Sofosbuvir in combination with daclatasvir or simeprevir for 12 weeks in noncirrhotic subjects chronically infected with hepatitis C virus genotype 1: a randomized clinical trial-Reference-Cited by-同舟云学术

Sofosbuvir in combination with daclatasvir or simeprevir for 12 weeks in noncirrhotic subjects chronically infected with hepatitis C virus genotype 1: a randomized clinical trial

Published:2019-03 Issue:3 Volume:25 Page:365-371
ISSN:1198-743X
Container-title:Clinical Microbiology and Infection
language:en
Short-container-title:Clinical Microbiology and Infection

Author:

Pott-Junior H.,Bricks G.,Grandi G.,Figueiredo Senise J.,Castelo Filho A.

Publisher

Elsevier BV

Subject

Infectious Diseases,Microbiology (medical),General Medicine

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4. Daclatasvir plus sofosbuvir, with or without ribavirin, achieved high sustained virological response rates in patients with HCV infection and advanced liver disease in a real-world cohort;Welzel;Gut,2016

5. Safety and efficacy of daclatasvir–sofosbuvir in HCV genotype 1–mono-infected patients;Pol;J Hepatol,2017

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1. SASLT guidelines: Update in treatment of hepatitis C virus infection, 2024;Saudi Journal of Gastroenterology;2024-01

2. Comparative Real Life Egyptian Experience of the Combination of Sofosbuvir Plus Daclatasvir or Simeprevir for 12 Weeks in Naïve Cirrhotic Patients Infected with HCV Genotype 4;Current Drug Safety;2023-05

3. Correlation of host factor with virological response to direct-acting antiviral treatment in hepatitis C patients;Egyptian Liver Journal;2022-09-09

4. A fuzzy logic-based computational method for the repurposing of drugs against COVID-19;BioImpacts;2021-08-10

5. A clinical case of ulcerative colitis in a patient with viral hepatitis;South Russian Journal of Therapeutic Practice;2020-12-20