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Safety, immunogenicity, and efficacy of quadrivalent human papillomavirus (types 6, 11, 16, 18) recombinant vaccine in women aged 24—45 years: a randomised, double-blind trial
The Lancet, 06/08/09
Munoz N et al. - Although the peak incidence of human papillomavirus (HPV) infection occurs in most populations within 5—10 years of first sexual experience, all women remain at risk for acquisition of HPV infections. The authors tested the safety, immunogenicity, and efficacy of the quadrivalent HPV (types 6, 11, 16, 18) L1 virus-like-particle vaccine in women aged 24—45 years. The quadrivalent HPV vaccine is efficacious in women aged 24—45 years not infected with the relevant HPV types at enrolment.
Today in Sexually Transmitted Dz...keeping you current
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Human papillomavirus vaccination in survivors of childhood cancer
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Factors Determining Serologic Response to Treatment in Patients with Syphilis
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Sexual orientation in males and the evolution of anisogamy
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FDA Approves Gardasil to Prevent Genital Warts in Males. Agency Also Approves Bivalent HPV Vaccine for Girls, Young Women
American Family Physician, 10/21/09
HPV: Past, present, and in practice: The Omnia CME Journal
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New England Journal of Medicine, 10/29/09
Today in Vaccine/Immunotherapy...keeping you current
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FDA Approves Gardasil to Prevent Genital Warts in Males. Agency Also Approves Bivalent HPV Vaccine for Girls, Young Women
American Family Physician, 10/21/09
Update on vaccination guidelines for allergic children
Expert Review of Vaccines, 10/29/09
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International Journal of Epidemiology, 10/14/09
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