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M M Frank

Showing results (151-160 of 288) with videos related to

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The Journal of Clinical Investigation|July 1, 1979
Response of variant hereditary angioedema phenotypes to danazol therapy. Genetic implicationsJ E Gadek, S W Hosea, J A Gelfand, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 15, 1987
Modulation of FcR function by complement: subcomponent C1q enhances the phagocytosis of IgG-opsonized targets by human monocytes and culture-derived macrophagesD A Bobak, T A Gaither, M M Frank, et al.
The Journal of Allergy and Clinical Immunology|June 1, 1975
Hereditary angioedema: the use of fresh frozen plasma for prophylaxis in patients undergoing oral surgeryC J Jaffe, J P Atkinson, J A Gelfand, et al.
The American Journal of Medicine|January 1, 1975
Hereditary complement (C2) deficiency with dermatomyositisJ P Leddy, R C Griggs, M R Klemperer, et al.
The Journal of Infectious Diseases|January 1, 1975
Serum complement and immunity in experimental simian malaria. II. Preferential activation of early components and failure of depletion of late components to inhibit protective immunityJ P Atkinson, R H Glew, F A Neva, et al.
Transactions of the Association of American Physicians|January 1, 1976
The effect of synthetic androgens in hereditary angioneurotic edema: alteration of C1 inhibitor and C4 levelsW F Rosse, G L Logue, H R Silberman, et al.
The Journal of Experimental Medicine|December 1, 1984
C3b covalently bound to IgG demonstrates a reduced rate of inactivation by factors H and IL F Fries, T A Gaither, C H Hammer, et al.
Annals of Internal Medicine|October 1, 1979
Sjögren's syndrome: a defect in reticuloendothelial system Fc-receptor-specific clearanceM I Hamburger, H M Moutsopoulos, T J Lawley, et al.
The New England Journal of Medicine|April 13, 1972
Epsilon aminocaproic acid therapy of hereditary angioneurotic edema. A double-blind studyM M Frank, J S Sergent, M A Kane, et al.
The New England Journal of Medicine|July 22, 1976
Endotoxemia associated with the Jarisch-Herxheimer reactionJ A Gelfand, R J Elin, F W Berry, et al.
Pageof 29

Showing results (151-160 of 288) with videos related to

Sort By:
Pageof 29
The Journal of Clinical Investigation|July 1, 1979
Response of variant hereditary angioedema phenotypes to danazol therapy. Genetic implicationsJ E Gadek, S W Hosea, J A Gelfand, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 15, 1987
Modulation of FcR function by complement: subcomponent C1q enhances the phagocytosis of IgG-opsonized targets by human monocytes and culture-derived macrophagesD A Bobak, T A Gaither, M M Frank, et al.
The Journal of Allergy and Clinical Immunology|June 1, 1975
Hereditary angioedema: the use of fresh frozen plasma for prophylaxis in patients undergoing oral surgeryC J Jaffe, J P Atkinson, J A Gelfand, et al.
The American Journal of Medicine|January 1, 1975
Hereditary complement (C2) deficiency with dermatomyositisJ P Leddy, R C Griggs, M R Klemperer, et al.
The Journal of Infectious Diseases|January 1, 1975
Serum complement and immunity in experimental simian malaria. II. Preferential activation of early components and failure of depletion of late components to inhibit protective immunityJ P Atkinson, R H Glew, F A Neva, et al.
Transactions of the Association of American Physicians|January 1, 1976
The effect of synthetic androgens in hereditary angioneurotic edema: alteration of C1 inhibitor and C4 levelsW F Rosse, G L Logue, H R Silberman, et al.
The Journal of Experimental Medicine|December 1, 1984
C3b covalently bound to IgG demonstrates a reduced rate of inactivation by factors H and IL F Fries, T A Gaither, C H Hammer, et al.
Annals of Internal Medicine|October 1, 1979
Sjögren's syndrome: a defect in reticuloendothelial system Fc-receptor-specific clearanceM I Hamburger, H M Moutsopoulos, T J Lawley, et al.
The New England Journal of Medicine|April 13, 1972
Epsilon aminocaproic acid therapy of hereditary angioneurotic edema. A double-blind studyM M Frank, J S Sergent, M A Kane, et al.
The New England Journal of Medicine|July 22, 1976
Endotoxemia associated with the Jarisch-Herxheimer reactionJ A Gelfand, R J Elin, F W Berry, et al.
Pageof 29