ristocetin and Hemophilia-B

ristocetin has been researched along with Hemophilia-B* in 4 studies

Reviews

2 review(s) available for ristocetin and Hemophilia-B

Article	Year
Familial multiple coagulation factor deficiencies. II. Combined factor VIII, IX, and XI deficiency and combined factor IX and XI deficiency: two previously uncharacterized familial multiple factor deficiency syndromes. Seminars in thrombosis and hemostasis, 1981,Fall, Volume: 7, Issue:2 Topics: Adult; Antigens; Blood Coagulation Disorders; Blood Transfusion; Child; Child, Preschool; Factor V Deficiency; Factor VIII; Factor XI Deficiency; Female; Hemophilia A; Hemophilia B; Humans; Male; Pedigree; Ristocetin; Syndrome	1981
The structure and function of factors VIII and IX. Clinics in haematology, 1979, Volume: 8, Issue:1 Topics: Antibodies; Antigens; Chemical Phenomena; Chemistry; Factor IX; Factor VIII; Hemophilia B; Humans; Ristocetin	1979

Article

Year

Familial multiple coagulation factor deficiencies. II. Combined factor VIII, IX, and XI deficiency and combined factor IX and XI deficiency: two previously uncharacterized familial multiple factor deficiency syndromes.

Seminars in thrombosis and hemostasis, 1981,Fall, Volume: 7, Issue:2

Topics: Adult; Antigens; Blood Coagulation Disorders; Blood Transfusion; Child; Child, Preschool; Factor V Deficiency; Factor VIII; Factor XI Deficiency; Female; Hemophilia A; Hemophilia B; Humans; Male; Pedigree; Ristocetin; Syndrome

1981

The structure and function of factors VIII and IX.

Clinics in haematology, 1979, Volume: 8, Issue:1

Topics: Antibodies; Antigens; Chemical Phenomena; Chemistry; Factor IX; Factor VIII; Hemophilia B; Humans; Ristocetin

1979

Other Studies

2 other study(ies) available for ristocetin and Hemophilia-B

Article	Year
[Thrombocyte aggregation and the secretion reaction in hemophilia patients]. Vutreshni bolesti, 1989, Volume: 28, Issue:2 The action of platelet aggregation and release reaction on the tendency toward bleeding in patients with hemophilia was studied. Were examined 43 patients with hemophilia A, 14 of them with hemorrhages, 5 patients with hemophilia B, 5 patients with hemophilia A and factor VIII inhibitor and 2 patients with congenital factor VII deficit. Disturbed aggregation with ADP was found in 2 patients and with adrenalin also in 2 patients with hemophilia A without hemorrhages, in 1 patient with hemophilia A with hemorrhages and in 1 patient with hemophilia B. In the remaining patients the examined indices were normal. No data for spontaneous aggregation were found. The results of the study indicate that no connection was established between the tendency toward bleeding in the hemophiliac patients and the platelet aggregation and release reaction. No data for platelet hyperactivation by the hemorrhages were found. Topics: Adenosine Diphosphate; Adenosine Triphosphate; Epinephrine; Factor VII Deficiency; Hemophilia A; Hemophilia B; Humans; Platelet Aggregation; Ristocetin	1989
Molecular size distribution of factor VIII in native plasma. Thrombosis research, 1979, Volume: 14, Issue:4-5 Topics: Antigens; Chromatography, Gel; Citrates; Factor VIII; Hemophilia B; Humans; Molecular Weight; Plasma; Ristocetin; Sepharose	1979

Article

Year

[Thrombocyte aggregation and the secretion reaction in hemophilia patients].

Vutreshni bolesti, 1989, Volume: 28, Issue:2

The action of platelet aggregation and release reaction on the tendency toward bleeding in patients with hemophilia was studied. Were examined 43 patients with hemophilia A, 14 of them with hemorrhages, 5 patients with hemophilia B, 5 patients with hemophilia A and factor VIII inhibitor and 2 patients with congenital factor VII deficit. Disturbed aggregation with ADP was found in 2 patients and with adrenalin also in 2 patients with hemophilia A without hemorrhages, in 1 patient with hemophilia A with hemorrhages and in 1 patient with hemophilia B. In the remaining patients the examined indices were normal. No data for spontaneous aggregation were found. The results of the study indicate that no connection was established between the tendency toward bleeding in the hemophiliac patients and the platelet aggregation and release reaction. No data for platelet hyperactivation by the hemorrhages were found.

Topics: Adenosine Diphosphate; Adenosine Triphosphate; Epinephrine; Factor VII Deficiency; Hemophilia A; Hemophilia B; Humans; Platelet Aggregation; Ristocetin

1989

Molecular size distribution of factor VIII in native plasma.

Thrombosis research, 1979, Volume: 14, Issue:4-5

Topics: Antigens; Chromatography, Gel; Citrates; Factor VIII; Hemophilia B; Humans; Molecular Weight; Plasma; Ristocetin; Sepharose

1979