Factor-VIII levels, bleeding-times, and platelet adhesiveness in patients with Von Willebrand's disease and in their relatives.

[1]  J. Wood,et al.  A new abnormality of platelet function. , 1970, Acta haematologica.

[2]  D. Meyer,et al.  Von Willebrand factor and platelet adhesiveness , 1970, Journal of clinical pathology.

[3]  P. Didisheim,et al.  Platelet adhesiveness in von Willebrand's disease. , 1969, American journal of clinical pathology.

[4]  H. Weiss.  Analytic Review: Von Willebrand’s Disease-Diagnostic Criteria , 1968 .

[5]  Y. Sultan,et al.  Congenital bleeding disorders with long bleeding time and normal platelet count. II. Von Willebrand's disease (report of thirty-seven patients). , 1968, The American journal of medicine.

[6]  H. Weiss.  Platelet aggregation, adhesion and adenosine diphosphate release in thrombopathia (platelet factor 3 deficiency). A comparison with Glanzmann's thrombasthenia and von Willebrand's disease. , 1967, The American journal of medicine.

[7]  H. Perkins.  Brief Report: Correction of the Hemostatic Defects in Von Willebrand’s Disease , 1967 .

[8]  D. Meyer,et al.  Biological findings in Von Willebrand's pedigrees: implications for inheritance , 1967, Journal of clinical pathology.

[9]  J. Heywood,et al.  Some interactions between human platelets and glass: von Willebrand's disease compared with normal , 1967, Journal of clinical pathology.

[10]  K. Dormandy,et al.  Pool's cryoprecipitate and exhausted plasma in the treatment of von Willebrand's disease and factor-XI deficiency. , 1966, Lancet.

[11]  H. Strauss,et al.  VON WILLEBRAND'S DISEASE: USE OF A PLATELET-ADHESIVENESS TEST IN DIAGNOSIS AND FAMILY INVESTIGATION. , 1965 .

[12]  J. Caen,et al.  A useful photometric test for the diagnosis of Von Willebrand's disease , 1964, Journal of clinical pathology.

[13]  H. Roberts,et al.  Studies of the Antihemophilic Factor (AHF, Factor VIII) Produced in von Willebrand's Disease.∗ , 1964, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[14]  H. Weiss,et al.  SECONDARY THROMBOCYTOPATHIA. PLATELET FACTOR 3 IN VARIOUS DISEASE STATES. , 1963, Archives of internal medicine.

[15]  E. Salzman.  MEASUREMENT OF PLATELET ADHESIVENESS. A SIMPLE IN VITRO TECHNIQUE DEMONSTRATING AN ABNORMALITY IN VON WILLEBRAND'S DISEASE. , 1963, The Journal of laboratory and clinical medicine.

[16]  J. Caen,et al.  Transfusion Studies in von Willebrand's Disease: Effect on Bleeding Time and Factor VIII , 1963, British journal of haematology.

[17]  R. Biggs,et al.  The Treatment of Haemorrhage in von Willebrand's Disease and the Blood Level of Factor VIII (AHG) , 1963, British journal of haematology.

[18]  J. Graham,et al.  Synthesis of Plasma Antihæmophilic Factor , 1963, Nature.

[19]  M. B. Zucker,et al.  In vitro Abnormality of the Blood in Von Willebrand's Disease correctable by Normal Plasma , 1963, Nature.

[20]  J. R. O'brien.  Platelet aggregation , 1962, Journal of clinical pathology.

[21]  G. Born,et al.  Aggregation of Blood Platelets by Adenosine Diphosphate and its Reversal , 1962, Nature.

[22]  I. Nilsson,et al.  v. Willebrand's disease in Sweden; its pathogenesis and treatment. , 2009, Acta medica Scandinavica.

[23]  J. Graham.  The Inheritance of "Vascular Hemophilia": A New and Interesting Problem in Human Genetics. , 1959, American journal of human genetics.

[24]  M. Blombäck,et al.  On an inherited autosomal hemorrhagic diathesis with antihemophilic globulin (AHG) deficiency and prolonged bleeding time. , 2009, Acta medica Scandinavica.

[25]  I. Nilsson,et al.  Von Willebrand's disease and its correction with human plasma fraction 1-0. , 2009, Acta medica Scandinavica.

[26]  R. Macfarlane.  A SIMPLE METHOD FOR MEASURING CLOT-RETRACTION , 1939 .