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1 schedule of ages 6 and 10 weeks, along with oral poliovirus vaccine.
2 tbreaks were controlled within 6 months with oral poliovirus vaccine.
3 , 10.9 to 13.2), when her child received the oral poliovirus vaccine.
4 tion (WHO) recommends the discontinuation of oral poliovirus vaccine after eradication of wild poliov
5 type 1 oral poliovirus vaccine and trivalent oral poliovirus vaccine against type 1 paralytic poliomy
6 the estimated efficacy per dose of trivalent oral poliovirus vaccine against type 3 paralytic poliomy
8 ired the withdrawal of Sabin type 2 from the oral poliovirus vaccine and introduction of one or more
9 ed the field efficacies of monovalent type 1 oral poliovirus vaccine and trivalent oral poliovirus va
10 ted efficacies per dose of monovalent type 1 oral poliovirus vaccine and trivalent oral poliovirus va
11 he introduction of newly licensed monovalent oral poliovirus vaccines and new techniques of vaccine d
12 accine (four times as effective as trivalent oral poliovirus vaccine) and the moderate gains in cover
13 those who received azithromycin or placebo, oral poliovirus vaccine, and provided a blood sample acc
14 his is critical for the phased withdrawal of oral poliovirus vaccine, beginning with the type 2 compo
15 s vaccine (tOPV) with bivalent types 1 and 3 oral poliovirus vaccine (bOPV) and global introduction o
16 3 and the impact of bivalent (types 1 and 3) oral poliovirus vaccine (bOPV) use in immunization campa
22 text of making decisions about the timing of oral poliovirus vaccine cessation following global eradi
23 omycin did not improve the immunogenicity of oral poliovirus vaccine despite reducing biomarkers of e
24 years earlier) the patient received his last oral poliovirus vaccine dose, approximately 2 years befo
25 d an established poliovirus transmission and oral poliovirus vaccine evolution model to characterize
27 The higher efficacy of monovalent type 1 oral poliovirus vaccine (four times as effective as triv
28 the immunogenicity of serotype-3 monovalent oral poliovirus vaccine given to healthy infants living
30 ycin or placebo during a randomised trial of oral poliovirus vaccine immunogenicity (CTRI/2014/05/004
31 is finding is probably affected by the lower oral poliovirus vaccine immunogenicity previously demons
33 ssess the immunogenicity of the new bivalent oral poliovirus vaccine + inactivated poliovirus vaccine
34 18-week-old infants vaccinated with bivalent oral poliovirus vaccine/inactivated poliovirus vaccine r
36 itions where the efficacy of live-attenuated oral poliovirus vaccines is compromised by a high preval
38 vision of several doses of monovalent type 1 oral poliovirus vaccine (mOPV1) and bivalent OPV1 and 3
39 ssed the immunogenicity of monovalent type-1 oral poliovirus vaccine (mOPV1) given at shorter than us
40 ion activities (SIAs) with monovalent type 2 oral poliovirus vaccine (mOPV2) and novel type 2 oral po
43 nogenic polio vaccines, including monovalent oral poliovirus vaccines (mOPVs), are needed for supplem
44 poliovirus vaccine (mOPV2) and novel type 2 oral poliovirus vaccine (nOPV2) targeted an estimated 35
47 e number of newborns given the first dose of oral poliovirus vaccine (OPV) according to the RI schedu
48 lio Eradication Initiative plans to stop all oral poliovirus vaccine (OPV) after wild poliovirus erad
49 cting immunogenicity of the first 2 doses of oral poliovirus vaccine (OPV) among unimmunized Mayan in
51 ity profile after routine doses of trivalent oral poliovirus vaccine (OPV) and numerous supplemental
52 ed to improve the genetic stability of Sabin oral poliovirus vaccine (OPV) and reduce the emergence o
53 era, epitope-specific monoclonal murine anti-oral poliovirus vaccine (OPV) antibodies, and sera from
54 and the live attenuated Sabin strains in the oral poliovirus vaccine (OPV) are being removed sequenti
55 ins of poliovirus used in the manufacture of oral poliovirus vaccine (OPV) are prone to genetic varia
56 ths after vaccination with monovalent type 1 oral poliovirus vaccine (OPV) at 6 months and trivalent
58 ng model expectations with the experience of oral poliovirus vaccine (OPV) containing serotype 2 (OPV
59 e children whose caregivers refuse to accept oral poliovirus vaccine (OPV) contributes to the spread
61 on on immunisation activities with different oral poliovirus vaccine (OPV) formulations, and serotype
66 will entail eventual cessation of the use of oral poliovirus vaccine (OPV) in all countries to preven
67 is challenged by notions against the role of oral poliovirus vaccine (OPV) in eradicating contemporar
68 ared the immune response to IPV with that to oral poliovirus vaccine (OPV) in Guatemalan infants.
70 parents/caregivers if the child received any oral poliovirus vaccine (OPV) in Myanmar and, for younge
73 ut the degree of mucosal immunity induced by oral poliovirus vaccine (OPV) in tropical countries.
74 that all 124 countries currently using only oral poliovirus vaccine (OPV) introduce at least 1 dose
82 o before, throughout, and after the May 2010 oral poliovirus vaccine (OPV) mass immunization campaign
83 mune deficiency disorders (PIDD) who receive oral poliovirus vaccine (OPV) may transmit immunodeficie
84 tion is achieved, the use of live-attenuated oral poliovirus vaccine (OPV) must be discontinued becau
85 oliovirus vaccine in all 126 countries using oral poliovirus vaccine (OPV) only as of 2012, (2) full
88 the current national 4-dose live attenuated oral poliovirus vaccine (OPV) schedule with a 4-dose IPV
89 otide sequence identity) to the Sabin type 2 oral poliovirus vaccine (OPV) strain and unrelated (<82%
90 VDPV isolates differed from the Sabin type 1 oral poliovirus vaccine (OPV) strain at 1.84% to 3.15% o
91 efore and after a September 2007 switch from oral poliovirus vaccine (OPV) to IPV, using standard cov
92 hip existed between the failure of trivalent oral poliovirus vaccine (OPV) to prevent poliomyelitis a
94 int mutation at nucleotide (nt) 472 of Sabin oral poliovirus vaccine (OPV) type 3 is found in conjunc
95 shedding lend to the growing consensus that oral poliovirus vaccine (OPV) use should be discontinued
96 curred in 1979; however, as a consequence of oral poliovirus vaccine (OPV) use that began in 1961, an
97 d in human diploid cells and live attenuated oral poliovirus vaccine (OPV) was evaluated by randomiza
99 ion, and carrying-out mopping-up activities, oral poliovirus vaccine (OPV) was selected as the vaccin
100 cure a polio-free world, the live attenuated oral poliovirus vaccine (OPV) will eventually need to be
101 other orally administered vaccines, such as oral poliovirus vaccine (OPV), may also be associated wi
102 22 different interventions were assessed for oral poliovirus vaccine (OPV), oral rotavirus vaccine (R
104 ity of routine versus mass campaign doses of oral poliovirus vaccine (OPV), serum neutralizing antibo
122 he withdrawal of the serotype 2 component of oral poliovirus vaccine (OPV2) was implemented in April
124 poliovirus requires the global withdrawal of oral poliovirus vaccines (OPVs) and replacement with ina
125 ine-derived polioviruses (cVDPV2) from Sabin oral poliovirus vaccines (OPVs) are the leading cause of
126 Supplementary immunisation activities with oral poliovirus vaccines (OPVs) are usually separated by
127 ssociated paralytic poliomyelitis from Sabin oral poliovirus vaccines (OPVs) has stimulated developme
128 es to estimate the clinical effectiveness of oral poliovirus vaccines (OPVs) in Afghanistan and Pakis
129 of seropositivity was the number of doses of oral poliovirus vaccine received (P < .01), with levels
131 % received the third dose of pentavalent and oral poliovirus vaccine, respectively, but only 65% rece
133 d by this manufacturer to inactivate SV40 in oral poliovirus vaccine seed stocks based on heat inacti
134 r determinants of attenuation of the Sabin 2 oral poliovirus vaccine strain (A481 in the 5'-untransla
135 e (nt 3271 to 3637) derived from the Sabin 1 oral poliovirus vaccine strain spanning the 3'-terminal
136 within the capsid region of the Sabin type 2 oral poliovirus vaccine strain with corresponding nonpre
138 to eradicate poliomyelitis by administering oral poliovirus vaccine through routine immunization and
140 been hampered by low responses to trivalent oral poliovirus vaccine (tOPV) in some developing countr
141 the proposed worldwide switch from trivalent oral poliovirus vaccine (tOPV) to bivalent types 1 and 3
147 osine mutation at nucleotide position 472 of oral poliovirus vaccine type 3 (OPV3) contributes to the
148 Twelve monovalent lots of live, attenuated oral poliovirus vaccine types 1, 2, and 3, which were re
150 type 1 oral poliovirus vaccine and trivalent oral poliovirus vaccine, using the reported number of do
151 ts aged 9-10 months who had already received oral poliovirus vaccine were randomly assigned to receiv
152 opped after multiple vaccination rounds with oral poliovirus vaccine, which targeted the entire popul
153 reviously, we demonstrated the monitoring of oral poliovirus vaccine with the use of mutant analysis
154 ization, the allegations of contamination of oral poliovirus vaccines with human immunodeficiency vir