Objectives: This study aimed to investigate the effect of treatment with direct-acting antivirals (DAAs) on the virological response and on the some parameters used to evaluate liver function in cases with chronic liver disease due to hepatitis C virus (HCV) genotype 1b. Materials and Methods: This study included cases who were treated with DAAs after HCV genotype 1b infection. HCV-RNA levels and biochemical and hematological parameters measured at the beginning of treatment, 12th week and 52th week after the treatment were transferred to the SPSS statistics software. model for end-stage liver disease (MELD) and Child-Pugh scores were also calculated and added to these data. Results: The study group consisted of a total of 102 patients, inc...
BACKGROUND & AIMS: Patients with chronic hepatitis C virus (HCV) infection and cirrhosis have a high...
AIM : To assesse the efficacy and safety of therapy with daclatasvir (DCV) and asunaprevir (ASV) for...
Background and objectives: this study assessed variations in the blood parameters of patients with h...
Aim of study: To evaluate results of direct acting antiviral therapy for chronic hepatitis C in LUHS...
Aim: The aim was to assess the clinical impact of direct-acting antiviral treatment in patients with...
AIM: To study the outcomes of patients with compensated hepatitis C virus-related cirrhosis. METHODS...
Background & Aims: All oral direct acting antivirals (DAAs) effectively treat chronic hepati...
Background: The efficacy and safety of asunaprevir + daclatasvir combination therapy for treatment o...
AbstractBackground: All oral direct-acting antivirals (DAAs) effectively treat chronic hepatitis C i...
Background and Aims: All oral direct-acting antivirals (DAAs) effectively treat chronic hepatitis C ...
BACKGROUND:Hepatitis C virus (HCV) infection is the major cause of end-stage liver disease (LD) worl...
Objective: To evaluate the efficacy of sofosbuvir with daclatasvir and its promising effects on live...
Safety, efficacy, and predictor factors of sustained-virological-response after 24 weeks of new dire...
Chronic hepatitis C virus (HCV) infection could ultimately trigger liver cirrhosis (LC), an ailment ...
Aim of the study. To estimate efficacy and safety of 3D mode of interferonfree therapy in patients ...
BACKGROUND & AIMS: Patients with chronic hepatitis C virus (HCV) infection and cirrhosis have a high...
AIM : To assesse the efficacy and safety of therapy with daclatasvir (DCV) and asunaprevir (ASV) for...
Background and objectives: this study assessed variations in the blood parameters of patients with h...
Aim of study: To evaluate results of direct acting antiviral therapy for chronic hepatitis C in LUHS...
Aim: The aim was to assess the clinical impact of direct-acting antiviral treatment in patients with...
AIM: To study the outcomes of patients with compensated hepatitis C virus-related cirrhosis. METHODS...
Background & Aims: All oral direct acting antivirals (DAAs) effectively treat chronic hepati...
Background: The efficacy and safety of asunaprevir + daclatasvir combination therapy for treatment o...
AbstractBackground: All oral direct-acting antivirals (DAAs) effectively treat chronic hepatitis C i...
Background and Aims: All oral direct-acting antivirals (DAAs) effectively treat chronic hepatitis C ...
BACKGROUND:Hepatitis C virus (HCV) infection is the major cause of end-stage liver disease (LD) worl...
Objective: To evaluate the efficacy of sofosbuvir with daclatasvir and its promising effects on live...
Safety, efficacy, and predictor factors of sustained-virological-response after 24 weeks of new dire...
Chronic hepatitis C virus (HCV) infection could ultimately trigger liver cirrhosis (LC), an ailment ...
Aim of the study. To estimate efficacy and safety of 3D mode of interferonfree therapy in patients ...
BACKGROUND & AIMS: Patients with chronic hepatitis C virus (HCV) infection and cirrhosis have a high...
AIM : To assesse the efficacy and safety of therapy with daclatasvir (DCV) and asunaprevir (ASV) for...
Background and objectives: this study assessed variations in the blood parameters of patients with h...