Treatment of haemophilia A by continuous factor VIII infusion. 1995

T E Hawkins, and G J Green, and K Romeril, and G S Milicich, and J M Carter
Haematology Department, Wellington Hospital, New Zealand.

UI MeSH Term Description Entries
D007263 Infusions, Parenteral The administration of liquid medication, nutrient, or other fluid through some other route than the alimentary canal, usually over minutes or hours, either by gravity flow or often by infusion pumping. Intra-Abdominal Infusions,Intraperitoneal Infusions,Parenteral Infusions,Peritoneal Infusions,Infusion, Intra-Abdominal,Infusion, Intraperitoneal,Infusion, Parenteral,Infusion, Peritoneal,Infusions, Intra-Abdominal,Infusions, Intraperitoneal,Infusions, Peritoneal,Intra Abdominal Infusions,Intra-Abdominal Infusion,Intraperitoneal Infusion,Parenteral Infusion,Peritoneal Infusion
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
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
D000293 Adolescent A person 13 to 18 years of age. Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths

Related Publications

T E Hawkins, and G J Green, and K Romeril, and G S Milicich, and J M Carter
June 1970, British journal of haematology,
T E Hawkins, and G J Green, and K Romeril, and G S Milicich, and J M Carter
September 2016, Blood transfusion = Trasfusione del sangue,
T E Hawkins, and G J Green, and K Romeril, and G S Milicich, and J M Carter
December 1992, British journal of haematology,
T E Hawkins, and G J Green, and K Romeril, and G S Milicich, and J M Carter
May 1999, Haemophilia : the official journal of the World Federation of Hemophilia,
T E Hawkins, and G J Green, and K Romeril, and G S Milicich, and J M Carter
September 2000, British journal of haematology,
T E Hawkins, and G J Green, and K Romeril, and G S Milicich, and J M Carter
September 2002, Haemophilia : the official journal of the World Federation of Hemophilia,
T E Hawkins, and G J Green, and K Romeril, and G S Milicich, and J M Carter
July 2018, Haemophilia : the official journal of the World Federation of Hemophilia,
T E Hawkins, and G J Green, and K Romeril, and G S Milicich, and J M Carter
March 1996, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis,
T E Hawkins, and G J Green, and K Romeril, and G S Milicich, and J M Carter
April 1993, Seminars in hematology,
T E Hawkins, and G J Green, and K Romeril, and G S Milicich, and J M Carter
July 1996, Haemophilia : the official journal of the World Federation of Hemophilia,
Copied contents to your clipboard!