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1 ct analysis" OR "cost benefit analysis" AND "hepatitis C".
2 revention of hepatocarcinogenesis in chronic hepatitis C.
3 by deadly RNA viruses such as influenza, and Hepatitis C.
4 US West and South have been most impacted by hepatitis C.
5 infections (eg, highest reported was 90% for hepatitis C, 67 [65%] of 103 individuals for hepatitis B
7 r racial groups show increasing rates due to hepatitis C and emergence of cirrhosis from non-alcoholi
9 ition has been a target for the treatment of hepatitis C and other diseases, but the generation of po
14 Hepatology practice has been dominated by hepatitis C but is now being overtaken by patients with
19 patitis C virus (HCV) treatment, but chronic hepatitis C (CHC) remains a leading indication for liver
21 th better clinical outcomes in patients with hepatitis C cirrhosis (n = 216), suggesting it may have
24 ents if they were hepatitis B-co-infected or hepatitis C-co-infected, had new AIDS-defining condition
27 nt prevalence of HIV, hepatitis B (HBV), and hepatitis C (HCV) in people with severe mental illness,
30 a quarter of individuals clear their primary hepatitis C (HCV) infections spontaneously, clearance (s
31 mage, especially in individuals with chronic hepatitis C (HCV); however, the impact of nonheavy use i
32 hronic liver diseases (CLDs), due to chronic hepatitis C; hepatitis B; nonalcoholic fatty liver disea
33 (HR, 15.9; 95% CI 1.8-145.2), and recipient hepatitis C (HR, 5.5; 95% CI 1.7-17.8) were significant
34 ation after DAA-based treatment of recurrent hepatitis C in an antibody against hepatitis B core anti
35 this Series paper, several issues related to hepatitis C in sub-Saharan Africa are addressed, includi
37 uture CHF events, particularly among HIV and hepatitis C infected people among whom cardiovascular di
40 itis and fibrosis progression during chronic hepatitis C infection, while contrasting results were re
46 ohort of non-cirrhotic patients with chronic hepatitis C or alcoholic liver disease (n = 1121), the T
49 terferon (IFN)-alpha treated chimpanzees and hepatitis C patients showed elevated APOBEC expression.
51 vational studies among compensated cirrhotic hepatitis C patients treated with interferon-containing
52 infected patients with deep vein thrombosis, hepatitis C, renal impairment, thyroid disease, and live
54 luation to Advance Screening and Testing for Hepatitis C study on HCV testing and costs among persons
55 kidney (DLK) transplant recipients from the Hepatitis C Therapeutic Registry and Research Network da
56 ses of acute symptomatic HEV infection after hepatitis C therapy in patients carrying anti-HEV immuno
57 and in this era of safer and more effective hepatitis C therapy, non-alcoholic fatty liver disease (
60 icant cardiovascular disease, hepatitis B or hepatitis C viral infection, and a known bleeding disord
66 steatosis (HS) is common in individuals with hepatitis C virus (HCV) and human immunodeficiency virus
67 Patients who are chronically infected with hepatitis C virus (HCV) and who do not have a sustained
68 [BPA], and patient solicitation), evaluated hepatitis C virus (HCV) antibody testing, diagnosis, and
69 afety and efficacy in treating patients with hepatitis C virus (HCV) awaiting liver transplant (LT).
72 urrent standard of care for the treatment of hepatitis C virus (HCV) consists of interferon-free dire
75 we longitudinally sampled and sequenced the hepatitis C virus (HCV) envelope genome region (1,680 nu
81 S5A, which is involved in replication of the hepatitis C virus (HCV) genome, presumably via membranou
82 r + DSV) +/- ribavirin (RBV) is approved for hepatitis C virus (HCV) genotype 1 (GT1) treatment in HI
83 n the United States for treatment of chronic hepatitis C virus (HCV) genotype 1 and 4 infections, as
85 BACKGROUND & AIMS: Patients with chronic hepatitis C virus (HCV) genotype 2 have high rates of re
90 is study examined the interactions among the hepatitis C virus (HCV) helicase and RLR helicases in li
92 changes that occur upon prolonged passage of hepatitis C virus (HCV) in human hepatoma cells in an ex
93 tly-acting antivirals has been advocated for Hepatitis C Virus (HCV) in people who inject drugs (PWID
94 dynamics, and phenotypic diversification of hepatitis C virus (HCV) in the course of 200 passages in
96 recommended regimens to treat patients with hepatitis C virus (HCV) infection after liver transplant
98 known of an epidemic of sexually transmitted hepatitis C virus (HCV) infection among human immunodefi
99 response (SVR) on outcomes of patients with hepatitis C virus (HCV) infection and compensated cirrho
100 lecaprevir and pibrentasvir in patients with hepatitis C virus (HCV) infection and compensated cirrho
102 egimen for 12 weeks in patients with chronic hepatitis C virus (HCV) infection and stage 4-5 chronic
103 ociations between hepatitis B virus (HBV) or hepatitis C virus (HCV) infection and the development of
104 AIT cells in livers of patients with chronic hepatitis C virus (HCV) infection and their fate after a
106 pment of drugs targeting the early stages of Hepatitis C virus (HCV) infection are hampered by the la
107 tive studies of the outcomes associated with hepatitis C virus (HCV) infection are rare and critical
108 have demonstrated that patients with chronic hepatitis C virus (HCV) infection associated HCC survive
109 nbiased genome-to-genome analysis in chronic hepatitis C virus (HCV) infection confirms the innate an
111 with persistent and spontaneously resolving hepatitis C virus (HCV) infection during the acute phase
114 Direct-acting antiviral (DAA) therapy for hepatitis C virus (HCV) infection has resulted in high r
115 acting antiviral (DAA) therapies for chronic hepatitis C virus (HCV) infection have demonstrated high
116 BACKGROUND & AIMS: Patients with chronic hepatitis C virus (HCV) infection have high rates of sus
117 of interferon and ribavirin to treat chronic hepatitis C virus (HCV) infection in kidney transplant r
118 ffective, and pan-genotypic regimen to treat hepatitis C virus (HCV) infection in patients coinfected
119 ng antiviral (DAA) medications, treatment of hepatitis C virus (HCV) infection in renal transplant re
120 asvir-sofosbuvir is effective at eradicating hepatitis C virus (HCV) infection in the general populat
121 In a previous study, we have shown that hepatitis C virus (HCV) infection induces epithelial-mes
128 efficacy of antiviral treatment for chronic hepatitis C virus (HCV) infection is determined by measu
132 immunodeficiency virus (HIV) and/or chronic hepatitis C virus (HCV) infection may be prescribed stat
133 s stage influences the CHF risk or if HIV or hepatitis C virus (HCV) infection modifies this associat
134 Whether chronic hepatitis B virus (HBV) and hepatitis C virus (HCV) infection promote NHL in HIV-inf
135 lines now recommend that patients with acute hepatitis C virus (HCV) infection should be treated with
136 e the relationships of hepatitis B (HBV) and hepatitis C virus (HCV) infection to age-related catarac
138 atocellular carcinoma (HCC) in patients with hepatitis C virus (HCV) infection treated with direct-ac
141 lete regimen for adult patients with chronic hepatitis C virus (HCV) infection without cirrhosis or w
143 ins are detected in 40%-60% of patients with hepatitis C virus (HCV) infection, and overt cryoglobuli
144 e the availability of curative treatment for hepatitis C virus (HCV) infection, because of cost, trea
145 ptor proteins AP1 and AP2, are essential for hepatitis C virus (HCV) infection, but the underlying me
147 ent of more effective drugs for treatment of hepatitis C virus (HCV) infection, there has been an inc
154 artments (EDs) seem to be able to detect new hepatitis C virus (HCV) infections at a high rate, but i
158 itious targets for global control of HIV and hepatitis C virus (HCV) is low levels of awareness of in
164 formed by glycoproteins E1 and E2 within the hepatitis C virus (HCV) lipid envelope is a potential va
166 nt pan-genotype and macrocyclic inhibitor of hepatitis C virus (HCV) NS3/4A protease and was develope
169 enib with alternative therapies according to hepatitis C virus (HCV) or hepatitis B virus (HBV) statu
170 rotein synthesis to directly incorporate the hepatitis C virus (HCV) p7 protein into supported lipid
171 s an urgent need for a vaccine to combat the hepatitis C virus (HCV) pandemic, and induction of broad
172 rd-of-care treatment of chronically infected hepatitis C virus (HCV) patients involves direct-acting
174 to assess human immunodeficiency virus (HIV)/hepatitis C virus (HCV) real-world treatment outcomes.
175 pite recent advances in therapeutic options, hepatitis C virus (HCV) remains a severe global disease
177 , exhibit potent inhibitory activity against hepatitis C virus (HCV) replication in genotype 1b Con 1
181 polymerase that catalyzes replication of the hepatitis C virus (HCV) RNA genome and therefore is cent
182 The affordable and reliable detection of Hepatitis C Virus (HCV) RNA is a cornerstone in the mana
184 an electronic health record-based prompt on hepatitis C virus (HCV) screening rates in baby boomers
185 ntive Services Task Force recommend one-time hepatitis C virus (HCV) testing for persons born during
189 out substitutions that mediate resistance of hepatitis C virus (HCV) to direct-acting antivirals (DAA
191 ivirals (DAAs) have changed the landscape of hepatitis C virus (HCV) treatment, but chronic hepatitis
195 ect drugs (PWID); and the prevalence of HIV, hepatitis C virus (HCV), and hepatitis B virus (HBV) amo
196 for detection of cirrhosis in patients with hepatitis C virus (HCV), hepatitis B virus (HBV), NAFLD,
197 th decompensated cirrhosis (DC) secondary to hepatitis C virus (HCV), is associated with improved hep
198 RNA (+RNA) viruses including human pathogens hepatitis C virus (HCV), Severe acute respiratory syndro
199 with human immunodeficiency virus (HIV) and hepatitis C virus (HCV), we assessed fibrosis progressio
200 cohort of human immunodeficiency virus (HIV)/hepatitis C virus (HCV)-coinfected patients treated with
201 was cloned from T cells that expanded when a hepatitis C virus (HCV)-infected HLA-A2(-) individual re
202 k of chronic kidney disease (CKD) in chronic hepatitis C virus (HCV)-infected patients and the incide
209 Guidelines recommend that patients with hepatitis C virus (HCV)-related liver disease be treated
219 ly observed in individuals infected with the hepatitis C virus (HCV); however, the underlying molecul
221 igh rates of sustained virological response (hepatitis C virus [HCV] RNA <15 IU/mL) at post-treatment
222 serostatus (+ or -: hepatitis B core [HBc], hepatitis C virus [HCV], Epstein-Barr virus [EBV], or cy
223 a performed well in patients with cACLD with hepatitis C virus and alcoholic and nonalcoholic steatoh
224 We demonstrate that, in sharp contrast to hepatitis C virus and human immunodeficiency virus patie
226 or ultrasensitive and selective detection of hepatitis C virus core antigen (HCV) have been investiga
228 MC647055/ritonavir + JNJ-56914845 in chronic hepatitis C virus genotype (GT)1-infected treatment-naiv
234 caprevir/pibrentasvir (G/P) in patients with hepatitis C virus genotype 3 infection with prior treatm
235 or without ribavirin as treatment of chronic hepatitis C virus in solid organ transplant recipients a
236 n (54.1%, P = 0.001), had lower incidence of hepatitis C virus infection (4.9%, P = 0.001) and longer
237 old-especially those born in the peak era of hepatitis C virus infection and among whites/Caucasians.
238 called mixed cryoglobulinemia and is seen in hepatitis C virus infection and systemic diseases such a
240 antiviral drugs for the treatment of chronic hepatitis C virus infection have reduced mortality and t
241 s after DAA therapy in patients with chronic hepatitis C virus infection in the context of the immune
244 report a case series of three patients with hepatitis C virus infection who all presented with sever
245 djusted for age, race or ethnicity, smoking, hepatitis C virus infection, alcohol use disorders, drug
246 and well tolerated in patients with chronic hepatitis C virus infection, including those with compen
247 ) to interferon-based treatments for chronic hepatitis C virus infection, whereas Asian race was asso
250 us infection; 29.1% (95% CI: 23.6-34.5%) for hepatitis C virus infection; 33.9% (95% CI: 24.3-43.5%)
251 through the control of hepatitis B virus and hepatitis C virus infections by vaccination and treatmen
253 ture-based design of HCV vaccines.IMPORTANCE Hepatitis C virus is a leading cause of liver disease an
255 stimulation during persistent infection with hepatitis C virus is associated with continuous activati
257 listed women differed in age (58 vs 57), non-hepatitis C virus listing diagnoses (69% vs 56%), hepati
258 29382 young persons currently infected with hepatitis C virus lived >10 miles from a syringe service
259 avage of four novel substrate motifs for the hepatitis C virus NS3/4 protease using an in vivo assay.
260 We conducted a retrospective cohort study of hepatitis C virus patients who were treated with DAA in
262 th cold ischemic time >12 hours, livers from hepatitis C virus positive donors, livers from donation
264 ssion, all from an active IVDU donor who was hepatitis C virus seronegative at time of donation, but
265 ify the transmission dynamics that drive the hepatitis C virus subtypes 4a (HCV4a) and 4d (HCV4d) epi
267 nce of some countries not following the 2016 hepatitis C virus treatment guidelines by the European A
268 rejection (n = 2 KT, 4 LT) occurred, during hepatitis C virus treatment in 4 and after cessation of
271 ategy for patients chronically infected with hepatitis C virus who experience virologic failure after
273 ople have been estimated to be infected with hepatitis C virus, and many more are at risk for infecti
274 a from patients with AIH, hepatitis B virus, hepatitis C virus, and nonalcoholic steatohepatitis.
275 SV) 1 and 2, human immunodeficiency virus 1, hepatitis C virus, enterovirus 70, and variant Creutzfel
276 st a wide variety of viruses, including HIV, hepatitis C virus, hepatitis B virus, enterovirus 71, in
277 as well as profound antiviral effect against hepatitis C virus, human rhinovirus, and coxsackievirus
278 ood and tissue donors, persons infected with hepatitis C virus, persons with elevated alanine aminotr
279 involved in the assembly and release of the hepatitis C virus, was determined from proteins expresse
280 the setting of viral hepatitis, particularly hepatitis C virus, where sustained viral response has be
281 ral direct-acting antiviral drugs (DAAs) for hepatitis C virus, which have response rates of 95% or m
283 enter prospective study of 226 patients with hepatitis C virus-associated cirrhosis and CSPH who had
284 AA) therapies are effective in patients with hepatitis C virus-induced cryoglobulinemia vasculitis (H
285 hepatitis B virus (HBV) has been reported in hepatitis C virus-infected individuals receiving direct-
288 ir (LDV/SOF) can be considered in genotype 1 hepatitis C virus-infected patients who are treatment-na
289 treatment policies in a real-life cohort of hepatitis C virus-infected policy 1, "universal," treat
290 his retrospective evaluation included 62,290 hepatitis C virus-infected veterans completing oral DAA
295 further show that kinesin knockdown inhibits hepatitis-C virus replication in hepatocytes, likely bec
297 ory and immunosuppressive medication against hepatitis C was the key reason for the good results in t
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