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Journal Abstract Search

363 related items for PubMed ID: 21288251

  • 1. Regulatory environment for allergen-specific immunotherapy.
    Kaul S, May S, Lüttkopf D, Vieths S.
    Allergy; 2011 Jun; 66(6):753-64. PubMed ID: 21288251
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  • 8. [Registration of new medicinal products in Europe].
    Singer E.
    Onkologie; 2008 Jun; 31 Suppl 2():64-6. PubMed ID: 18487872
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  • 9. Granting marketing authorisation for medicines in South East European countries: the point of view of the authority.
    Tomić S, Sucić AF, Martinac AI.
    Regul Toxicol Pharmacol; 2010 Jun; 57(2-3):325-32. PubMed ID: 20385190
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  • 12. [Governmental batch sample testing of allergen products].
    Bartel D, Führer F, Vieths S.
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2012 Mar; 55(3):358-62. PubMed ID: 22373849
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  • 15. Regulatory aspects of specific immunotherapy in Europe.
    Kaul S, Englert L, May S, Vieths S.
    Curr Opin Allergy Clin Immunol; 2010 Dec; 10(6):594-602. PubMed ID: 20864886
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  • 18. European Union guidance on the quality, safety and efficacy of DNA vaccines and regulatory requirements.
    Robertson JS, Cichutek K.
    Dev Biol (Basel); 2000 Dec; 104():53-6. PubMed ID: 11713824
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  • 19. Comparison of allergen immunotherapy practice patterns in the United States and Europe.
    Cox L, Jacobsen L.
    Ann Allergy Asthma Immunol; 2009 Dec; 103(6):451-59; quiz 459-61, 495. PubMed ID: 20084837
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  • 20. Understanding differences in allergen immunotherapy products and practices in North America and Europe.
    Mahler V, Esch RE, Kleine-Tebbe J, Lavery WJ, Plunkett G, Vieths S, Bernstein DI.
    J Allergy Clin Immunol; 2019 Mar; 143(3):813-828. PubMed ID: 30850069
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