with those with alcoholic cirrhosis (AC) and/or alcoholic hepatitis (AH)
16 vely followed-up cohort of 230 patients with alcoholic cirrhosis (AC) using competing risk analyses.
17 n=3854), hepatitis C virus (HCV; n=15,147), alcoholic cirrhosis (AC; n=8940), HCV+alcohol (n=6066),
18 sed cognitive functions in 117 patients with alcoholic cirrhosis and 163 patients with nonalcoholic c
19 ng candidates for liver transplantation with alcoholic cirrhosis and a persistent sobriety thereafter
21 pressed in a low percentage of patients with alcoholic cirrhosis and do not influence HCC development
22 thanol-treated mice, and human patients with alcoholic cirrhosis and healthy controls were used to qu
24 cytes/macrophages were increased compared to alcoholic cirrhosis and monocytes were found to be locat
25 to determine the mechanisms of sarcopenia in alcoholic cirrhosis and potential reversal by leucine.
27 male patient received a liver transplant for alcoholic cirrhosis and, 6 years later, developed biopsy
28 the explant (46 alcoholic hepatitis and 138 alcoholic cirrhosis) and diagnosis at both listing as we
29 er of early readmission, age > 64 years, non-alcoholic cirrhosis, and length of stay > 10 days were s
30 cytes/macrophages were increased compared to alcoholic cirrhosis, and monocytes were found to be loca
31 is associated with chronic viral infections, alcoholic cirrhosis, and nonalcoholic fatty liver diseas
35 ivariable Cox regression analysis identified alcoholic cirrhosis as etiology of the underlying liver
36 ith NASH and similar to patients with stable alcoholic cirrhosis but not as elevated as in patients w
38 ic kidney disease, type 2 diabetes, gout and alcoholic cirrhosis genetic risk stratification in an in
39 irrhosis, primary sclerosing cholangitis, or alcoholic cirrhosis (group I), NASH, and cryptogenic cir
46 nd-stage liver disease, including those with alcoholic cirrhosis, have normal cardiac function on two
47 , P < 0.001), "substantial" in patients with alcoholic cirrhosis (HR 1.007, P < 0.001), and "rather w
48 13; P < 0.001), substantial in patients with alcoholic cirrhosis (HR, 1.007; P < 0.001) and rather we
49 utophagy in skeletal muscle of patients with alcoholic cirrhosis is acutely reversed by BCAA/LEU.
53 d re-LT for cryptogenic cirrhosis (n = 189), alcoholic cirrhosis (n = 300) or autoimmune hepatitis ci
54 dependent predictor for HCC in patients with alcoholic cirrhosis (odds ratio [OR], 3.2; 95% CI, 1.5-6
55 of liver disease (alcoholic hepatitis versus alcoholic cirrhosis) on the graft and patient survival.
56 ses of liver tissue from patients with AH or alcoholic cirrhosis or normal liver tissue from hepatic
57 ress were assessed in SAH patients (n = 90), alcoholic cirrhosis patients (n = 60), and healthy contr
58 ve protein product) was higher in SAH versus alcoholic cirrhosis patients and healthy controls (P < 0
59 patient survival of alcoholic hepatitis and alcoholic cirrhosis patients were 75% and 73% (P = 0.97)
65 mortality starting 1 year after diagnosis of alcoholic cirrhosis through 2009; ratio of HCC-related m
66 than others (P = 0.03), while patients with alcoholic cirrhosis trended toward worse survival than t
68 coholic liver disease and clinically evident alcoholic cirrhosis (unadjusted OR= 2.25, P=1.7 x 10(-10
69 ar-old man with end-stage liver failure from alcoholic cirrhosis underwent orthotopic liver transplan
70 d RB of PMN from patients with decompensated alcoholic cirrhosis was strongly impaired (30%-35% of co
72 ty-nine patients with advanced (Pugh B or C) alcoholic cirrhosis were randomized to receive either co
76 tis as first liver decompensation (Group 1), alcoholic cirrhosis with >/=6 months abstinence (Group 2
79 uman liver diseases, such as hepatitis C and alcoholic cirrhosis, with an excellent safety profile (b