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1 V13) was introduced to the routine childhood immunization schedule.
2 ecently incorporated into the United Kingdom immunization schedule.
3 ate vaccine (MCCV) into their routine infant immunization schedule.
4 h titers increasing progressively during the immunization schedule.
5 s PCV7 was being introduced into the routine immunization schedule.
6 FP-specific humoral responses using the same immunization schedule.
7 vaccine on the United Kingdom's 2/3/4-month immunization schedule.
8 ivery by using a parenteral prime-oral boost immunization schedule.
9 ltiple-injection visits included in national immunization schedules.
10 cines included in the 2010 annual harmonized immunization schedules.
11 de introduction of RCV in national childhood immunization schedules.
12 ldhood when incorporated into routine infant immunization schedules.
13 otein B (CMV gB)/MF59 vaccine at 3 different immunization schedules.
14 alent IPV or combined vaccines for childhood immunization schedules.
15 g 2013-2015, 85 countries added IPV to their immunization schedules, 46 (55%) of which adopted a sche
16 mpliance with the recommended 2-dose measles immunization schedule, 6% of high school students were s
19 e Country, where neonatal BCG is part of the immunization schedule and has a 100% coverage) as compar
20 rapidly introduced into the Alaska childhood immunization schedule and reduced colonization by PCV6+
21 e of vaccine, but we evaluated two different immunization schedules and the oropharyngeal and intrana
22 rning neonatal herpes infections, poliovirus immunization schedule, and group B streptococcus screeni
24 inactivated poliovirus vaccine into routine immunization schedules, and it describes the proposed im
25 hat did not yet include it in their national immunization schedules, and to "switch" from trivalent O
28 ing a single IPV dose to an OPV-only routine immunization schedule at or just before OPV cessation pr
29 bias may become more likely in the future as immunization schedules become more complex and variable.
33 table vaccines delivered through the routine immunization schedule: diphtheria-tetanus-pertussis vacc
34 ng of maternal protection and routine infant immunization schedules, exacerbated by the failure of va
35 f varicella vaccine was added to the routine immunization schedule for children in June 2006 by the C
36 care professionals may not conform to proper immunization schedules for premature and low-birth-weigh
37 cts received placebo, 13 received a complete immunization schedule (> or = 3 injections), and 6 were
39 ugate vaccine (PCV7) into the U.S. childhood immunization schedule in 2000 has substantially reduced
40 Introduction of PCV7 into the routine infant immunization schedule in a community with a high prevale
43 ugate vaccine (PCV7) into the routine infant immunization schedule in England, Wales, and Northern Ir
44 vaccination was introduced into the routine immunization schedule in the United States in late 2006
45 ion of at least one dose of IPV into routine immunization schedules in 126 all OPV-using countries by
47 ebec, Canada, where a routine 2-dose measles immunization schedule, in which measles vaccine is given
53 mumps-rubella-varicella (MMRV) vaccine, into immunization schedules should be evaluated from a benefi
54 ntaining vaccines in their routine childhood immunization schedules, supported through the Expanded P
55 cine and subsequent switch to their national immunization schedules.The purpose of this article is to
57 present two-dose measles-mumps-rubella (MMR) immunization schedule to one-dose of MMR; second, the us
58 assays provide an opportunity to study other immunization schedules to gain a broader understanding o
59 how a greater differential response to the 2 immunization schedules used in this study suggests that
60 e regimen, in which the standard 0-1-2 month immunization schedule was modified to a 0-1-7 month sche
61 aRT plus IFN-gamma and IFN-gamma alone), the immunization schedule was reduced to 0, 4, and 8 weeks.
62 included in the current Expanded Program on Immunization schedule, we estimated the reduction in rot
63 tion of the varicella vaccine to the routine immunization schedule, we have observed a 70% reduction
64 r optimization in vaccine composition and/or immunization schedule will be required to induce longer-
65 future control of B. pertussis will require immunization schedules with new acellular vaccines that
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