Chido and Rodgers antibodies in haemophiliacs. 1983

R Hussain, and J H Edwards, and C R Rizza, and P Tippett

UI MeSH Term Description Entries
D008297 Male Males
D003181 Complement C4 A glycoprotein that is important in the activation of CLASSICAL COMPLEMENT PATHWAY. C4 is cleaved by the activated COMPLEMENT C1S into COMPLEMENT C4A and COMPLEMENT C4B. C4 Complement,C4 Complement Component,Complement 4,Complement C4, Precursor,Complement Component 4,Pro-C4,Pro-complement 4,C4, Complement,Complement Component, C4,Complement, C4,Component 4, Complement,Component, C4 Complement,Pro C4,Pro complement 4
D005169 Factor VIII Factor VIII of blood coagulation. Antihemophilic factor that is part of the factor VIII/von Willebrand factor complex. Factor VIII is produced in the liver and acts in the intrinsic pathway of blood coagulation. It serves as a cofactor in factor X activation and this action is markedly enhanced by small amounts of thrombin. Coagulation Factor VIII,Factor VIII Clotting Antigen,Factor VIII Coagulant Antigen,Factor VIII Procoagulant Activity,Thromboplastinogen,Blood Coagulation Factor VIII,F VIII-C,Factor 8,Factor 8 C,Factor Eight,Factor VIIIC,Hyate-C,Hyatt-C,F VIII C,Hyate C,HyateC,Hyatt C,HyattC
D006467 Hemophilia A The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage. Factor VIII Deficiency,Hemophilia,Autosomal Hemophilia A,Classic Hemophilia,Deficiency, Factor VIII,Factor 8 Deficiency, Congenital,Factor VIII Deficiency, Congenital,Haemophilia,Hemophilia A, Congenital,Hemophilia, Classic,As, Autosomal Hemophilia,Autosomal Hemophilia As,Classic Hemophilias,Congenital Hemophilia A,Congenital Hemophilia As,Hemophilia A, Autosomal,Hemophilia As,Hemophilia As, Autosomal,Hemophilia As, Congenital,Hemophilias, Classic
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000906 Antibodies Immunoglobulin molecules having a specific amino acid sequence by virtue of which they interact only with the ANTIGEN (or a very similar shape) that induced their synthesis in cells of the lymphoid series (especially PLASMA CELLS).

Related Publications

R Hussain, and J H Edwards, and C R Rizza, and P Tippett
January 1990, Complement and inflammation,
R Hussain, and J H Edwards, and C R Rizza, and P Tippett
December 1979, Transplantation proceedings,
R Hussain, and J H Edwards, and C R Rizza, and P Tippett
January 1988, Experimental and clinical immunogenetics,
R Hussain, and J H Edwards, and C R Rizza, and P Tippett
January 1981, Transfusion,
R Hussain, and J H Edwards, and C R Rizza, and P Tippett
January 2010, Immunohematology,
R Hussain, and J H Edwards, and C R Rizza, and P Tippett
December 1978, Transplantation proceedings,
R Hussain, and J H Edwards, and C R Rizza, and P Tippett
December 2019, Immunohematology,
R Hussain, and J H Edwards, and C R Rizza, and P Tippett
January 1981, Seminars in hematology,
R Hussain, and J H Edwards, and C R Rizza, and P Tippett
January 1994, Immunogenetics,
R Hussain, and J H Edwards, and C R Rizza, and P Tippett
December 1982, Molecular immunology,
Copied contents to your clipboard!