Zobrazeno 1 - 10
of 499
pro vyhledávání: '"M. J. Larrieu"'
Publikováno v:
Scandinavian Journal of Haematology. 28:233-237
Washed red blood cells (WRC) have been used for replacing the blood loss in haemophilia A patients with antibody to Factor VIII. Levels of VIII coagulant activity (VIII:C), VIII coagulant antigen (VIII:CAg) and VIII related antigen (VIIIR:Ag) have be
Publikováno v:
British Journal of Haematology. 50:531-535
Antithrombin III concentrates were administered to a patient with hereditary AT III deficiency undergoing orthopaedic surgery. The plasma AT III level (heparin cofactor activity) was maintained at values in excess of 100% postoperatively. A mean dose
Publikováno v:
Blood Coagulation & Fibrinolysis. 4:679-687
Autor:
Rowland, Grace E.1 (AUTHOR), Purcell, Juliann B.1,2 (AUTHOR), Lebois, Lauren A. M.1,2 (AUTHOR), Kaufman, Milissa L.1,2 (AUTHOR), Harnett, Nathaniel G.1,2 (AUTHOR) nharnett@mclean.harvard.edu
Publikováno v:
Mental Health Science. Jun2024, Vol. 2 Issue 2, p1-15. 15p.
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 4(5)
The aim of this study was to investigate the interactions of t-PA and plasminogen with fibrin derived from an abnormal fibrinogen detected in a 40-year-old male patient who had had an episode of thrombophlebitis with pulmonary embolism. An abnormal f
Publikováno v:
Thrombosis and haemostasis. 63(2)
The association of a variant of antithrombin III (AT III Bligny) and protein C deficiency is described in a 36-year-old patient having suffered from severe thrombotic episodes. His mother has protein C deficiency and showed a single episode of thromb
Publikováno v:
Nouvelle revue francaise d'hematologie. 32(2)
A prenatal diagnosis for fetal disease was performed at 20 weeks gestation in a severely affected patient with type IIA von Willebrand disease. In the fetal cord blood sample obtained under ultrasound guidance, the level of von Willebrand ristocetin
Publikováno v:
Journal of Clinical Pathology. 28:690-695
Factor VIII activity and factor VIII related--or Willebrand--antigen were studied in 49 known carriers of haemophilia A and 31 normal women, and the data were analysed by four statistical approaches. Sixteen per cent of normals and 18% of carriers we
Publikováno v:
The Journal of Bone & Joint Surgery. 69:264-269
Synovectomy of twenty-three elbows was done in eighteen patients, eight to twenty-five years old, who had severe hemophilia and were followed for eighteen to seventy months. Episodes of bleeding recurred in four elbows, and moderate pain persisted in
Publikováno v:
Blood. 65:496-500
A qualitative defect of antithrombin III (AT III) has been demonstrated over three generations in eight members of an Italian family by the discrepancy between a normal amount of antigen and decreased antithrombin and anti-Xa activity in the presence