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The Journal of Clinical Investigation|November 1, 1977
Hereditary C7 deficiency. Diagnosis and HLA studies in a French-Canadian familyJ M Delâge, P Bergeron, J Simard, et al.
Immunology|June 1, 1979
Simultaneous occurrence of hereditary C6 and C2 deficiency in a French-Canadian familyJ M Delâge, G Lehner-Netsch, R Lafleur, et al.
Contraception|December 1, 1987
The classical and alternate pathways of complement in oral contraceptive usersJ M Delâge, G Lehner-Netsch, J Brisson
Immunology|October 1, 1976
The enhancement of the haemolytic activity of the first component of complement by trasylolJ M Delage, J Simard, G Lehner-netsch
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 1, 1994
Familial hemolytic-uremic syndrome and homozygous factor H deficiencyV Pichette, S Quérin, W Schürch, et al.
Clinical and Experimental Immunology|January 1, 1982
C3b inactivator deficiency with immune complex manifestationsP Solal-Celigny, M Laviolette, J Hebert, et al.
The Journal of Nutrition, Health & Aging|November 7, 2007
Silent and invisible; nursing home residents with advanced dementiaJ Simard
British Journal of Haematology|June 1, 1997
Multiple bcl-2/Ig gene rearrangements in persistent polyclonal B-cell lymphocytosisR Delage, J Roy, L Jacques, et al.
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