Icaritin delays CCl4-induced hepatic cirrhosis in rats by protecting hepatocytes from oxidative injury

2011 ◽  
Vol 31 (6) ◽  
pp. 625-629 ◽  
Author(s):  
Hai-hua QIAN ◽  
Peng LIU ◽  
Jing LI ◽  
Lei CHEN ◽  
Lu CAO ◽  
...  
2001 ◽  
Vol 120 (5) ◽  
pp. A2-A2
Author(s):  
G FELICIANGELI ◽  
G ARGALIA ◽  
L BOLOGNINI ◽  
T ABBATTISTA ◽  
M URBANI ◽  
...  

2001 ◽  
Vol 120 (5) ◽  
pp. A152-A152
Author(s):  
H SUZUKI ◽  
S NAGAHASHI ◽  
M MIYAZAWA ◽  
M MORI ◽  
H NAGATA ◽  
...  

1955 ◽  
Vol 29 (2) ◽  
pp. 258-261 ◽  
Author(s):  
Dennis A.J. Morey ◽  
James O. Burke

1961 ◽  
Vol 40 (3) ◽  
pp. 389-396 ◽  
Author(s):  
John Laidlaw ◽  
A.E. Read ◽  
Sheila Sherlock

Infectio ro ◽  
2017 ◽  
Vol 3 (51) ◽  
Author(s):  
Gabriela-Loredana Popa ◽  
Silvana-Adelina Gheorghe ◽  
Mădălina Preda

2012 ◽  
pp. 107-113
Author(s):  
Van Huy Tran ◽  
Hoai Phong Nguyen

Background: The recent studies concerning antiviral therapy in HBV-related cirrhosis showed the promising results. This study is aimed at assessing efficacy of lamivudine in patients with HBV-related cirrhosis. Patients and methods: 41 patients with HBsAg positive-cirrhosis and evidence of viral replication were enrolled in the study. Lamivudine is given 100 mg per day and the follow-up is 12 months. Results: The rates of HBV DNA undetectable was 58.53%, 68.29% and 87.80% after 36.6 and 12 months, respectively. The rate of HBeAg loss and HBeAg seroconversion are 57.14% and 35.71%. Child-Pugh scores decreased significantly after 6 and 12 months. The complications of cirrhosis were infrequent. Conclusion: Lamivudine appeared effective and safe in HBV-related hepatic cirrhosis.


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