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Experimental and Clinical Immunogenetics|January 1, 1995
Fluorescent detection of microsatellite polymorphisms: properdin deficiency linked to PFC microsatelliteD Agardi, M Pigg, A G Sjöholm, et al.Frontiers in Immunology|January 8, 2015
Is dosing of therapeutic immunoglobulins optimal? A review of a three-decade long debate in europeJacqueline Kerr, Isabella Quinti, Martha Eibl, et al.Clinical and Experimental Immunology|November 11, 1999
Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n)P J Späth, A G Sjöholm, G N Fredrikson, et al.Pain Medicine (Malden, Mass.)|January 16, 2014
Immunoglobulin g for the treatment of chronic pain: report of an expert workshopStefano Tamburin, Kristian Borg, Xavier J Caro, et al.Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|January 29, 2008
Hereditary angiodema: a current state-of-the-art review, VII: Canadian Hungarian 2007 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary AngioedemaTom Bowen, Marco Cicardi, Konrad Bork, et al.The Journal of Allergy and Clinical Immunology|September 10, 2004
Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyondAngelo Agostoni, Emel Aygören-Pürsün, Karen E Binkley, et al.Pageof 7