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The Journal of Clinical Investigation|October 1, 1971
Genetically determined heterogeneity of the C1 esterase inhibitor in patients with hereditary angioneurotic edemaF S Rosen, C A Alper, J Pensky, et al.
The Journal of Clinical Investigation|March 1, 1975
Restoration by purified C3b inactivator of complement-mediated function in vivo in a patient with C3b inactivator deficiencyJ B Ziegler, C A Alper, R S Rosen, et al.
The Journal of Clinical Investigation|November 1, 1970
Studies in vivo and in vitro on an abnormality in the metabolism of C3 in a patient with increased susceptibility to infectionC A Alper, N Abramson, R B Johnston, et al.
The Journal of Clinical Investigation|September 1, 1975
Metabolism of properdin in normal subjects and patients with renal diseaseJ B Ziegler, F S Rosen, C A Alper, et al.
The American Journal of Pathology|September 1, 1976
Nutritional deficiency, immunologic function, and diseaseR A Good, G Fernandes, E J Yunis, et al.
Neurology|January 1, 1980
A family with hereditary ataxia: HLA typingH E Nino, H J Noreen, D P Dubey, et al.
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