Congenital bleeding disorders with long bleeding time and normal platelet count. II. Von Willebrand's disease (report of thirty-seven patients).

[1]  R. Haslam,et al.  The adenylate kinase of human plasma, erythrocytes and platelets in relation to the degradation of adenosine diphosphate in plasma. , 1967, The Biochemical journal.

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

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

[4]  J. Caen,et al.  Congenital bleeding disorders with long bleeding time and normal platelet count: I. Glanzmann's thrombasthenia (report of fifteen patients) , 1966 .

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

[6]  T. Spaet,et al.  Studies on Platelet Factor‐3 Availability , 1965, British journal of haematology.

[7]  H. Roberts,et al.  Heterozygosity and Homozygosity in von Willebrand's Disease.∗ , 1965, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[8]  M. Goudemand,et al.  Effet des transfusions de sérum au cours de la maladie de Willebrand. , 1965 .

[9]  H. Roberts,et al.  Possible implications of the autosomal and X-linked hemophilia phenotypes. , 1965, Thrombosis et diathesis haemorrhagica. Supplementum.

[10]  R. Hutton,et al.  THROMBASTHENIA. STUDIES ON THREE CASES. , 1964, British journal of haematology.

[11]  Odegaard Ae,et al.  ADP-INDUCED PLATELET ADHESIVENESS AS A DIAGNOSTIC TEST IN VON WILLEBRAND'S DISEASE. , 1964 .

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

[13]  C. Borchgrevink,et al.  THE HAEMOSTATIC MECHANISM IN PATIENTS WITH HAEMORRHAGIC DISEASES. A HISTOLOGICAL STUDY OF WOUNDS MADE FOR PRIMARY AND SECONDARY BLEEDING TIME TESTS. , 1964, Acta pathologica et microbiologica Scandinavica.

[14]  P. Fantl,et al.  Stimulation of Factor VIII (Antihæmophilic) Activity by Transfused Serum , 1963, Nature.

[15]  H. Strauss,et al.  ELEVATION OF FACTOR VIII (ANTIHEMOPHILIC FACTOR) DURING PREGNANCY IN NORMAL PERSONS AND IN A PATIENT WITH VON WILLEBRAND'S DISEASE. , 1963, The New England journal of medicine.

[16]  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.

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

[18]  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.

[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. Caen.  Ratio Adenosine Triphosphate/Adenosine Diphosphate in Platelet-rich Plasma in Hæmorrhagic Disorders (Von Willebrand and Glanzmann Disease) , 1963, Nature.

[21]  M. Stefanini,et al.  Angiohemophilia: studies in vivo. , 1963, Acta Haematologica.

[22]  O. Egeberg.  The Effect of Muscular Exercise on Hemostasis in Von Willebrand's Disease , 1963 .

[23]  M. Blombäck,et al.  The Use of Human Anti-haemophiiic Globulin (Fraction I-O) in Haemophilia A and in von Willebrand’s Disease , 1960 .

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

[25]  C. Spurling,et al.  Inherited hemorrhagic disorder with antihemophilic globulin deficiency and prolonged bleeding time (vascular hemophilia). , 1959, The New England journal of medicine.

[26]  R. G. Macfarlane,et al.  Haemophilia and Related Conditions: A Survey of 187 Cases , 1958, British journal of haematology.

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

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

[29]  C. Finch,et al.  VASCULAR HEMOPHILIA: THE ASSOCIATION OF A VASCULAR DEFECT WITH A DEFICIENCY OF ANTIHEMOPHILIC GLORULIN* , 1956, American Journal of the Medical Sciences.

[30]  M. Erlandson,et al.  Vascular hemophilia; a familial hemorrhagic disease in males and females characterized by combined antihemophilic globulin deficiency and vascular abnormality. , 1956, Pediatrics.

[31]  B. Ramot,et al.  Pseudohemophilia type B; hereditary hemorrhagic diathesis characterized by prolonged bleeding time and decrease in antihemophilic factor. , 1956, A.M.A. archives of internal medicine.

[32]  B. S. Leavell,et al.  Pseudohemophilia: report of 13 new cases and statistical review of previously reported cases. , 1956, Annals of internal medicine.

[33]  R. Biggs,et al.  The Assay of Antihaemophilic‐Globulin Activity , 1955, British journal of haematology.

[34]  A. S. Douglas,et al.  The Thromboplastin Generation Test , 1953, Journal of clinical pathology.