コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 and fibrosis in two cohorts of patients with chronic hepatitis C.
2 USION: FD is more prevalent in patients with chronic hepatitis C.
3 as highlighted by the case of the therapy of chronic hepatitis C.
4 and averted 252 (134-389) deaths related to chronic hepatitis C.
5 nse to peginterferon alpha/ribavirin (PR) in chronic hepatitis C.
6 hly effective for treatment of patients with chronic hepatitis C.
7 f patients with alcohol-related cirrhosis or chronic hepatitis C.
8 n the response to IFN-alpha-based therapy of chronic hepatitis C.
9 g pegIFN-alpha injection in 18 patients with chronic hepatitis C.
10 FN)-induced viral clearance in patients with chronic hepatitis C.
11 antiviral responses in patients affected by chronic hepatitis C.
12 on sustained viral response in patients with chronic hepatitis C.
13 s patient-reported outcomes in patients with chronic hepatitis C.
14 ts for prevention of hepatocarcinogenesis in chronic hepatitis C.
15 nt scale-up, which has reduced the burden of chronic hepatitis C.
17 ated with reduced hepcidin expression, e.g., chronic hepatitis C, alcoholic liver disease, or heredit
19 onsistent with these findings, patients with chronic hepatitis C and nonalcoholic steatohepatitis sig
20 can capture nonlinear disease progression in chronic hepatitis C and thus outperform baseline models.
21 ng cholangitis, alcoholic liver disease, and chronic hepatitis C), and human cholangiocytes expressed
22 three PIs have been approved for therapy of chronic hepatitis C, and several others are in developme
23 udy, we elucidate the potential link between chronic hepatitis C-associated inflammation and alterati
24 % credible interval 30-44), the incidence of chronic hepatitis C by 37% (29-44), and chronic hepatiti
25 atments have reduced the prevalence of adult chronic hepatitis C by a median 37% (95% credible interv
27 Here, we demonstrate in 1689 patients with chronic hepatitis C (CHC) (1,501 with CHC and 188 with H
28 ] allele is more represented in HCC cases in chronic hepatitis C (CHC) and alcoholic liver disease (A
29 Most of these markers have been developed in chronic hepatitis C (CHC) and nonalcoholic fatty liver d
31 FLD and liver damage progression in NASH and chronic hepatitis C (CHC) by still undefined mechanisms,
33 mproving prediction of treatment outcomes in chronic hepatitis C (CHC) genotype 4 (G4) is necessary t
40 proving hepatic fibrosis and inflammation in chronic hepatitis C (CHC) patients after eradication wit
41 (TVR)-based TT in untreated genotype 1 (G1) chronic hepatitis C (CHC) patients discriminated accordi
43 se (ALT) elevation and associated factors in chronic hepatitis C (CHC) patients who achieved undetect
46 es in metabolic and inflammatory outcomes in chronic hepatitis C (CHC) patients: low-density lipoprot
48 pe of hepatitis C virus (HCV) treatment, but chronic hepatitis C (CHC) remains a leading indication f
49 about mortality rates (MRs) in patients with chronic hepatitis C (CHC) with cirrhosis is limited.
50 hort of 4,172 patients, including 3,129 with chronic hepatitis C (CHC), 555 with chronic hepatitis B
51 nic course: n = 17), 12 HIV(+) patients with chronic hepatitis C (CHC), 8 HIV monoinfected individual
52 ith confirmed early PBC, 10 with early stage chronic hepatitis C (CHC), and nine with resolving, self
54 epatitis C virus (HCV) is a leading cause of chronic hepatitis C (CHC), liver cirrhosis, and hepatoce
55 t hepatitis C virus (HCV) infection leads to chronic hepatitis C (CHC), which often progresses to liv
64 allenges include increasing awareness of the chronic hepatitis C epidemic, garnering sufficient publi
65 e inhibitors as part of standard therapy for chronic hepatitis C genotype 1 infection, drug-drug inte
70 terferon (PEG-IFN)-alpha in the treatment of chronic hepatitis C has led to an increase in sustained
74 pproved for response-guided-therapy (RGT) of chronic hepatitis C (HCV) genotype-1-infection in treatm
75 f Ledipasvir/Sofosbuvir for the treatment of chronic hepatitis C (HCV) includes the truncation of the
80 liver damage, especially in individuals with chronic hepatitis C (HCV); however, the impact of nonhea
82 the management of acute infectious diseases, chronic hepatitis C, human immunodeficiency virus, and a
84 ong the estimated 150 000 adults living with chronic hepatitis C in Georgia, 52 856 (35.1%) were diag
85 Among estimated 150,000 adults living with chronic hepatitis C in Georgia, 52,856 (35.1%) were diag
86 ession analysis, methadone doses (P = .005), chronic hepatitis C-induced cirrhosis (P = .008), and be
87 ors for prolongation of the QTc interval are chronic hepatitis C-induced cirrhosis, higher methadone
88 the past decade, the standard treatment for chronic hepatitis C infection has been pegylated-interfe
89 Compared with other countries, patients with chronic hepatitis C infection in Japan tend to be older,
91 of hepatitis and fibrosis progression during chronic hepatitis C infection, while contrasting results
96 nterferon-free regimens for the treatment of chronic hepatitis C infections needs to be evaluated in
99 erexpression of FBP1 in most HCC tumors with chronic hepatitis C is significantly linked with the dec
101 ymorphisms at ITPA and treatment efficacy in chronic hepatitis C mediated by reduced relapse risk.
102 e of chronic hepatitis C by 37% (29-44), and chronic hepatitis C mortality by 14% (3-30) and have pre
103 ame organ (liver) derived from patients with chronic hepatitis C: On the one side, cirrhotic and tumo
104 mbined cohort of non-cirrhotic patients with chronic hepatitis C or alcoholic liver disease (n = 1121
115 n-free, direct-acting antiviral treatment of chronic hepatitis C, subjects who received ribavirin had
116 t has recently been applied to patients with chronic hepatitis C, successfully clearing hepatitis C v
119 notype affects the response of patients with chronic hepatitis C to peginterferon and ribavirin, litt
126 y activity and fibrosis in 551 patients with chronic hepatitis C virus (HCV) and 203 patients with ch
129 ring nonalcoholic steatohepatitis (NASH) and chronic hepatitis C virus (HCV) compared to alcohol live
130 efficacy and safety in a phase IIa study in chronic hepatitis C virus (HCV) genotype (GT)-1-infected
131 for 24 weeks was recently approved to treat chronic hepatitis C virus (HCV) genotype 1 (GT-1) infect
132 proved in the United States for treatment of chronic hepatitis C virus (HCV) genotype 1 and 4 infecti
133 proved in the United States for treatment of chronic hepatitis C virus (HCV) genotype 1 and 4 infecti
134 hase 3 study in previous non-responders with chronic hepatitis C virus (HCV) genotype 1 infection and
136 telaprevir in treatment-naive patients with chronic hepatitis C virus (HCV) genotype 1 infection, in
137 virin in treatment-experienced patients with chronic hepatitis C virus (HCV) genotype 1 infection.
138 virin (RBV) in treatment-naive patients with chronic hepatitis C virus (HCV) genotype 1 without cirrh
139 ective in previously untreated patients with chronic hepatitis C virus (HCV) genotype 1, 2, or 3 infe
140 lated with pibrentasvir is approved to treat chronic hepatitis C virus (HCV) genotype 1-6 infection i
141 tions are rapidly evolving for patients with chronic hepatitis C virus (HCV) genotype 1b (GT1b) infec
143 eatment with peginterferon and ribavirin for chronic hepatitis C virus (HCV) genotype 2 or 3 infectio
144 ermine the optimal regimen for patients with chronic hepatitis C virus (HCV) genotype 2, 3, 4, or 6 i
145 ed regimens in treatment-naive patients with chronic hepatitis C virus (HCV) genotype 4 infection.
146 ear, the landscape of therapy for genotype 1 chronic hepatitis C virus (HCV) has changed dramatically
148 nomic burden imposed by the complications of chronic hepatitis C virus (HCV) infection - including ci
149 rect-acting antiviral agents that can cure a chronic hepatitis C virus (HCV) infection after 8-12 wee
151 ng evidence indicates an association between chronic hepatitis C virus (HCV) infection and B-cell lym
152 ns are needed for treatment of patients with chronic hepatitis C virus (HCV) infection and cirrhosis.
153 s is a frequent complication associated with chronic hepatitis C virus (HCV) infection and is a key p
154 previr regimen for 12 weeks in patients with chronic hepatitis C virus (HCV) infection and stage 4-5
155 ole of MAIT cells in livers of patients with chronic hepatitis C virus (HCV) infection and their fate
157 trials have demonstrated that patients with chronic hepatitis C virus (HCV) infection associated HCC
161 ons in the peripheral blood of patients with chronic hepatitis C virus (HCV) infection compared to su
162 An unbiased genome-to-genome analysis in chronic hepatitis C virus (HCV) infection confirms the i
164 d neurocognitive impairment in patients with chronic hepatitis C virus (HCV) infection even before li
165 eron-alpha (IFNalpha) has been used to treat chronic hepatitis C virus (HCV) infection for over 20 ye
170 direct-acting antiviral (DAA) therapies for chronic hepatitis C virus (HCV) infection have demonstra
173 nd: Use of interferon and ribavirin to treat chronic hepatitis C virus (HCV) infection in kidney tran
174 Use of interferon and ribavirin to treat chronic hepatitis C virus (HCV) infection in kidney tran
175 interferon- and ribavirin-free treatment for chronic hepatitis C virus (HCV) infection in patients co
177 to improve access to care and treatment for chronic hepatitis C virus (HCV) infection in resource-li
180 herapy can safely prevent the development of chronic hepatitis C virus (HCV) infection in uninfected
187 , interferon-alpha (IFN-alpha) treatment for chronic hepatitis C virus (HCV) infection is an ideal mo
190 A key question in care of patients with chronic hepatitis C virus (HCV) infection is beginning t
199 and ribavirin (IFN-alpha/RBV) treatment for chronic hepatitis C virus (HCV) infection is influenced
204 of liver disease in untreated children with chronic hepatitis C virus (HCV) infection is poorly docu
206 e status in liver and blood of patients with chronic hepatitis C virus (HCV) infection long after the
207 th human immunodeficiency virus (HIV) and/or chronic hepatitis C virus (HCV) infection may be prescri
211 ere are no effective and safe treatments for chronic hepatitis C virus (HCV) infection of patients wh
214 increases treatment efficacy for genotype 1 chronic hepatitis C virus (HCV) infection versus PEG-IFN
217 ee, complete regimen for adult patients with chronic hepatitis C virus (HCV) infection without cirrho
219 ting antivirals (DAAs) effectively eradicate chronic hepatitis C virus (HCV) infection, although HCV
221 have recently been approved for treatment of chronic hepatitis C virus (HCV) infection, are more effi
222 to a high cure rate in treated patients with chronic hepatitis C virus (HCV) infection, but this stil
223 d with clinical and histological features of chronic hepatitis C virus (HCV) infection, including nec
224 nterferon and ribavirin for the treatment of chronic hepatitis C virus (HCV) infection, increase the
225 For children under 12 years of age who have chronic hepatitis C virus (HCV) infection, there are cur
226 course of direct-acting antiviral agents for chronic hepatitis C virus (HCV) infection, we examined t
227 ect-acting antivirals (DAA) for treatment of chronic hepatitis C virus (HCV) infection, we looked at
228 ent standard of care combination therapy for chronic hepatitis C virus (HCV) infection, yet the compo
254 nterferon-free regimens for the treatment of chronic hepatitis C virus (HCV) infections require furth
255 The evolution of treatment for patients with chronic hepatitis C virus (HCV) is evolving at a rapid p
256 e direct-acting antivirals (DAA) in treating chronic hepatitis C virus (HCV) is limited by low screen
257 The global burden of disease attributable to chronic hepatitis C virus (HCV) is very large, yet the u
258 1 healthy individuals (NC) (n = 20), group 2 chronic hepatitis C virus (HCV) patients (n = 20), group
261 ntibodies (FPAs) have been well described in chronic hepatitis C virus (HCV), this has not been evalu
263 the risk of chronic kidney disease (CKD) in chronic hepatitis C virus (HCV)-infected patients and th
272 evir + TMC647055/ritonavir + JNJ-56914845 in chronic hepatitis C virus genotype (GT)1-infected treatm
274 afe and highly effective in adolescents with chronic hepatitis C virus genotype 2 or 3 infection.
275 ns with or without ribavirin as treatment of chronic hepatitis C virus in solid organ transplant reci
279 -acting antiviral drugs for the treatment of chronic hepatitis C virus infection have reduced mortali
280 pulations after DAA therapy in patients with chronic hepatitis C virus infection in the context of th
283 ffective and well tolerated in patients with chronic hepatitis C virus infection, including those wit
284 nse (SVR) to interferon-based treatments for chronic hepatitis C virus infection, whereas Asian race
289 iling the response to interferon therapy (in chronic Hepatitis C virus patients) and Influenza A viru
290 le degree of liver fibrosis in patients with chronic hepatitis C virus prohibiting cadaveric renal tr
291 acting antiviral agents for the treatment of chronic hepatitis C virus that have significantly increa
293 atocellular carcinoma (HCC) in patients with chronic hepatitis C virus; however, their impact in pati
294 lular carcinoma was overrepresented, whereas chronic hepatitis C was underrepresented, in reported Un
295 ting new direct-acting antivirals (DAAs) for chronic hepatitis C were the major focus of interest at
296 This represents a major difference from chronic hepatitis C, where numerous previous studies hav
297 wo cases of HBV reactivation and one case of chronic hepatitis C, which were successfully treated.
299 To address this issue, 126 patients with chronic hepatitis C who completed pegylated IFN plus rib