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1 nse to peginterferon alpha/ribavirin (PR) in chronic hepatitis C.
2 hly effective for treatment of patients with chronic hepatitis C.
3 f patients with alcohol-related cirrhosis or chronic hepatitis C.
4 n the response to IFN-alpha-based therapy of chronic hepatitis C.
5 g pegIFN-alpha injection in 18 patients with chronic hepatitis C.
6 FN)-induced viral clearance in patients with chronic hepatitis C.
7 ts for prevention of hepatocarcinogenesis in chronic hepatitis C.
8 antiviral responses in patients affected by chronic hepatitis C.
9 on sustained viral response in patients with chronic hepatitis C.
10 nterferon/ribavirin therapy in patients with chronic hepatitis C.
11 hat is likely beneficial in the treatment of chronic hepatitis C.
12 st medical history was notable, however, for chronic hepatitis C.
13 itis B infection and 23 patients (11.2%) had chronic hepatitis C.
14 g its therapeutic potential in patients with chronic hepatitis C.
15 and fibrosis in two cohorts of patients with chronic hepatitis C.
16 USION: FD is more prevalent in patients with chronic hepatitis C.
17 as highlighted by the case of the therapy of chronic hepatitis C.
18 ated with reduced hepcidin expression, e.g., chronic hepatitis C, alcoholic liver disease, or heredit
20 Hepcidin production is often insufficient in chronic hepatitis C and alcoholic liver disease, leading
22 indices of glycemic control in patients with chronic hepatitis C and insulin resistance, but did not
23 onsistent with these findings, patients with chronic hepatitis C and nonalcoholic steatohepatitis sig
24 can capture nonlinear disease progression in chronic hepatitis C and thus outperform baseline models.
25 ng cholangitis, alcoholic liver disease, and chronic hepatitis C), and human cholangiocytes expressed
26 three PIs have been approved for therapy of chronic hepatitis C, and several others are in developme
27 udy, we elucidate the potential link between chronic hepatitis C-associated inflammation and alterati
28 ially studied and validated in patients with chronic hepatitis C but are now used increasingly for pa
30 known whether chronic hepatitis B (CH-B) or chronic hepatitis C (CH-C) carries a greater risk of liv
31 ] allele is more represented in HCC cases in chronic hepatitis C (CHC) and alcoholic liver disease (A
32 131 HCC patients, 76 cirrhosis patients, 52 chronic hepatitis C (CHC) and B (CHB) patients, and 53 h
33 Most of these markers have been developed in chronic hepatitis C (CHC) and nonalcoholic fatty liver d
35 FLD and liver damage progression in NASH and chronic hepatitis C (CHC) by still undefined mechanisms,
37 mproving prediction of treatment outcomes in chronic hepatitis C (CHC) genotype 4 (G4) is necessary t
43 he severity of liver disease associated with chronic hepatitis C (CHC) on healthcare costs has not be
45 (TVR)-based TT in untreated genotype 1 (G1) chronic hepatitis C (CHC) patients discriminated accordi
47 se (ALT) elevation and associated factors in chronic hepatitis C (CHC) patients who achieved undetect
51 pe of hepatitis C virus (HCV) treatment, but chronic hepatitis C (CHC) remains a leading indication f
52 latelet count < 50,000/muL) in patients with chronic hepatitis C (CHC) undergoing antiviral therapy,
53 about mortality rates (MRs) in patients with chronic hepatitis C (CHC) with cirrhosis is limited.
54 hort of 4,172 patients, including 3,129 with chronic hepatitis C (CHC), 555 with chronic hepatitis B
55 nic course: n = 17), 12 HIV(+) patients with chronic hepatitis C (CHC), 8 HIV monoinfected individual
56 ith confirmed early PBC, 10 with early stage chronic hepatitis C (CHC), and nine with resolving, self
58 assess the accuracy of SWE in patients with chronic hepatitis C (CHC), in comparison with transient
59 epatitis C virus (HCV) is a leading cause of chronic hepatitis C (CHC), liver cirrhosis, and hepatoce
60 t hepatitis C virus (HCV) infection leads to chronic hepatitis C (CHC), which often progresses to liv
73 allenges include increasing awareness of the chronic hepatitis C epidemic, garnering sufficient publi
75 e inhibitors as part of standard therapy for chronic hepatitis C genotype 1 infection, drug-drug inte
76 m 640 Japanese patients who were treated for chronic hepatitis C genotype 1, 2, or 3 with pegylated i
81 terferon (PEG-IFN)-alpha in the treatment of chronic hepatitis C has led to an increase in sustained
85 A new standard of care for the treatment of Chronic Hepatitis C (HCV) emerged in 2011 with the appro
86 pproved for response-guided-therapy (RGT) of chronic hepatitis C (HCV) genotype-1-infection in treatm
87 f Ledipasvir/Sofosbuvir for the treatment of chronic hepatitis C (HCV) includes the truncation of the
92 liver damage, especially in individuals with chronic hepatitis C (HCV); however, the impact of nonhea
94 the management of acute infectious diseases, chronic hepatitis C, human immunodeficiency virus, and a
96 ession analysis, methadone doses (P = .005), chronic hepatitis C-induced cirrhosis (P = .008), and be
97 ors for prolongation of the QTc interval are chronic hepatitis C-induced cirrhosis, higher methadone
98 the past decade, the standard treatment for chronic hepatitis C infection has been pegylated-interfe
99 Compared with other countries, patients with chronic hepatitis C infection in Japan tend to be older,
101 of hepatitis and fibrosis progression during chronic hepatitis C infection, while contrasting results
106 nterferon-free regimens for the treatment of chronic hepatitis C infections needs to be evaluated in
108 study suggests that the long-term course of chronic hepatitis C is determined early in infection and
110 erexpression of FBP1 in most HCC tumors with chronic hepatitis C is significantly linked with the dec
113 ymorphisms at ITPA and treatment efficacy in chronic hepatitis C mediated by reduced relapse risk.
114 ame organ (liver) derived from patients with chronic hepatitis C: On the one side, cirrhotic and tumo
115 mbined cohort of non-cirrhotic patients with chronic hepatitis C or alcoholic liver disease (n = 1121
124 appears to affect early VKs in patients with chronic hepatitis C receiving interferon-free treatment.
126 n-free, direct-acting antiviral treatment of chronic hepatitis C, subjects who received ribavirin had
127 t has recently been applied to patients with chronic hepatitis C, successfully clearing hepatitis C v
129 notype affects the response of patients with chronic hepatitis C to peginterferon and ribavirin, litt
130 owledge, none of the studies of vitamin D in chronic hepatitis C treatment have included a significan
131 een the 25(OH)D concentration and genotype 1 chronic hepatitis C treatment response in African Americ
136 y activity and fibrosis in 551 patients with chronic hepatitis C virus (HCV) and 203 patients with ch
139 ring nonalcoholic steatohepatitis (NASH) and chronic hepatitis C virus (HCV) compared to alcohol live
140 for 24 weeks was recently approved to treat chronic hepatitis C virus (HCV) genotype 1 (GT-1) infect
141 proved in the United States for treatment of chronic hepatitis C virus (HCV) genotype 1 and 4 infecti
142 proved in the United States for treatment of chronic hepatitis C virus (HCV) genotype 1 and 4 infecti
143 hase 3 study in previous non-responders with chronic hepatitis C virus (HCV) genotype 1 infection and
145 telaprevir in treatment-naive patients with chronic hepatitis C virus (HCV) genotype 1 infection, in
146 virin in treatment-experienced patients with chronic hepatitis C virus (HCV) genotype 1 infection.
147 ogical response (SVR) rates in patients with chronic hepatitis C virus (HCV) genotype 1 infections, b
148 virin (RBV) in treatment-naive patients with chronic hepatitis C virus (HCV) genotype 1 without cirrh
149 ective in previously untreated patients with chronic hepatitis C virus (HCV) genotype 1, 2, or 3 infe
150 tions are rapidly evolving for patients with chronic hepatitis C virus (HCV) genotype 1b (GT1b) infec
152 eatment with peginterferon and ribavirin for chronic hepatitis C virus (HCV) genotype 2 or 3 infectio
153 ermine the optimal regimen for patients with chronic hepatitis C virus (HCV) genotype 2, 3, 4, or 6 i
154 ed regimens in treatment-naive patients with chronic hepatitis C virus (HCV) genotype 4 infection.
155 ear, the landscape of therapy for genotype 1 chronic hepatitis C virus (HCV) has changed dramatically
157 nomic burden imposed by the complications of chronic hepatitis C virus (HCV) infection - including ci
158 rect-acting antiviral agents that can cure a chronic hepatitis C virus (HCV) infection after 8-12 wee
161 ng evidence indicates an association between chronic hepatitis C virus (HCV) infection and B-cell lym
162 ns are needed for treatment of patients with chronic hepatitis C virus (HCV) infection and cirrhosis.
163 previr regimen for 12 weeks in patients with chronic hepatitis C virus (HCV) infection and stage 4-5
164 ole of MAIT cells in livers of patients with chronic hepatitis C virus (HCV) infection and their fate
166 trials have demonstrated that patients with chronic hepatitis C virus (HCV) infection associated HCC
170 ons in the peripheral blood of patients with chronic hepatitis C virus (HCV) infection compared to su
171 An unbiased genome-to-genome analysis in chronic hepatitis C virus (HCV) infection confirms the i
173 d neurocognitive impairment in patients with chronic hepatitis C virus (HCV) infection even before li
174 eron-alpha (IFNalpha) has been used to treat chronic hepatitis C virus (HCV) infection for over 20 ye
179 direct-acting antiviral (DAA) therapies for chronic hepatitis C virus (HCV) infection have demonstra
181 Use of interferon and ribavirin to treat chronic hepatitis C virus (HCV) infection in kidney tran
182 nd: Use of interferon and ribavirin to treat chronic hepatitis C virus (HCV) infection in kidney tran
183 interferon- and ribavirin-free treatment for chronic hepatitis C virus (HCV) infection in patients co
185 to improve access to care and treatment for chronic hepatitis C virus (HCV) infection in resource-li
191 , interferon-alpha (IFN-alpha) treatment for chronic hepatitis C virus (HCV) infection is an ideal mo
194 A key question in care of patients with chronic hepatitis C virus (HCV) infection is beginning t
202 and ribavirin (IFN-alpha/RBV) treatment for chronic hepatitis C virus (HCV) infection is influenced
206 of liver disease in untreated children with chronic hepatitis C virus (HCV) infection is poorly docu
208 e status in liver and blood of patients with chronic hepatitis C virus (HCV) infection long after the
209 th human immunodeficiency virus (HIV) and/or chronic hepatitis C virus (HCV) infection may be prescri
212 ere are no effective and safe treatments for chronic hepatitis C virus (HCV) infection of patients wh
215 eprevir- and telaprevir-based treatments for chronic hepatitis C virus (HCV) infection use specific r
216 increases treatment efficacy for genotype 1 chronic hepatitis C virus (HCV) infection versus PEG-IFN
220 is a major complication during treatment of chronic hepatitis C virus (HCV) infection with interfero
221 ee, complete regimen for adult patients with chronic hepatitis C virus (HCV) infection without cirrho
223 ting antivirals (DAAs) effectively eradicate chronic hepatitis C virus (HCV) infection, although HCV
225 have recently been approved for treatment of chronic hepatitis C virus (HCV) infection, are more effi
226 inistration to treat persons with genotype 1 chronic hepatitis C virus (HCV) infection, but not those
227 to a high cure rate in treated patients with chronic hepatitis C virus (HCV) infection, but this stil
228 d with clinical and histological features of chronic hepatitis C virus (HCV) infection, including nec
229 nterferon and ribavirin for the treatment of chronic hepatitis C virus (HCV) infection, increase the
230 course of direct-acting antiviral agents for chronic hepatitis C virus (HCV) infection, we examined t
231 ent standard of care combination therapy for chronic hepatitis C virus (HCV) infection, yet the compo
254 e natural history and treatment responses of chronic hepatitis C virus (HCV) infection; however, dist
257 nterferon-free regimens for the treatment of chronic hepatitis C virus (HCV) infections require furth
258 The evolution of treatment for patients with chronic hepatitis C virus (HCV) is evolving at a rapid p
259 e direct-acting antivirals (DAA) in treating chronic hepatitis C virus (HCV) is limited by low screen
260 The global burden of disease attributable to chronic hepatitis C virus (HCV) is very large, yet the u
261 1 healthy individuals (NC) (n = 20), group 2 chronic hepatitis C virus (HCV) patients (n = 20), group
265 ntibodies (FPAs) have been well described in chronic hepatitis C virus (HCV), this has not been evalu
266 the risk of chronic kidney disease (CKD) in chronic hepatitis C virus (HCV)-infected patients and th
274 evir + TMC647055/ritonavir + JNJ-56914845 in chronic hepatitis C virus genotype (GT)1-infected treatm
276 afe and highly effective in adolescents with chronic hepatitis C virus genotype 2 or 3 infection.
277 ns with or without ribavirin as treatment of chronic hepatitis C virus in solid organ transplant reci
281 -acting antiviral drugs for the treatment of chronic hepatitis C virus infection have reduced mortali
282 pulations after DAA therapy in patients with chronic hepatitis C virus infection in the context of th
285 ffective and well tolerated in patients with chronic hepatitis C virus infection, including those wit
286 nse (SVR) to interferon-based treatments for chronic hepatitis C virus infection, whereas Asian race
291 iling the response to interferon therapy (in chronic Hepatitis C virus patients) and Influenza A viru
292 le degree of liver fibrosis in patients with chronic hepatitis C virus prohibiting cadaveric renal tr
293 acting antiviral agents for the treatment of chronic hepatitis C virus that have significantly increa
295 lular carcinoma was overrepresented, whereas chronic hepatitis C was underrepresented, in reported Un
296 ting new direct-acting antivirals (DAAs) for chronic hepatitis C were the major focus of interest at
297 This represents a major difference from chronic hepatitis C, where numerous previous studies hav
299 To address this issue, 126 patients with chronic hepatitis C who completed pegylated IFN plus rib
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