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1 role for IFI16 in protection against genital herpes.
2 transmission, through prevention of neonatal herpes.
3 ompared with control patients without ocular herpes.
4 ted with protection against recurrent ocular herpes.
5 ichomoniasis (1 study; n = 779), and genital herpes (1 study; n = 779).
6         In a cohort of patients with genital herpes and healthy controls, the minor G allele of the I
7 rus 1 (HSV-1) causes cold sores and neonatal herpes and is a leading cause of blindness.
8 l estimates of the annual number of neonatal herpes cases during 2010-15.
9          We estimated that the most neonatal herpes cases occurred in Africa, due to high maternal HS
10 ula, gastroenteritis, viral gastroenteritis, herpes dermatitis, multiple fractures, respiratory failu
11 considered antiretrovirals, such as the anti-herpes drugs Aciclovir and Ganciclovir and the anti-canc
12 cted with HSV-1 KOS, which induces transient herpes epithelial keratitis without herpes stromal kerat
13               INTERPRETATION: These neonatal herpes estimates mark the first attempt to quantify the
14          Herpes simplex virus type 2 (HSV-2; herpes) exacerbates human immunodeficiency virus type 1
15            Some infections by viruses in the herpes family are more common in the earlier childbearin
16 transgenic mice and reduced recurrent ocular herpes following UV-B-induced reactivation.
17 tance in CD8(+) T cell immunity to recurrent herpes has been poorly elucidated.
18 eutic strategies to treat blinding recurrent herpes infection and disease.
19               Using a mouse model of genital herpes infection, we demonstrate that both antibodies an
20                                     Neonatal herpes infection, while uncommon, can result in substant
21 upper respiratory tract infections, and oral herpes infections were more frequent with ocrelizumab th
22 against primary and secondary female genital herpes infections.
23 n global estimates of the number of neonatal herpes infections.
24                          Importance: Genital herpes is a prevalent sexually transmitted infection in
25                                     Neonatal herpes is a rare but potentially devastating condition w
26    Caused by the herpes simplex virus (HSV), herpes is a viral infection that is one of the most wide
27 d Relevance: Serologic screening for genital herpes is associated with a high rate of false-positive
28                                              Herpes is associated with phenotypic changes in CD4+ T-c
29 tter collection of primary data for neonatal herpes is crucially needed to reduce uncertainty and ref
30 es extract for the prophylactic treatment of herpes labialis and suggest possible activity of Ca-SP a
31                      Many viruses, including herpes simplex (HSV), are recruited to their host cells
32                                              Herpes simplex encephalitis (HSE) is the most common for
33 cent reviews; these include the relevance of herpes simplex encephalitis and of epilepsy to AD, the a
34 netic association between TRIF mutations and herpes simplex encephalitis in patients.
35 l intervention is crucial to the survival of herpes simplex encephalitis patients; however, many surv
36  including necrotizing stromal keratitis and herpes simplex encephalitis.
37 ), polyoma (BK) viremia (8.2% vs 11.1%), and herpes simplex infections (5.5% vs 4.0%).
38 ree patients with a unilateral and relapsing herpes simplex keratitis (HSK group) that was quiescent
39 ity of life (QoL) in patients with quiescent herpes simplex keratitis compared with control patients
40 al patients were diagnosed sequentially with herpes simplex keratitis, then Acanthamoeba keratitis be
41  for dendritiform keratopathy, such as prior herpes simplex keratitis, varicella-zoster viral keratit
42 ated with antiviral medications for presumed herpes simplex keratitis; 4 patients underwent diagnosti
43 petic anterior uveitis (AU), owing to either herpes simplex or varicella zoster virus, by using the S
44 lopment of a safe and effective asymptomatic herpes simplex vaccine that is selectively based on CD8(
45 lopment of a safe and effective T-cell-based herpes simplex vaccine.
46 this assessment include adenovirus 8 and 19, herpes simplex virus (HSV) 1 and 2, human immunodeficien
47                                              Herpes simplex virus (HSV) 1 stimulates type I IFN expre
48 dy of neurotropic viruses in vitroIMPORTANCE Herpes simplex virus (HSV) affects millions of people wo
49 tions that US9 is neuron specific.IMPORTANCE Herpes simplex virus (HSV) and other alphaherpesviruses,
50                                              Herpes simplex virus (HSV) anterograde transport in neur
51  a broad antimicrobial factor that restricts herpes simplex virus (HSV) by activating type I interfer
52                                          The herpes simplex virus (HSV) capsid is released into the c
53 his study employed a novel strategy in which herpes simplex virus (HSV) carrying a small interfering
54                                              Herpes simplex virus (HSV) causes acute and relapsing sy
55 fluid (CSF) commonly predicts the absence of herpes simplex virus (HSV) central nervous system (CNS)
56                      During lytic infection, herpes simplex virus (HSV) DNA is replicated by a mechan
57                                              Herpes simplex virus (HSV) entry into a subset of cells
58 erpesvirus entry mediator (HVEM) facilitates herpes simplex virus (HSV) entry through interactions wi
59                                              Herpes simplex virus (HSV) establishes a latent reservoi
60                                              Herpes simplex virus (HSV) establishes latency and react
61 is known as a transcriptional coactivator of herpes simplex virus (HSV) immediate early (IE) transcri
62                                          The herpes simplex virus (HSV) infected cell culture polypep
63  Neuron-virus interactions that occur during herpes simplex virus (HSV) infection are not fully under
64                                              Herpes simplex virus (HSV) infection is restricted to ep
65                                              Herpes simplex virus (HSV) infection is widespread in th
66                                              Herpes simplex virus (HSV) infections of the central ner
67                             The terminase of herpes simplex virus (HSV) is composed of three subunits
68 pediatric penetrating keratoplasty (PPK) for herpes simplex virus (HSV) keratitis.
69 ctivator HCF-1 is required for initiation of herpes simplex virus (HSV) lytic infection and for react
70 f aqueous or vitreous humor was positive for herpes simplex virus (HSV) or varicella zoster virus (VZ
71 od to visualize pseudorabies virus (PRV) and herpes simplex virus (HSV) particles in living cells.
72                             Despite frequent herpes simplex virus (HSV) reactivation, peripheral nerv
73                             The rate of oral herpes simplex virus (HSV) shedding was lower overall, a
74                      Chronic infections with herpes simplex virus (HSV) type 1 are highly prevalent i
75                                          The herpes simplex virus (HSV) type I alkaline nuclease, UL1
76 e by microinjecting before training a single herpes simplex virus (HSV) vector expressing either CRIS
77                    Presence of CMV, EBV, and herpes simplex virus (HSV) were independent predictors o
78                                Caused by the herpes simplex virus (HSV), herpes is a viral infection
79     Infection is caused by 2 subtypes of the herpes simplex virus (HSV), HSV-1 and HSV-2.
80 itro nanomolar irreversible activity against herpes simplex virus (HSV), human papilloma virus, respi
81  cell entry and subsequent lateral spread of herpes simplex virus (HSV), requires the four envelope g
82                                              Herpes simplex virus (HSV), which triggers the STING sig
83 cally significant species of simplexviruses, herpes simplex virus (HSV)-1 and HSV-2, with estimated d
84                                           In herpes simplex virus (HSV)-infected cells, ND10 bodies a
85 creased) particle-to-PFU ratio in vitro than herpes simplex virus (HSV).
86 enchymal brain inflammation, commonly due to herpes simplex virus (HSV).
87 interferon (IFN) is important for control of herpes simplex virus (HSV-1) in the central nervous syst
88  alone mediates recognition and clearance of herpes simplex virus (HSV1)-infected cells.
89  ablation on tga20/CD11b-thymidine kinase of Herpes simplex virus (HSVTK) cerebellar organotypic cult
90                                    Oncolytic herpes simplex virus (oHSV) selectively replicates in ca
91 nd tested the fate and efficacy of oncolytic herpes simplex virus (oHSV)-armed mesenchymal stem cells
92 n of foreign DNA-sensing pathways.IMPORTANCE Herpes simplex virus 1 (HSV-1) afflicts 80% of the popul
93                                              Herpes simplex virus 1 (HSV-1) and HSV-2 are large, doub
94 f UL37 homologs from two alphaherpesviruses, herpes simplex virus 1 (HSV-1) and pseudorabies virus (P
95 ar disease in virus-infected mice.IMPORTANCE Herpes simplex virus 1 (HSV-1) causes cold sores and neo
96                                              Herpes simplex virus 1 (HSV-1) encodes the multifunction
97 ponent of cell membranes and is required for herpes simplex virus 1 (HSV-1) entry (1-3).
98                        The dissection of the herpes simplex virus 1 (HSV-1) entry mechanism is compli
99 ined whether Cbl mediates the removal of the herpes simplex virus 1 (HSV-1) entry receptor Nectin-1 f
100                                              Herpes simplex virus 1 (HSV-1) establishes latency withi
101                                              Herpes simplex virus 1 (HSV-1) establishes lifelong infe
102 ultaneous presence of a helper virus such as herpes simplex virus 1 (HSV-1) for productive replicatio
103 plication greatly enhances expression of the herpes simplex virus 1 (HSV-1) gamma2 late genes by stil
104 gp120) construct fused to a small portion of herpes simplex virus 1 (HSV-1) glycoprotein D (gD) so th
105                                          The herpes simplex virus 1 (HSV-1) ICP0 protein is an E3 ubi
106 mia nuclear bodies (PML NBs), is a target of herpes simplex virus 1 (HSV-1) ICP0-mediated degradation
107                                              Herpes simplex virus 1 (HSV-1) infection is an incurable
108                                              Herpes simplex virus 1 (HSV-1) infection is widespread a
109 efects in IFN responses can result in lethal herpes simplex virus 1 (HSV-1) infections, usually from
110                                              Herpes simplex virus 1 (HSV-1) infects most people and c
111          The immediate early protein ICP0 of herpes simplex virus 1 (HSV-1) interacts with CIN85, an
112                  We report here that UL37 of herpes simplex virus 1 (HSV-1) is a protein deamidase th
113                                        Human herpes simplex virus 1 (HSV-1) is a widespread pathogen,
114                 The UL16 tegument protein of herpes simplex virus 1 (HSV-1) is conserved among all he
115                                              Herpes simplex virus 1 (HSV-1) is one of the eight herpe
116  viral DNA from NPC-bound capsids.IMPORTANCE Herpes simplex virus 1 (HSV-1) is the causative agent of
117 nal (NLS) sequences previously identified in herpes simplex virus 1 (HSV-1) large terminase and human
118                                              Herpes simplex virus 1 (HSV-1) latency entails the repre
119 s from a variant to target the mRNA encoding herpes simplex virus 1 (HSV-1) major transcription regul
120                                              Herpes simplex virus 1 (HSV-1) most commonly causes recr
121 ve previously shown that the live-attenuated herpes simplex virus 1 (HSV-1) mutant lacking the nuclea
122                                              Herpes simplex virus 1 (HSV-1) remodels nuclear membrane
123 was to reexamine the requirement of UL21 for herpes simplex virus 1 (HSV-1) replication.
124        Infection of mature HD10.6 neurons by herpes simplex virus 1 (HSV-1) results in a delayed but
125                        Ocular infection with herpes simplex virus 1 (HSV-1) sets off an inflammatory
126 sRNA, encephalomyocarditis virus (EMCV), and herpes simplex virus 1 (HSV-1) show impaired production
127 nd ICP34.5 are among the proteins encoded by herpes simplex virus 1 (HSV-1) that modulate type I IFN
128 e ability of the prototypic alphaherpesvirus herpes simplex virus 1 (HSV-1) to enter neurons via axon
129                                              Herpes simplex virus 1 (HSV-1) UL20 plays a crucial role
130                                          The herpes simplex virus 1 (HSV-1) UL37 protein functions in
131   Herein, we report that the live-attenuated herpes simplex virus 1 (HSV-1) VC2 vaccine strain, which
132   Following infection of epithelial tissues, herpes simplex virus 1 (HSV-1) virions travel via axonal
133 lected TRIM proteins in autophagy induced by herpes simplex virus 1 (HSV-1), encephalomyocarditis vir
134                Persistent pathogens, such as herpes simplex virus 1 (HSV-1), have evolved a variety o
135 roinvasive alphaherpesviruses, such as human herpes simplex virus 1 (HSV-1), HSV-2, and veterinarian
136 trast, of the more than 80 mRNAs harbored by herpes simplex virus 1 (HSV-1), only 5 are spliced.
137                     Following infection with herpes simplex virus 1 (HSV-1), PIAS1 is recruited to nu
138  Here we focus on two tegument proteins from herpes simplex virus 1 (HSV-1), pUL7 and pUL51, which ha
139       Although many herpesviruses, including herpes simplex virus 1 (HSV-1), stimulate mTORC1, how HS
140 zuelan equine encephalitis virus (VEEV), and herpes simplex virus 1 (HSV-1), suggesting that LIMK inh
141                                          For herpes simplex virus 1 (HSV-1), we and others have previ
142                                              Herpes simplex virus 1 (HSV-1), which causes a variety o
143                                Although most herpes simplex virus 1 (HSV-1)-infected individuals shed
144 esponse to restrict viral pathogens, such as herpes simplex virus 1 (HSV-1).
145 SP141), bound to RIG-I during infection with herpes simplex virus 1 (HSV-1).
146  between AAV2 and one of its helper viruses, herpes simplex virus 1 (HSV-1).
147 f mice that have been ocularly infected with herpes simplex virus 1 (HSV-1).
148  choriomeningitis virus (LCMV) infection, or herpes simplex virus 1 (HSV1) infection was profoundly d
149 us agalactiae, cytomegalovirus, enterovirus, herpes simplex virus 1 and 2, human herpesvirus 6, human
150  ability to be infected by the herpesviruses herpes simplex virus 1 and murine herpesvirus 68 and the
151  Here, we have characterized the full-length herpes simplex virus 1 gB in a native membrane by displa
152 pted this method to rapidly deliver a 152 kb herpes simplex virus 1 genome cloned in yeast into mamma
153 e the molecular organization of chromatin in herpes simplex virus 1 infection and its effect on the t
154 promised survival during influenza virus and herpes simplex virus 1 infections.
155 er replication of BKV, whereas influenza and herpes simplex virus 1 replication were clearly reduced.
156  study focuses on two tegument proteins from herpes simplex virus 1 that are conserved in all herpesv
157 tein domains, as well as a truncated form of herpes simplex virus 1 thymidine kinase (HSV-TK).
158 wed evidence of acute herpesvirus infection; herpes simplex virus 1 was found most often.
159 tudy, the structural, material properties of herpes simplex virus 1 were investigated.
160 e, whereas infection with influenza A virus, herpes simplex virus 1, or cytomegalovirus induced a str
161                     Random walk modelling of herpes simplex virus 1-sized particles in a three-dimens
162 viously established that cells infected with herpes simplex virus 2 (HSV-2) are disrupted in their ab
163      Several prophylactic vaccines targeting herpes simplex virus 2 (HSV-2) have failed in the clinic
164 llions of people worldwide are infected with herpes simplex virus 2 (HSV-2), and to date, an efficaci
165                 Alpha herpesviruses, such as herpes simplex virus and pseudorabies virus (PRV), are n
166 5 on the structural stability of icosahedral herpes simplex virus capsids.
167 ital specimens each containing >/=105 copies herpes simplex virus DNA/ml collected a median of 5 mont
168           The transcription factor ICP4 from herpes simplex virus has a central role in regulating th
169 h inhibits HIV-1, HIV-2, Influenza virus and herpes simplex virus infection, and enhances the potenti
170 icase-primase inhibitor for the treatment of herpes simplex virus infections, was prepared.
171 r development of antiviral agents.IMPORTANCE Herpes simplex virus is a major pathogen, and although n
172                                The capsid of herpes simplex virus is built up of a variety of protein
173 ovir decreased the recurrence of any type of herpes simplex virus keratitis by approximately half.
174 nfections of the superficial cornea, such as herpes simplex virus keratitis or Acanthamoeba keratitis
175 ) relocation of nonintegrin receptors (e.g., herpes simplex virus nectin1 and Kaposi's sarcoma-associ
176 h clinically diagnosed ARN, PCR-positive for herpes simplex virus or varicella zoster virus and evalu
177 iral reactivation, exhibiting parallels with herpes simplex virus reactivation.
178  of the lipid raft-dwelling US9 protein from Herpes Simplex Virus strikingly overlaps with that of th
179 transgenic mice expressing the suicide gene, herpes simplex virus thymidine kinase (HSVtk), driven by
180 g AAVP particles served to deliver the human Herpes simplex virus thymidine kinase type-1 (HSVtk) gen
181                 Infectious titers of EBOV or herpes simplex virus type 1 (HSV-1) in detergents-treate
182                         Lytic infection with herpes simplex virus type 1 (HSV-1) induces profound mod
183                                              Herpes simplex virus type 1 (HSV-1) is a leading cause o
184                       Glycoprotein D (gD) of herpes simplex virus type 1 (HSV-1) is one of four glyco
185 lly occurs during delivery from mothers with herpes simplex virus type 1 (HSV-1) or type 2 (HSV-2) ge
186 ological stress.IMPORTANCE Like all viruses, herpes simplex virus type 1 (HSV-1) reproduction relies
187 we reported a new series of highly defective herpes simplex virus type 1 (HSV-1) vectors that were fu
188 ormational approach to genome engineering of herpes simplex virus type 1 (HSV-1), which has a large D
189                   Knockout of TRIM14 impairs herpes simplex virus type 1 (HSV-1)-triggered antiviral
190                 Support for the concept that herpes simplex virus type 1 (HSV1), when present in the
191                                              Herpes simplex virus type 1 and Alzheimer's disease: pos
192 athway are associated with susceptibility to herpes simplex virus type 1 encephalitis (HSE).
193   We found wide distribution of O-glycans on herpes simplex virus type 1 glycoproteins and demonstrat
194  gene encoding the prodrug-converting enzyme herpes simplex virus type 1 thymidine kinase (HSV1-tk) i
195                                         CMV, herpes simplex virus type 1, and human herpesvirus 6 inf
196 e association of 4 human herpesviruses (CMV, herpes simplex virus type 1, human herpesvirus type 6, a
197  pathogens were detected by mNGS (4 cases of herpes simplex virus type 1, including 1 case of coinfec
198 fumarate (TDF) has in vitro activity against herpes simplex virus type 2 (HSV-2) and reduced HSV-2 ac
199               Despite the high prevalence of herpes simplex virus type 2 (HSV-2) in sub-Saharan Afric
200                                      Genital herpes simplex virus type 2 (HSV-2) infection causes rec
201 mmune system's protective effect against one herpes simplex virus type 2 (HSV-2) infection protects a
202 or NK cell function in response to a mucosal herpes simplex virus type 2 (HSV-2) infection.
203                                      HIV and herpes simplex virus type 2 (HSV-2) infections cause a s
204 ART) has been incompletely characterized for herpes simplex virus type 2 (HSV-2).
205                                              Herpes simplex virus type 2 (HSV-2; herpes) exacerbates
206 against cervical cancer, cervical dysplasia, herpes simplex virus type 2, chlamydia, and syphilis.
207 f herpetic neuralgia using a murine model of Herpes Simplex Virus Type-1 (HSV-1) infection.
208 CB) women, including bacterial vaginosis and herpes simplex virus type-2 (HSV-2) infection.
209 he impact of antiretroviral therapy (ART) on herpes simplex virus type-2 (HSV-2) replication is uncle
210 ded controls for sociodemographic variables, herpes simplex virus type-2 status, and recreational dru
211 rr virus (EBV), human herpesvirus 6 (HHV-6), herpes simplex virus types 1 (HSV-1) and 2 (HSV-2), and
212 ein Barr virus (EBV), cytomegalovirus (CMV), herpes simplex virus types 1 and 2, human herpesvirus 8)
213 iency virus, hepatitis B virus, and neonatal herpes simplex virus, from which lessons for the evaluat
214 ing of mucosal immunity and then compare the herpes simplex virus, human immunodeficiency virus, and
215  papilloma virus, hepatitis B and C viruses, herpes simplex virus, norovirus, rotavirus, parvovirus,
216 use substantial impairment: cytomegalovirus, herpes simplex virus, rubella virus, Toxoplasma gondii,
217 ded toxoplasmosis, rubella, cytomegalovirus, herpes simplex virus, syphilis, and human immunodeficien
218 97%; PPV range, 52%-95%; NPV range, 79%-80%; herpes simplex virus, vulvar ulcerations: sensitivity, 2
219                                              Herpes simplex virus-1 (HSV-1) causes life-long morbidit
220                                              Herpes Simplex Virus-1 (HSV-1) is a ubiquitous human pat
221 76-9 (MHC I low) tumors respond to oncolytic herpes simplex virus-1 (oHSV-1) and PD-1 blockade combin
222 ers in the lung, and are resistant to lethal herpes simplex virus-1 infection due to enhanced product
223 Here, we address this deficit, focusing on a herpes simplex virus-1 protein, ICP27.
224                    Furthermore, an unrelated herpes simplex virus-thymidine kinase (HSV-TK) promoter
225 r, and parvovirus B19), cytomegalovirus, and herpes simplex virus.
226 e fusion also proved to be well tolerated in herpes simplex virus.
227                                              Herpes simplex viruses (HSV) are human pathogens that sw
228  significant effect.IMPORTANCE Infections by herpes simplex viruses (HSV) cause painful cold sores or
229                                              Herpes simplex viruses 1 and 2 (HSV-1 and HSV-2) infect
230 rus, mumps virus, measles virus, lyssavirus, herpes simplex viruses 1 and 2, Epstein-Barr virus, ente
231 domains from the Drosophila fushi tarazu and Herpes simplex VP16 was created.
232 polymerase chain reaction (PCR) analysis for Herpes simplex, varicella zoster, cytomegalovirus, Epste
233 ere independent of varicella-zoster virus or herpes-simplex virus 1 coinfection.
234 viruses: KSHV, Epstein-Barr virus (EBV), and herpes simplexvirus-2 (HSV-2).
235 ransient herpes epithelial keratitis without herpes stromal keratitis sequelae, possessed a significa
236 transient discomfort to the blinding disease herpes stromal keratitis, yet most patients experience a
237 ngs, a novel "prime/pull" therapeutic ocular herpes vaccine strategy is proposed and discussed.
238                      This study shows that a herpes viral infection of FMs sensitizes the tissue to l
239 a-associated lymphoid tissue lymphoma, human herpes virus (HHV)-6, HHV-7, chlamydia, Epstein-Barr vir
240                  Kaposi's sarcoma-associated herpes virus (KSHV) polyadenylated nuclear (PAN) RNA fac
241                                        Human herpes virus 8 (HHV-8), also known as Kaposi's sarcoma a
242 tivity; 14.9% (95% CI: 12.4-17.4%) for human herpes virus 8 infection.
243  Kaposi sarcoma-associated herpesvirus/human herpes virus 8 replication and uptake of the ORF45 tegum
244  Kaposi sarcoma-associated herpesvirus/human herpes virus 8.
245 ng respiratory virus infection, we show that herpes virus entry mediator (HVEM; TNFRSF14), a member o
246          Epstein-Barr virus (EBV) is a human herpes virus that infects >90% of individuals.
247  cancer), viral (e.g., human papillomavirus, herpes virus) and bacterial (e.g., Helicobacter pylori,
248 ovirus (HCMV) is the prototypical human beta-herpes virus.
249                                We found that herpes viruses (e.g., subtypes HHV4, HHV5, and HHV6) tha
250 ivo human tonsillar tissue system) and human herpes viruses.
251 of activity that also covers hepatitis B and herpes viruses.
252              Serologic screening for genital herpes was associated with psychosocial harms, including
253        Globally the overall rate of neonatal herpes was estimated to be about ten cases per 100 000 l
254 erial vaginosis, trichomoniasis, and genital herpes was performed in a high-prevalence population wit
255                         Persons with genital herpes were randomized into 3 dose cohorts to receive 3
256  1.04; 95% confidence interval 1.00-1.08) or herpes zoster (adjusted HR 1.03; 95% confidence interval
257   Tens of millions of seniors are at risk of herpes zoster (HZ) and its complications.
258 on emergency department (ED) utilization for herpes zoster (HZ) has not been examined to date.
259       Temporal increases in the incidence of herpes zoster (HZ) have been reported but studies have e
260                The incidence and severity of herpes zoster (HZ) increases with age.
261                           Protection against herpes zoster (HZ) induced by the live attenuated zoster
262 e in a healthy population, the protection of herpes zoster (HZ) vaccine in end-stage renal disease (E
263 on for the four catch-up cohorts was 33% for herpes zoster (incidence rate ratio 0.67 [0.61-0.74]) an
264                                              Herpes zoster (shingles) causes significant morbidity in
265 equivalent to about 17 000 fewer episodes of herpes zoster and 3300 fewer episodes of postherpetic ne
266 a vaccine effectiveness of about 62% against herpes zoster and 70-88% against postherpetic neuralgia.
267 o estimate vaccine coverage and incidence of herpes zoster and postherpetic neuralgia consultations.
268 of the vaccination programme on incidence of herpes zoster and postherpetic neuralgia in this populat
269 ultations with patients aged 60-89 years for herpes zoster and postherpetic neuralgia occurring betwe
270 cinations administered and consultations for herpes zoster and postherpetic neuralgia, and aggregated
271 ce-attenuated vaccine against chickenpox and herpes zoster and providing a new target for interventio
272                           To examine whether herpes zoster antigen (also called varicella-zoster viru
273                                              Herpes zoster antigen was detected in 3 of 25 temporal a
274 ups of patients, false-positive staining for herpes zoster antigen was detected in the presence of ca
275                  False-positive staining for herpes zoster antigen was detected on several temporal a
276                Among the GCA-negative group, herpes zoster antigen was not detected in any biopsy.
277  group, 3 patients had positive staining for herpes zoster antigen.
278 r virus is an important human pathogen, with herpes zoster being a major health issue in the aging an
279  is commonly thought to increase the risk of herpes zoster by causing immunosuppression.
280 c neuralgia is the most important symptom of herpes zoster disease and it is very difficult to treat.
281 c neuralgia is the most important symptom of herpes zoster disease, which is caused by Varicella zost
282  for the three routine cohorts, incidence of herpes zoster fell by 35% (incidence rate ratio 0.65 [95
283 ated varicella-zoster virus vaccine prevents herpes zoster in adults older than 50 years.
284  three serious infections, and four cases of herpes zoster in patients who received tofacitinib durin
285 oups, and the rates of overall infection and herpes zoster infection were higher with tofacitinib tha
286 s, there were four serious infections, three herpes zoster infections, one myocardial infarction, and
287  5175 person-years of follow-up, 26 cases of herpes zoster occurred among those assigned acyclovir, c
288 ical record can reliably be used to identify herpes zoster ophthalmicus cases.
289 s was noteworthy because the patient had had herpes zoster ophthalmicus diagnosed 3 weeks before the
290 e immunogenicity and safety of an adjuvanted herpes zoster subunit (HZ/su) vaccine when coadministere
291                          INTERPRETATION: The herpes zoster vaccination programme in England has had a
292                                   In 2013, a herpes zoster vaccination programme was introduced in En
293             We identified individual data on herpes zoster vaccinations administered and consultation
294                              Live attenuated herpes zoster vaccine (HZV) reduces that risk, although
295 l outcomes of myocardial infarction (MI) and herpes zoster were also studied.
296 ced transient local skin reactions: 1 (4.8%) herpes zoster, 3 (14.3%) transaminase elevation, and 1 (
297 eased incidences of cytomegalovirus disease, herpes zoster, BK virus, and nephropathy, which led to t
298 on for development of treatments for painful herpes zoster.
299 s a highly contagious agent of varicella and herpes zoster.
300 VZV) is the causative agent of varicella and herpes zoster.

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